---
_id: '13352'
abstract:
- lang: eng
  text: Optoelectronic effects differentiating absorption of right and left circularly
    polarized photons in thin films of chiral materials are typically prohibitively
    small for their direct photocurrent observation. Chiral metasurfaces increase
    the electronic sensitivity to circular polarization, but their out-of-plane architecture
    entails manufacturing and performance trade-offs. Here, we show that nanoporous
    thin films of chiral nanoparticles enable high sensitivity to circular polarization
    due to light-induced polarization-dependent ion accumulation at nanoparticle interfaces.
    Self-assembled multilayers of gold nanoparticles modified with L-phenylalanine
    generate a photocurrent under right-handed circularly polarized light as high
    as 2.41 times higher than under left-handed circularly polarized light. The strong
    plasmonic coupling between the multiple nanoparticles producing planar chiroplasmonic
    modes facilitates the ejection of electrons, whose entrapment at the membrane–electrolyte
    interface is promoted by a thick layer of enantiopure phenylalanine. Demonstrated
    detection of light ellipticity with equal sensitivity at all incident angles mimics
    phenomenological aspects of polarization vision in marine animals. The simplicity
    of self-assembly and sensitivity of polarization detection found in optoionic
    membranes opens the door to a family of miniaturized fluidic devices for chiral
    photonics.
article_processing_charge: No
article_type: original
author:
- first_name: Jiarong
  full_name: Cai, Jiarong
  last_name: Cai
- first_name: Wei
  full_name: Zhang, Wei
  last_name: Zhang
- first_name: Liguang
  full_name: Xu, Liguang
  last_name: Xu
- first_name: Changlong
  full_name: Hao, Changlong
  last_name: Hao
- first_name: Wei
  full_name: Ma, Wei
  last_name: Ma
- first_name: Maozhong
  full_name: Sun, Maozhong
  last_name: Sun
- first_name: Xiaoling
  full_name: Wu, Xiaoling
  last_name: Wu
- first_name: Xian
  full_name: Qin, Xian
  last_name: Qin
- first_name: Felippe Mariano
  full_name: Colombari, Felippe Mariano
  last_name: Colombari
- first_name: André Farias
  full_name: de Moura, André Farias
  last_name: de Moura
- first_name: Jiahui
  full_name: Xu, Jiahui
  last_name: Xu
- first_name: Mariana Cristina
  full_name: Silva, Mariana Cristina
  last_name: Silva
- first_name: Evaldo Batista
  full_name: Carneiro-Neto, Evaldo Batista
  last_name: Carneiro-Neto
- first_name: Weverson Rodrigues
  full_name: Gomes, Weverson Rodrigues
  last_name: Gomes
- first_name: Renaud A. L.
  full_name: Vallée, Renaud A. L.
  last_name: Vallée
- first_name: Ernesto Chaves
  full_name: Pereira, Ernesto Chaves
  last_name: Pereira
- first_name: Xiaogang
  full_name: Liu, Xiaogang
  last_name: Liu
- first_name: Chuanlai
  full_name: Xu, Chuanlai
  last_name: Xu
- first_name: Rafal
  full_name: Klajn, Rafal
  id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b
  last_name: Klajn
- first_name: Nicholas A.
  full_name: Kotov, Nicholas A.
  last_name: Kotov
- first_name: Hua
  full_name: Kuang, Hua
  last_name: Kuang
citation:
  ama: Cai J, Zhang W, Xu L, et al. Polarization-sensitive optoionic membranes from
    chiral plasmonic nanoparticles. <i>Nature Nanotechnology</i>. 2022;17(4):408-416.
    doi:<a href="https://doi.org/10.1038/s41565-022-01079-3">10.1038/s41565-022-01079-3</a>
  apa: Cai, J., Zhang, W., Xu, L., Hao, C., Ma, W., Sun, M., … Kuang, H. (2022). Polarization-sensitive
    optoionic membranes from chiral plasmonic nanoparticles. <i>Nature Nanotechnology</i>.
    Springer Nature. <a href="https://doi.org/10.1038/s41565-022-01079-3">https://doi.org/10.1038/s41565-022-01079-3</a>
  chicago: Cai, Jiarong, Wei Zhang, Liguang Xu, Changlong Hao, Wei Ma, Maozhong Sun,
    Xiaoling Wu, et al. “Polarization-Sensitive Optoionic Membranes from Chiral Plasmonic
    Nanoparticles.” <i>Nature Nanotechnology</i>. Springer Nature, 2022. <a href="https://doi.org/10.1038/s41565-022-01079-3">https://doi.org/10.1038/s41565-022-01079-3</a>.
  ieee: J. Cai <i>et al.</i>, “Polarization-sensitive optoionic membranes from chiral
    plasmonic nanoparticles,” <i>Nature Nanotechnology</i>, vol. 17, no. 4. Springer
    Nature, pp. 408–416, 2022.
  ista: Cai J, Zhang W, Xu L, Hao C, Ma W, Sun M, Wu X, Qin X, Colombari FM, de Moura
    AF, Xu J, Silva MC, Carneiro-Neto EB, Gomes WR, Vallée RAL, Pereira EC, Liu X,
    Xu C, Klajn R, Kotov NA, Kuang H. 2022. Polarization-sensitive optoionic membranes
    from chiral plasmonic nanoparticles. Nature Nanotechnology. 17(4), 408–416.
  mla: Cai, Jiarong, et al. “Polarization-Sensitive Optoionic Membranes from Chiral
    Plasmonic Nanoparticles.” <i>Nature Nanotechnology</i>, vol. 17, no. 4, Springer
    Nature, 2022, pp. 408–16, doi:<a href="https://doi.org/10.1038/s41565-022-01079-3">10.1038/s41565-022-01079-3</a>.
  short: J. Cai, W. Zhang, L. Xu, C. Hao, W. Ma, M. Sun, X. Wu, X. Qin, F.M. Colombari,
    A.F. de Moura, J. Xu, M.C. Silva, E.B. Carneiro-Neto, W.R. Gomes, R.A.L. Vallée,
    E.C. Pereira, X. Liu, C. Xu, R. Klajn, N.A. Kotov, H. Kuang, Nature Nanotechnology
    17 (2022) 408–416.
date_created: 2023-08-01T09:32:40Z
date_published: 2022-03-14T00:00:00Z
date_updated: 2023-08-02T09:44:31Z
day: '14'
doi: 10.1038/s41565-022-01079-3
extern: '1'
external_id:
  pmid:
  - '35288671'
intvolume: '        17'
issue: '4'
keyword:
- Electrical and Electronic Engineering
- Condensed Matter Physics
- General Materials Science
- Biomedical Engineering
- Atomic and Molecular Physics
- and Optics
- Bioengineering
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://hal.science/hal-03623036/
month: '03'
oa: 1
oa_version: Published Version
page: 408-416
pmid: 1
publication: Nature Nanotechnology
publication_identifier:
  eissn:
  - 1748-3395
  issn:
  - 1748-3387
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Polarization-sensitive optoionic membranes from chiral plasmonic nanoparticles
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 17
year: '2022'
...
---
_id: '13353'
abstract:
- lang: eng
  text: We show that the optical properties of indigo carmine can be modulated by
    encapsulation within a coordination cage. Depending on the host/guest molar ratio,
    the cage can predominantly encapsulate either one or two dye molecules. The 1 : 1
    complex is fluorescent, unique for an indigo dye in an aqueous solution. We have
    also found that binding two dye molecules stabilizes a previously unknown conformation
    of the cage.
article_processing_charge: No
article_type: original
author:
- first_name: Oksana
  full_name: Yanshyna, Oksana
  last_name: Yanshyna
- first_name: Liat
  full_name: Avram, Liat
  last_name: Avram
- first_name: Linda J. W.
  full_name: Shimon, Linda J. W.
  last_name: Shimon
- first_name: Rafal
  full_name: Klajn, Rafal
  id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b
  last_name: Klajn
citation:
  ama: Yanshyna O, Avram L, Shimon LJW, Klajn R. Coexistence of 1:1 and 2:1 inclusion
    complexes of indigo carmine. <i>Chemical Communications</i>. 2022;58(21):3461-3464.
    doi:<a href="https://doi.org/10.1039/d1cc07081a">10.1039/d1cc07081a</a>
  apa: Yanshyna, O., Avram, L., Shimon, L. J. W., &#38; Klajn, R. (2022). Coexistence
    of 1:1 and 2:1 inclusion complexes of indigo carmine. <i>Chemical Communications</i>.
    Royal Society of Chemistry. <a href="https://doi.org/10.1039/d1cc07081a">https://doi.org/10.1039/d1cc07081a</a>
  chicago: Yanshyna, Oksana, Liat Avram, Linda J. W. Shimon, and Rafal Klajn. “Coexistence
    of 1:1 and 2:1 Inclusion Complexes of Indigo Carmine.” <i>Chemical Communications</i>.
    Royal Society of Chemistry, 2022. <a href="https://doi.org/10.1039/d1cc07081a">https://doi.org/10.1039/d1cc07081a</a>.
  ieee: O. Yanshyna, L. Avram, L. J. W. Shimon, and R. Klajn, “Coexistence of 1:1
    and 2:1 inclusion complexes of indigo carmine,” <i>Chemical Communications</i>,
    vol. 58, no. 21. Royal Society of Chemistry, pp. 3461–3464, 2022.
  ista: Yanshyna O, Avram L, Shimon LJW, Klajn R. 2022. Coexistence of 1:1 and 2:1
    inclusion complexes of indigo carmine. Chemical Communications. 58(21), 3461–3464.
  mla: Yanshyna, Oksana, et al. “Coexistence of 1:1 and 2:1 Inclusion Complexes of
    Indigo Carmine.” <i>Chemical Communications</i>, vol. 58, no. 21, Royal Society
    of Chemistry, 2022, pp. 3461–64, doi:<a href="https://doi.org/10.1039/d1cc07081a">10.1039/d1cc07081a</a>.
  short: O. Yanshyna, L. Avram, L.J.W. Shimon, R. Klajn, Chemical Communications 58
    (2022) 3461–3464.
date_created: 2023-08-01T09:32:55Z
date_published: 2022-01-22T00:00:00Z
date_updated: 2023-08-02T09:46:51Z
day: '22'
doi: 10.1039/d1cc07081a
extern: '1'
external_id:
  pmid:
  - '35064258'
intvolume: '        58'
issue: '21'
keyword:
- Materials Chemistry
- Metals and Alloys
- Surfaces
- Coatings and Films
- General Chemistry
- Ceramics and Composites
- Electronic
- Optical and Magnetic Materials
- Catalysis
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1039/D1CC07081A
month: '01'
oa: 1
oa_version: Published Version
page: 3461-3464
pmid: 1
publication: Chemical Communications
publication_identifier:
  eissn:
  - 1364-548X
  issn:
  - 1359-7345
publication_status: published
publisher: Royal Society of Chemistry
quality_controlled: '1'
scopus_import: '1'
status: public
title: Coexistence of 1:1 and 2:1 inclusion complexes of indigo carmine
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 58
year: '2022'
...
---
_id: '13355'
abstract:
- lang: eng
  text: 'Supramolecular self-assembly in biological systems holds promise to convert
    and amplify disease-specific signals to physical or mechanical signals that can
    direct cell fate. However, it remains challenging to design physiologically stable
    self-assembling systems that demonstrate tunable and predictable behavior. Here,
    the use of zwitterionic tetrapeptide modalities to direct nanoparticle assembly
    under physiological conditions is reported. The self-assembly of gold nanoparticles
    can be activated by enzymatic unveiling of surface-bound zwitterionic tetrapeptides
    through matrix metalloprotease-9 (MMP-9), which is overexpressed by cancer cells.
    This robust nanoparticle assembly is achieved by multivalent, self-complementary
    interactions of the zwitterionic tetrapeptides. In cancer cells that overexpress
    MMP-9, the nanoparticle assembly process occurs near the cell membrane and causes
    size-induced selection of cellular uptake mechanism, resulting in diminished cell
    growth. The enzyme responsiveness, and therefore, indirectly, the uptake route
    of the system can be programmed by customizing the peptide sequence: a simple
    inversion of the two amino acids at the cleavage site completely inactivates the
    enzyme responsiveness, self-assembly, and consequently changes the endocytic pathway.
    This robust self-complementary, zwitterionic peptide design demonstrates the use
    of enzyme-activated electrostatic side-chain patterns as powerful and customizable
    peptide modalities to program nanoparticle self-assembly and alter cellular response
    in biological context.'
article_number: '2104962'
article_processing_charge: No
article_type: original
author:
- first_name: Richard H.
  full_name: Huang, Richard H.
  last_name: Huang
- first_name: Nazia
  full_name: Nayeem, Nazia
  last_name: Nayeem
- first_name: Ye
  full_name: He, Ye
  last_name: He
- first_name: Jorge
  full_name: Morales, Jorge
  last_name: Morales
- first_name: Duncan
  full_name: Graham, Duncan
  last_name: Graham
- first_name: Rafal
  full_name: Klajn, Rafal
  id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b
  last_name: Klajn
- first_name: Maria
  full_name: Contel, Maria
  last_name: Contel
- first_name: Stephen
  full_name: O'Brien, Stephen
  last_name: O'Brien
- first_name: Rein V.
  full_name: Ulijn, Rein V.
  last_name: Ulijn
citation:
  ama: Huang RH, Nayeem N, He Y, et al. Self‐complementary zwitterionic peptides direct
    nanoparticle assembly and enable enzymatic selection of endocytic pathways. <i>Advanced
    Materials</i>. 2022;34(1). doi:<a href="https://doi.org/10.1002/adma.202104962">10.1002/adma.202104962</a>
  apa: Huang, R. H., Nayeem, N., He, Y., Morales, J., Graham, D., Klajn, R., … Ulijn,
    R. V. (2022). Self‐complementary zwitterionic peptides direct nanoparticle assembly
    and enable enzymatic selection of endocytic pathways. <i>Advanced Materials</i>.
    Wiley. <a href="https://doi.org/10.1002/adma.202104962">https://doi.org/10.1002/adma.202104962</a>
  chicago: Huang, Richard H., Nazia Nayeem, Ye He, Jorge Morales, Duncan Graham, Rafal
    Klajn, Maria Contel, Stephen O’Brien, and Rein V. Ulijn. “Self‐complementary Zwitterionic
    Peptides Direct Nanoparticle Assembly and Enable Enzymatic Selection of Endocytic
    Pathways.” <i>Advanced Materials</i>. Wiley, 2022. <a href="https://doi.org/10.1002/adma.202104962">https://doi.org/10.1002/adma.202104962</a>.
  ieee: R. H. Huang <i>et al.</i>, “Self‐complementary zwitterionic peptides direct
    nanoparticle assembly and enable enzymatic selection of endocytic pathways,” <i>Advanced
    Materials</i>, vol. 34, no. 1. Wiley, 2022.
  ista: Huang RH, Nayeem N, He Y, Morales J, Graham D, Klajn R, Contel M, O’Brien
    S, Ulijn RV. 2022. Self‐complementary zwitterionic peptides direct nanoparticle
    assembly and enable enzymatic selection of endocytic pathways. Advanced Materials.
    34(1), 2104962.
  mla: Huang, Richard H., et al. “Self‐complementary Zwitterionic Peptides Direct
    Nanoparticle Assembly and Enable Enzymatic Selection of Endocytic Pathways.” <i>Advanced
    Materials</i>, vol. 34, no. 1, 2104962, Wiley, 2022, doi:<a href="https://doi.org/10.1002/adma.202104962">10.1002/adma.202104962</a>.
  short: R.H. Huang, N. Nayeem, Y. He, J. Morales, D. Graham, R. Klajn, M. Contel,
    S. O’Brien, R.V. Ulijn, Advanced Materials 34 (2022).
date_created: 2023-08-01T09:33:26Z
date_published: 2022-01-06T00:00:00Z
date_updated: 2023-08-07T09:58:17Z
day: '06'
doi: 10.1002/adma.202104962
extern: '1'
external_id:
  pmid:
  - '34668253'
intvolume: '        34'
issue: '1'
keyword:
- Mechanical Engineering
- Mechanics of Materials
- General Materials Science
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1002/adma.202104962
month: '01'
oa: 1
oa_version: Published Version
pmid: 1
publication: Advanced Materials
publication_identifier:
  eissn:
  - 1521-4095
  issn:
  - 0935-9648
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: Self‐complementary zwitterionic peptides direct nanoparticle assembly and enable
  enzymatic selection of endocytic pathways
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 34
year: '2022'
...
---
_id: '13991'
abstract:
- lang: eng
  text: The prediction and realization of topological insulators have sparked great
    interest in experimental approaches to the classification of materials1,2,3. The
    phase transition between non-trivial and trivial topological states is important,
    not only for basic materials science but also for next-generation technology,
    such as dissipation-free electronics4. It is therefore crucial to develop advanced
    probes that are suitable for a wide range of samples and environments. Here we
    demonstrate that circularly polarized laser-field-driven high-harmonic generation
    is distinctly sensitive to the non-trivial and trivial topological phases in the
    prototypical three-dimensional topological insulator bismuth selenide5. The phase
    transition is chemically initiated by reducing the spin–orbit interaction strength
    through the substitution of bismuth with indium atoms6,7. We find strikingly different
    high-harmonic responses of trivial and non-trivial topological surface states
    that manifest themselves as a conversion efficiency and elliptical dichroism that
    depend both on the driving laser ellipticity and the crystal orientation. The
    origins of the anomalous high-harmonic response are corroborated by calculations
    using the semiconductor optical Bloch equations with pairs of surface and bulk
    bands. As a purely optical approach, this method offers sensitivity to the electronic
    structure of the material, including its nonlinear response, and is compatible
    with a wide range of samples and sample environments.
article_processing_charge: No
article_type: original
author:
- first_name: Christian
  full_name: Heide, Christian
  last_name: Heide
- first_name: Yuki
  full_name: Kobayashi, Yuki
  last_name: Kobayashi
- first_name: Denitsa Rangelova
  full_name: Baykusheva, Denitsa Rangelova
  id: 71b4d059-2a03-11ee-914d-dfa3beed6530
  last_name: Baykusheva
- first_name: Deepti
  full_name: Jain, Deepti
  last_name: Jain
- first_name: Jonathan A.
  full_name: Sobota, Jonathan A.
  last_name: Sobota
- first_name: Makoto
  full_name: Hashimoto, Makoto
  last_name: Hashimoto
- first_name: Patrick S.
  full_name: Kirchmann, Patrick S.
  last_name: Kirchmann
- first_name: Seongshik
  full_name: Oh, Seongshik
  last_name: Oh
- first_name: Tony F.
  full_name: Heinz, Tony F.
  last_name: Heinz
- first_name: David A.
  full_name: Reis, David A.
  last_name: Reis
- first_name: Shambhu
  full_name: Ghimire, Shambhu
  last_name: Ghimire
citation:
  ama: Heide C, Kobayashi Y, Baykusheva DR, et al. Probing topological phase transitions
    using high-harmonic generation. <i>Nature Photonics</i>. 2022;16(9):620-624. doi:<a
    href="https://doi.org/10.1038/s41566-022-01050-7">10.1038/s41566-022-01050-7</a>
  apa: Heide, C., Kobayashi, Y., Baykusheva, D. R., Jain, D., Sobota, J. A., Hashimoto,
    M., … Ghimire, S. (2022). Probing topological phase transitions using high-harmonic
    generation. <i>Nature Photonics</i>. Springer Nature. <a href="https://doi.org/10.1038/s41566-022-01050-7">https://doi.org/10.1038/s41566-022-01050-7</a>
  chicago: Heide, Christian, Yuki Kobayashi, Denitsa Rangelova Baykusheva, Deepti
    Jain, Jonathan A. Sobota, Makoto Hashimoto, Patrick S. Kirchmann, et al. “Probing
    Topological Phase Transitions Using High-Harmonic Generation.” <i>Nature Photonics</i>.
    Springer Nature, 2022. <a href="https://doi.org/10.1038/s41566-022-01050-7">https://doi.org/10.1038/s41566-022-01050-7</a>.
  ieee: C. Heide <i>et al.</i>, “Probing topological phase transitions using high-harmonic
    generation,” <i>Nature Photonics</i>, vol. 16, no. 9. Springer Nature, pp. 620–624,
    2022.
  ista: Heide C, Kobayashi Y, Baykusheva DR, Jain D, Sobota JA, Hashimoto M, Kirchmann
    PS, Oh S, Heinz TF, Reis DA, Ghimire S. 2022. Probing topological phase transitions
    using high-harmonic generation. Nature Photonics. 16(9), 620–624.
  mla: Heide, Christian, et al. “Probing Topological Phase Transitions Using High-Harmonic
    Generation.” <i>Nature Photonics</i>, vol. 16, no. 9, Springer Nature, 2022, pp.
    620–24, doi:<a href="https://doi.org/10.1038/s41566-022-01050-7">10.1038/s41566-022-01050-7</a>.
  short: C. Heide, Y. Kobayashi, D.R. Baykusheva, D. Jain, J.A. Sobota, M. Hashimoto,
    P.S. Kirchmann, S. Oh, T.F. Heinz, D.A. Reis, S. Ghimire, Nature Photonics 16
    (2022) 620–624.
date_created: 2023-08-09T13:07:51Z
date_published: 2022-09-01T00:00:00Z
date_updated: 2023-08-22T07:20:09Z
day: '01'
doi: 10.1038/s41566-022-01050-7
extern: '1'
intvolume: '        16'
issue: '9'
keyword:
- Atomic and Molecular Physics
- and Optics
- Electronic
- Optical and Magnetic Materials
language:
- iso: eng
month: '09'
oa_version: None
page: 620-624
publication: Nature Photonics
publication_identifier:
  eissn:
  - 1749-4893
  issn:
  - 1749-4885
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Probing topological phase transitions using high-harmonic generation
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 16
year: '2022'
...
---
_id: '10584'
abstract:
- lang: eng
  text: Electrically tunable lenses (ETLs) are those with the ability to alter their
    optical power in response to an electric signal. This feature allows such systems
    to not only image the areas of interest but also obtain spatial depth perception
    (depth of field, DOF). The aim of the present study was to develop an ETL-based
    imaging system for quantitative surface analysis. Firstly, the system was calibrated
    to achieve high depth resolution, warranting the accurate measurement of the depth
    and to account for and correct any influences from external factors on the ETL.
    This was completed using the Tenengrad operator which effectively identified the
    plane of best focus as demonstrated by the linear relationship between the control
    current applied to the ETL and the height at which the optical system focuses.
    The system was then employed to measure amplitude, spatial, hybrid, and volume
    surface texture parameters of a model material (pharmaceutical dosage form) which
    were validated against the parameters obtained using a previously validated surface
    texture analysis technique, optical profilometry. There were no statistically
    significant differences between the surface texture parameters measured by the
    techniques, highlighting the potential application of ETL-based imaging systems
    as an easily adaptable and low-cost alternative surface texture analysis technique
    to conventional microscopy techniques
acknowledgement: The authors acknowledge the financial assistance provided by the
  University of Huddersfield.
article_number: '17'
article_processing_charge: Yes
article_type: original
author:
- first_name: Jorabar Singh
  full_name: Nirwan, Jorabar Singh
  last_name: Nirwan
- first_name: Shan
  full_name: Lou, Shan
  last_name: Lou
- first_name: Saqib
  full_name: Hussain, Saqib
  last_name: Hussain
- first_name: Muhammad
  full_name: Nauman, Muhammad
  id: 32c21954-2022-11eb-9d5f-af9f93c24e71
  last_name: Nauman
  orcid: 0000-0002-2111-4846
- first_name: Tariq
  full_name: Hussain, Tariq
  last_name: Hussain
- first_name: Barbara R.
  full_name: Conway, Barbara R.
  last_name: Conway
- first_name: Muhammad Usman
  full_name: Ghori, Muhammad Usman
  last_name: Ghori
citation:
  ama: Nirwan JS, Lou S, Hussain S, et al. Electrically tunable lens (ETL) - based
    variable focus imaging system for parametric surface texture analysis of materials.
    <i>Micromachines</i>. 2022;13(1). doi:<a href="https://doi.org/10.3390/mi13010017">10.3390/mi13010017</a>
  apa: Nirwan, J. S., Lou, S., Hussain, S., Nauman, M., Hussain, T., Conway, B. R.,
    &#38; Ghori, M. U. (2022). Electrically tunable lens (ETL) - based variable focus
    imaging system for parametric surface texture analysis of materials. <i>Micromachines</i>.
    MDPI. <a href="https://doi.org/10.3390/mi13010017">https://doi.org/10.3390/mi13010017</a>
  chicago: Nirwan, Jorabar Singh, Shan Lou, Saqib Hussain, Muhammad Nauman, Tariq
    Hussain, Barbara R. Conway, and Muhammad Usman Ghori. “Electrically Tunable Lens
    (ETL) - Based Variable Focus Imaging System for Parametric Surface Texture Analysis
    of Materials.” <i>Micromachines</i>. MDPI, 2022. <a href="https://doi.org/10.3390/mi13010017">https://doi.org/10.3390/mi13010017</a>.
  ieee: J. S. Nirwan <i>et al.</i>, “Electrically tunable lens (ETL) - based variable
    focus imaging system for parametric surface texture analysis of materials,” <i>Micromachines</i>,
    vol. 13, no. 1. MDPI, 2022.
  ista: Nirwan JS, Lou S, Hussain S, Nauman M, Hussain T, Conway BR, Ghori MU. 2022.
    Electrically tunable lens (ETL) - based variable focus imaging system for parametric
    surface texture analysis of materials. Micromachines. 13(1), 17.
  mla: Nirwan, Jorabar Singh, et al. “Electrically Tunable Lens (ETL) - Based Variable
    Focus Imaging System for Parametric Surface Texture Analysis of Materials.” <i>Micromachines</i>,
    vol. 13, no. 1, 17, MDPI, 2022, doi:<a href="https://doi.org/10.3390/mi13010017">10.3390/mi13010017</a>.
  short: J.S. Nirwan, S. Lou, S. Hussain, M. Nauman, T. Hussain, B.R. Conway, M.U.
    Ghori, Micromachines 13 (2022).
date_created: 2022-01-02T23:01:33Z
date_published: 2022-01-01T00:00:00Z
date_updated: 2023-08-09T10:16:10Z
day: '01'
ddc:
- '620'
department:
- _id: KiMo
doi: 10.3390/mi13010017
external_id:
  isi:
  - '000758547200001'
file:
- access_level: open_access
  checksum: 5d062cae3f1acb251cacb21021724c4e
  content_type: application/pdf
  creator: alisjak
  date_created: 2022-01-03T13:43:01Z
  date_updated: 2022-01-03T13:43:01Z
  file_id: '10601'
  file_name: 2021_Micromachines_Singh.pdf
  file_size: 5370675
  relation: main_file
  success: 1
file_date_updated: 2022-01-03T13:43:01Z
has_accepted_license: '1'
intvolume: '        13'
isi: 1
issue: '1'
keyword:
- surface texture
- electrically tunable lens
- materials
- hypromellose
- surface topography
- surface roughness
- pharmaceutical tablet
- variable focus imaging
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
publication: Micromachines
publication_identifier:
  eissn:
  - 2072-666X
publication_status: published
publisher: MDPI
quality_controlled: '1'
scopus_import: '1'
status: public
title: Electrically tunable lens (ETL) - based variable focus imaging system for parametric
  surface texture analysis of materials
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 13
year: '2022'
...
---
_id: '10589'
abstract:
- lang: eng
  text: Superconducting devices ubiquitously have an excess of broken Cooper pairs,
    which can hamper their performance. It is widely believed that external radiation
    is responsible but a study now suggests there must be an additional, unknown source.
article_processing_charge: No
article_type: letter_note
author:
- first_name: Andrew P
  full_name: Higginbotham, Andrew P
  id: 4AD6785A-F248-11E8-B48F-1D18A9856A87
  last_name: Higginbotham
  orcid: 0000-0003-2607-2363
citation:
  ama: Higginbotham AP. A secret source. <i>Nature Physics</i>. 2022;18:126. doi:<a
    href="https://doi.org/10.1038/s41567-021-01459-x">10.1038/s41567-021-01459-x</a>
  apa: Higginbotham, A. P. (2022). A secret source. <i>Nature Physics</i>. Springer
    Nature. <a href="https://doi.org/10.1038/s41567-021-01459-x">https://doi.org/10.1038/s41567-021-01459-x</a>
  chicago: Higginbotham, Andrew P. “A Secret Source.” <i>Nature Physics</i>. Springer
    Nature, 2022. <a href="https://doi.org/10.1038/s41567-021-01459-x">https://doi.org/10.1038/s41567-021-01459-x</a>.
  ieee: A. P. Higginbotham, “A secret source,” <i>Nature Physics</i>, vol. 18. Springer
    Nature, p. 126, 2022.
  ista: Higginbotham AP. 2022. A secret source. Nature Physics. 18, 126.
  mla: Higginbotham, Andrew P. “A Secret Source.” <i>Nature Physics</i>, vol. 18,
    Springer Nature, 2022, p. 126, doi:<a href="https://doi.org/10.1038/s41567-021-01459-x">10.1038/s41567-021-01459-x</a>.
  short: A.P. Higginbotham, Nature Physics 18 (2022) 126.
date_created: 2022-01-02T23:01:35Z
date_published: 2022-02-01T00:00:00Z
date_updated: 2023-08-02T13:43:11Z
day: '01'
department:
- _id: AnHi
doi: 10.1038/s41567-021-01459-x
external_id:
  isi:
  - '000733431000007'
intvolume: '        18'
isi: 1
keyword:
- superconducting devices
- superconducting properties and materials
language:
- iso: eng
month: '02'
oa_version: None
page: '126'
publication: Nature Physics
publication_identifier:
  eissn:
  - 1745-2481
  issn:
  - 1745-2473
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: A secret source
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 18
year: '2022'
...
---
_id: '12137'
abstract:
- lang: eng
  text: We investigate the local self-sustained process underlying spiral turbulence
    in counter-rotating Taylor–Couette flow using a periodic annular domain, shaped
    as a parallelogram, two of whose sides are aligned with the cylindrical helix
    described by the spiral pattern. The primary focus of the study is placed on the
    emergence of drifting–rotating waves (DRW) that capture, in a relatively small
    domain, the main features of coherent structures typically observed in developed
    turbulence. The transitional dynamics of the subcritical region, far below the
    first instability of the laminar circular Couette flow, is determined by the upper
    and lower branches of DRW solutions originated at saddle-node bifurcations. The
    mechanism whereby these solutions self-sustain, and the chaotic dynamics they
    induce, are conspicuously reminiscent of other subcritical shear flows. Remarkably,
    the flow properties of DRW persist even as the Reynolds number is increased beyond
    the linear stability threshold of the base flow. Simulations in a narrow parallelogram
    domain stretched in the azimuthal direction to revolve around the apparatus a
    full turn confirm that self-sustained vortices eventually concentrate into a localised
    pattern. The resulting statistical steady state satisfactorily reproduces qualitatively,
    and to a certain degree also quantitatively, the topology and properties of spiral
    turbulence as calculated in a large periodic domain of sufficient aspect ratio
    that is representative of the real system.
acknowledgement: "K.D.’s research was supported by an Australian Research Council
  Discovery Early Career\r\nResearcher Award (DE170100171). B.W., R.A., F.M. and A.M.
  research was supported by the Spanish Ministerio de Economía y Competitivdad (grant
  numbers FIS2016-77849-R and FIS2017-85794-P) and Ministerio de Ciencia e Innovación
  (grant number PID2020-114043GB-I00) and the Generalitat de Catalunya (grant 2017-SGR-785).
  B.W.’s research was also supported by the Chinese Scholarship Council (grant CSC
  no. 201806440152)."
article_number: A21
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: B.
  full_name: Wang, B.
  last_name: Wang
- first_name: Roger
  full_name: Ayats López, Roger
  id: ab77522d-073b-11ed-8aff-e71b39258362
  last_name: Ayats López
  orcid: 0000-0001-6572-0621
- first_name: K.
  full_name: Deguchi, K.
  last_name: Deguchi
- first_name: F.
  full_name: Mellibovsky, F.
  last_name: Mellibovsky
- first_name: A.
  full_name: Meseguer, A.
  last_name: Meseguer
citation:
  ama: Wang B, Ayats López R, Deguchi K, Mellibovsky F, Meseguer A. Self-sustainment
    of coherent structures in counter-rotating Taylor–Couette flow. <i>Journal of
    Fluid Mechanics</i>. 2022;951. doi:<a href="https://doi.org/10.1017/jfm.2022.828">10.1017/jfm.2022.828</a>
  apa: Wang, B., Ayats López, R., Deguchi, K., Mellibovsky, F., &#38; Meseguer, A.
    (2022). Self-sustainment of coherent structures in counter-rotating Taylor–Couette
    flow. <i>Journal of Fluid Mechanics</i>. Cambridge University Press. <a href="https://doi.org/10.1017/jfm.2022.828">https://doi.org/10.1017/jfm.2022.828</a>
  chicago: Wang, B., Roger Ayats López, K. Deguchi, F. Mellibovsky, and A. Meseguer.
    “Self-Sustainment of Coherent Structures in Counter-Rotating Taylor–Couette Flow.”
    <i>Journal of Fluid Mechanics</i>. Cambridge University Press, 2022. <a href="https://doi.org/10.1017/jfm.2022.828">https://doi.org/10.1017/jfm.2022.828</a>.
  ieee: B. Wang, R. Ayats López, K. Deguchi, F. Mellibovsky, and A. Meseguer, “Self-sustainment
    of coherent structures in counter-rotating Taylor–Couette flow,” <i>Journal of
    Fluid Mechanics</i>, vol. 951. Cambridge University Press, 2022.
  ista: Wang B, Ayats López R, Deguchi K, Mellibovsky F, Meseguer A. 2022. Self-sustainment
    of coherent structures in counter-rotating Taylor–Couette flow. Journal of Fluid
    Mechanics. 951, A21.
  mla: Wang, B., et al. “Self-Sustainment of Coherent Structures in Counter-Rotating
    Taylor–Couette Flow.” <i>Journal of Fluid Mechanics</i>, vol. 951, A21, Cambridge
    University Press, 2022, doi:<a href="https://doi.org/10.1017/jfm.2022.828">10.1017/jfm.2022.828</a>.
  short: B. Wang, R. Ayats López, K. Deguchi, F. Mellibovsky, A. Meseguer, Journal
    of Fluid Mechanics 951 (2022).
date_created: 2023-01-12T12:04:17Z
date_published: 2022-11-07T00:00:00Z
date_updated: 2023-08-04T08:54:16Z
day: '07'
department:
- _id: BjHo
doi: 10.1017/jfm.2022.828
external_id:
  arxiv:
  - '2207.12990'
  isi:
  - '000879446900001'
intvolume: '       951'
isi: 1
keyword:
- Mechanical Engineering
- Mechanics of Materials
- Condensed Matter Physics
- Applied Mathematics
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: ' https://doi.org/10.48550/arXiv.2207.12990'
month: '11'
oa: 1
oa_version: Preprint
publication: Journal of Fluid Mechanics
publication_identifier:
  eissn:
  - 1469-7645
  issn:
  - 0022-1120
publication_status: published
publisher: Cambridge University Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: Self-sustainment of coherent structures in counter-rotating Taylor–Couette
  flow
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 951
year: '2022'
...
---
_id: '12146'
abstract:
- lang: eng
  text: 'In this paper, we explore the stability and dynamical relevance of a wide
    variety of steady, time-periodic, quasiperiodic, and chaotic flows arising between
    orthogonally stretching parallel plates. We first explore the stability of all
    the steady flow solution families formerly identified by Ayats et al. [“Flows
    between orthogonally stretching parallel plates,” Phys. Fluids 33, 024103 (2021)],
    concluding that only the one that originates from the Stokesian approximation
    is actually stable. When both plates are shrinking at identical or nearly the
    same deceleration rates, this Stokesian flow exhibits a Hopf bifurcation that
    leads to stable time-periodic regimes. The resulting time-periodic orbits or flows
    are tracked for different Reynolds numbers and stretching rates while monitoring
    their Floquet exponents to identify secondary instabilities. It is found that
    these time-periodic flows also exhibit Neimark–Sacker bifurcations, generating
    stable quasiperiodic flows (tori) that may sometimes give rise to chaotic dynamics
    through a Ruelle–Takens–Newhouse scenario. However, chaotic dynamics is unusually
    observed, as the quasiperiodic flows generally become phase-locked through a resonance
    mechanism before a strange attractor may arise, thus restoring the time-periodicity
    of the flow. In this work, we have identified and tracked four different resonance
    regions, also known as Arnold tongues or horns. In particular, the 1 : 4 strong
    resonance region is explored in great detail, where the identified scenarios are
    in very good agreement with normal form theory. '
acknowledgement: "This work was supported by the Spanish MINECO under Grant Nos. FIS2017-85794-P
  and PRX18/00179, the Spanish MICINN through Grant No. PID2020-114043GB-I00, and
  the\r\nGeneralitat de Catalunya under Grant No. 2017-SGR-785. B.W.’s research was
  also supported by the Chinese Scholarship Council through Grant CSC No. 201806440152."
article_number: '114111'
article_processing_charge: No
article_type: original
author:
- first_name: B.
  full_name: Wang, B.
  last_name: Wang
- first_name: Roger
  full_name: Ayats López, Roger
  id: ab77522d-073b-11ed-8aff-e71b39258362
  last_name: Ayats López
  orcid: 0000-0001-6572-0621
- first_name: A.
  full_name: Meseguer, A.
  last_name: Meseguer
- first_name: F.
  full_name: Marques, F.
  last_name: Marques
citation:
  ama: Wang B, Ayats López R, Meseguer A, Marques F. Phase-locking flows between orthogonally
    stretching parallel plates. <i>Physics of Fluids</i>. 2022;34(11). doi:<a href="https://doi.org/10.1063/5.0124152">10.1063/5.0124152</a>
  apa: Wang, B., Ayats López, R., Meseguer, A., &#38; Marques, F. (2022). Phase-locking
    flows between orthogonally stretching parallel plates. <i>Physics of Fluids</i>.
    AIP Publishing. <a href="https://doi.org/10.1063/5.0124152">https://doi.org/10.1063/5.0124152</a>
  chicago: Wang, B., Roger Ayats López, A. Meseguer, and F. Marques. “Phase-Locking
    Flows between Orthogonally Stretching Parallel Plates.” <i>Physics of Fluids</i>.
    AIP Publishing, 2022. <a href="https://doi.org/10.1063/5.0124152">https://doi.org/10.1063/5.0124152</a>.
  ieee: B. Wang, R. Ayats López, A. Meseguer, and F. Marques, “Phase-locking flows
    between orthogonally stretching parallel plates,” <i>Physics of Fluids</i>, vol.
    34, no. 11. AIP Publishing, 2022.
  ista: Wang B, Ayats López R, Meseguer A, Marques F. 2022. Phase-locking flows between
    orthogonally stretching parallel plates. Physics of Fluids. 34(11), 114111.
  mla: Wang, B., et al. “Phase-Locking Flows between Orthogonally Stretching Parallel
    Plates.” <i>Physics of Fluids</i>, vol. 34, no. 11, 114111, AIP Publishing, 2022,
    doi:<a href="https://doi.org/10.1063/5.0124152">10.1063/5.0124152</a>.
  short: B. Wang, R. Ayats López, A. Meseguer, F. Marques, Physics of Fluids 34 (2022).
date_created: 2023-01-12T12:06:58Z
date_published: 2022-11-04T00:00:00Z
date_updated: 2023-10-03T11:07:58Z
day: '04'
department:
- _id: BjHo
doi: 10.1063/5.0124152
external_id:
  isi:
  - '000880665300024'
intvolume: '        34'
isi: 1
issue: '11'
keyword:
- Condensed Matter Physics
- Fluid Flow and Transfer Processes
- Mechanics of Materials
- Computational Mechanics
- Mechanical Engineering
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://upcommons.upc.edu/handle/2117/385635
month: '11'
oa: 1
oa_version: Submitted Version
publication: Physics of Fluids
publication_identifier:
  eissn:
  - 1089-7666
  issn:
  - 1070-6631
publication_status: published
publisher: AIP Publishing
quality_controlled: '1'
scopus_import: '1'
status: public
title: Phase-locking flows between orthogonally stretching parallel plates
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 34
year: '2022'
...
---
_id: '9235'
abstract:
- lang: eng
  text: Cu2–xS has become one of the most promising thermoelectric materials for application
    in the middle-high temperature range. Its advantages include the abundance, low
    cost, and safety of its elements and a high performance at relatively elevated
    temperatures. However, stability issues limit its operation current and temperature,
    thus calling for the optimization of the material performance in the middle temperature
    range. Here, we present a synthetic protocol for large scale production of covellite
    CuS nanoparticles at ambient temperature and atmosphere, and using water as a
    solvent. The crystal phase and stoichiometry of the particles are afterward tuned
    through an annealing process at a moderate temperature under inert or reducing
    atmosphere. While annealing under argon results in Cu1.8S nanopowder with a rhombohedral
    crystal phase, annealing in an atmosphere containing hydrogen leads to tetragonal
    Cu1.96S. High temperature X-ray diffraction analysis shows the material annealed
    in argon to transform to the cubic phase at ca. 400 K, while the material annealed
    in the presence of hydrogen undergoes two phase transitions, first to hexagonal
    and then to the cubic structure. The annealing atmosphere, temperature, and time
    allow adjustment of the density of copper vacancies and thus tuning of the charge
    carrier concentration and material transport properties. In this direction, the
    material annealed under Ar is characterized by higher electrical conductivities
    but lower Seebeck coefficients than the material annealed in the presence of hydrogen.
    By optimizing the charge carrier concentration through the annealing time, Cu2–xS
    with record figures of merit in the middle temperature range, up to 1.41 at 710
    K, is obtained. We finally demonstrate that this strategy, based on a low-cost
    and scalable solution synthesis process, is also suitable for the production of
    high performance Cu2–xS layers using high throughput and cost-effective printing
    technologies.
acknowledgement: This work was supported by the European Regional Development Funds.
  M.Y.L., X.H., T.Z., and K.X. thank the China Scholarship Council for scholarship
  support. M.I. acknowledges financial support from IST Austria. J.L. acknowledges
  support from the National Natural Science Foundation of China (No. 22008091), the
  funding for scientific research startup of Jiangsu University (No. 19JDG044), and
  Jiangsu Provincial Program for High-Level Innovative and Entrepreneurial Talents
  Introduction. J.L. is a Serra Húnter fellow and is grateful to the ICREA Academia
  program and projects MICINN/FEDER RTI2018-093996-B-C31 and GC 2017 SGR 128. ICN2
  acknowledges funding from Generalitat de Catalunya 2017 SGR 327 and the Spanish
  MINECO ENE2017-85087-C3. ICN2 is supported by the Severo Ochoa program from Spanish
  MINECO (Grant No. SEV-2017-0706) and is funded by the CERCA Programme/Generalitat
  de Catalunya. Part of the present work has been performed in the framework of Universitat
  Autònoma de Barcelona Materials Science PhD program. T.Z. has received funding from
  the CSC-UAB PhD scholarship program.
article_processing_charge: No
article_type: original
author:
- first_name: Mengyao
  full_name: Li, Mengyao
  last_name: Li
- first_name: Yu
  full_name: Liu, Yu
  id: 2A70014E-F248-11E8-B48F-1D18A9856A87
  last_name: Liu
  orcid: 0000-0001-7313-6740
- first_name: Yu
  full_name: Zhang, Yu
  last_name: Zhang
- first_name: Xu
  full_name: Han, Xu
  last_name: Han
- first_name: Ting
  full_name: Zhang, Ting
  last_name: Zhang
- first_name: Yong
  full_name: Zuo, Yong
  last_name: Zuo
- first_name: Chenyang
  full_name: Xie, Chenyang
  last_name: Xie
- first_name: Ke
  full_name: Xiao, Ke
  last_name: Xiao
- first_name: Jordi
  full_name: Arbiol, Jordi
  last_name: Arbiol
- first_name: Jordi
  full_name: Llorca, Jordi
  last_name: Llorca
- first_name: Maria
  full_name: Ibáñez, Maria
  id: 43C61214-F248-11E8-B48F-1D18A9856A87
  last_name: Ibáñez
  orcid: 0000-0001-5013-2843
- first_name: Junfeng
  full_name: Liu, Junfeng
  last_name: Liu
- first_name: Andreu
  full_name: Cabot, Andreu
  last_name: Cabot
citation:
  ama: Li M, Liu Y, Zhang Y, et al. Effect of the annealing atmosphere on crystal
    phase and thermoelectric properties of copper sulfide. <i>ACS Nano</i>. 2021;15(3):4967–4978.
    doi:<a href="https://doi.org/10.1021/acsnano.0c09866">10.1021/acsnano.0c09866</a>
  apa: Li, M., Liu, Y., Zhang, Y., Han, X., Zhang, T., Zuo, Y., … Cabot, A. (2021).
    Effect of the annealing atmosphere on crystal phase and thermoelectric properties
    of copper sulfide. <i>ACS Nano</i>. American Chemical Society . <a href="https://doi.org/10.1021/acsnano.0c09866">https://doi.org/10.1021/acsnano.0c09866</a>
  chicago: Li, Mengyao, Yu Liu, Yu Zhang, Xu Han, Ting Zhang, Yong Zuo, Chenyang Xie,
    et al. “Effect of the Annealing Atmosphere on Crystal Phase and Thermoelectric
    Properties of Copper Sulfide.” <i>ACS Nano</i>. American Chemical Society , 2021.
    <a href="https://doi.org/10.1021/acsnano.0c09866">https://doi.org/10.1021/acsnano.0c09866</a>.
  ieee: M. Li <i>et al.</i>, “Effect of the annealing atmosphere on crystal phase
    and thermoelectric properties of copper sulfide,” <i>ACS Nano</i>, vol. 15, no.
    3. American Chemical Society , pp. 4967–4978, 2021.
  ista: Li M, Liu Y, Zhang Y, Han X, Zhang T, Zuo Y, Xie C, Xiao K, Arbiol J, Llorca
    J, Ibáñez M, Liu J, Cabot A. 2021. Effect of the annealing atmosphere on crystal
    phase and thermoelectric properties of copper sulfide. ACS Nano. 15(3), 4967–4978.
  mla: Li, Mengyao, et al. “Effect of the Annealing Atmosphere on Crystal Phase and
    Thermoelectric Properties of Copper Sulfide.” <i>ACS Nano</i>, vol. 15, no. 3,
    American Chemical Society , 2021, pp. 4967–4978, doi:<a href="https://doi.org/10.1021/acsnano.0c09866">10.1021/acsnano.0c09866</a>.
  short: M. Li, Y. Liu, Y. Zhang, X. Han, T. Zhang, Y. Zuo, C. Xie, K. Xiao, J. Arbiol,
    J. Llorca, M. Ibáñez, J. Liu, A. Cabot, ACS Nano 15 (2021) 4967–4978.
date_created: 2021-03-10T20:12:45Z
date_published: 2021-03-01T00:00:00Z
date_updated: 2023-10-03T09:59:55Z
day: '01'
department:
- _id: MaIb
doi: 10.1021/acsnano.0c09866
external_id:
  isi:
  - '000634569100106'
  pmid:
  - '33645986'
intvolume: '        15'
isi: 1
issue: '3'
keyword:
- General Engineering
- General Physics and Astronomy
- General Materials Science
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://upcommons.upc.edu/bitstream/handle/2117/363528/Pb%20mengyao.pdf?sequence=1&isAllowed=y
month: '03'
oa: 1
oa_version: Submitted Version
page: 4967–4978
pmid: 1
publication: ACS Nano
publication_identifier:
  eissn:
  - 1936-086X
  issn:
  - 1936-0851
publication_status: published
publisher: 'American Chemical Society '
quality_controlled: '1'
scopus_import: '1'
status: public
title: Effect of the annealing atmosphere on crystal phase and thermoelectric properties
  of copper sulfide
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 15
year: '2021'
...
---
_id: '9282'
abstract:
- lang: eng
  text: Several Ising-type magnetic van der Waals (vdW) materials exhibit stable magnetic
    ground states. Despite these clear experimental demonstrations, a complete theoretical
    and microscopic understanding of their magnetic anisotropy is still lacking. In
    particular, the validity limit of identifying their one-dimensional (1-D) Ising
    nature has remained uninvestigated in a quantitative way. Here we performed the
    complete mapping of magnetic anisotropy for a prototypical Ising vdW magnet FePS3
    for the first time. Combining torque magnetometry measurements with their magnetostatic
    model analysis and the relativistic density functional total energy calculations,
    we successfully constructed the three-dimensional (3-D) mappings of the magnetic
    anisotropy in terms of magnetic torque and energy. The results not only quantitatively
    confirm that the easy axis is perpendicular to the ab plane, but also reveal the
    anisotropies within the ab, ac, and bc planes. Our approach can be applied to
    the detailed quantitative study of magnetism in vdW materials.
article_number: '035011'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Muhammad
  full_name: Nauman, Muhammad
  id: 32c21954-2022-11eb-9d5f-af9f93c24e71
  last_name: Nauman
  orcid: 0000-0002-2111-4846
- first_name: Do Hoon
  full_name: Kiem, Do Hoon
  last_name: Kiem
- first_name: Sungmin
  full_name: Lee, Sungmin
  last_name: Lee
- first_name: Suhan
  full_name: Son, Suhan
  last_name: Son
- first_name: J-G
  full_name: Park, J-G
  last_name: Park
- first_name: Woun
  full_name: Kang, Woun
  last_name: Kang
- first_name: Myung Joon
  full_name: Han, Myung Joon
  last_name: Han
- first_name: Youn Jung
  full_name: Jo, Youn Jung
  last_name: Jo
citation:
  ama: Nauman M, Kiem DH, Lee S, et al. Complete mapping of magnetic anisotropy for
    prototype Ising van der Waals FePS3. <i>2D Materials</i>. 2021;8(3). doi:<a href="https://doi.org/10.1088/2053-1583/abeed3">10.1088/2053-1583/abeed3</a>
  apa: Nauman, M., Kiem, D. H., Lee, S., Son, S., Park, J.-G., Kang, W., … Jo, Y.
    J. (2021). Complete mapping of magnetic anisotropy for prototype Ising van der
    Waals FePS3. <i>2D Materials</i>. IOP Publishing. <a href="https://doi.org/10.1088/2053-1583/abeed3">https://doi.org/10.1088/2053-1583/abeed3</a>
  chicago: Nauman, Muhammad, Do Hoon Kiem, Sungmin Lee, Suhan Son, J-G Park, Woun
    Kang, Myung Joon Han, and Youn Jung Jo. “Complete Mapping of Magnetic Anisotropy
    for Prototype Ising van Der Waals FePS3.” <i>2D Materials</i>. IOP Publishing,
    2021. <a href="https://doi.org/10.1088/2053-1583/abeed3">https://doi.org/10.1088/2053-1583/abeed3</a>.
  ieee: M. Nauman <i>et al.</i>, “Complete mapping of magnetic anisotropy for prototype
    Ising van der Waals FePS3,” <i>2D Materials</i>, vol. 8, no. 3. IOP Publishing,
    2021.
  ista: Nauman M, Kiem DH, Lee S, Son S, Park J-G, Kang W, Han MJ, Jo YJ. 2021. Complete
    mapping of magnetic anisotropy for prototype Ising van der Waals FePS3. 2D Materials.
    8(3), 035011.
  mla: Nauman, Muhammad, et al. “Complete Mapping of Magnetic Anisotropy for Prototype
    Ising van Der Waals FePS3.” <i>2D Materials</i>, vol. 8, no. 3, 035011, IOP Publishing,
    2021, doi:<a href="https://doi.org/10.1088/2053-1583/abeed3">10.1088/2053-1583/abeed3</a>.
  short: M. Nauman, D.H. Kiem, S. Lee, S. Son, J.-G. Park, W. Kang, M.J. Han, Y.J.
    Jo, 2D Materials 8 (2021).
date_created: 2021-03-23T07:10:17Z
date_published: 2021-04-06T00:00:00Z
date_updated: 2021-12-01T10:36:56Z
day: '06'
department:
- _id: KiMo
doi: 10.1088/2053-1583/abeed3
extern: '1'
external_id:
  arxiv:
  - '2103.09029'
intvolume: '         8'
issue: '3'
keyword:
- Mechanical Engineering
- General Materials Science
- Mechanics of Materials
- General Chemistry
- Condensed Matter Physics
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/2103.09029
month: '04'
oa: 1
oa_version: Preprint
publication: 2D Materials
publication_identifier:
  issn:
  - 2053-1583
publication_status: published
publisher: IOP Publishing
quality_controlled: '1'
status: public
title: Complete mapping of magnetic anisotropy for prototype Ising van der Waals FePS3
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 8
year: '2021'
...
---
_id: '13359'
abstract:
- lang: eng
  text: Dissipative self-assembly is ubiquitous in nature, where it gives rise to
    complex structures and functions such as self-healing, homeostasis, and camouflage.
    These phenomena are enabled by the continuous conversion of energy stored in chemical
    fuels, such as ATP. Over the past decade, an increasing number of synthetic chemically
    driven systems have been reported that mimic the features of their natural counterparts.
    At the same time, it has been shown that dissipative self-assembly can also be
    fueled by light; these optically fueled systems have been developed in parallel
    to the chemically fueled ones. In this perspective, we critically compare these
    two classes of systems. Despite the complementarity and fundamental differences
    between these two modes of dissipative self-assembly, our analysis reveals that
    multiple analogies exist between chemically and light-fueled systems. We hope
    that these considerations will facilitate further development of the field of
    dissipative self-assembly.
article_processing_charge: No
article_type: original
author:
- first_name: Maren
  full_name: Weißenfels, Maren
  last_name: Weißenfels
- first_name: Julius
  full_name: Gemen, Julius
  last_name: Gemen
- first_name: Rafal
  full_name: Klajn, Rafal
  id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b
  last_name: Klajn
citation:
  ama: 'Weißenfels M, Gemen J, Klajn R. Dissipative self-assembly: Fueling with chemicals
    versus light. <i>Chem</i>. 2021;7(1):23-37. doi:<a href="https://doi.org/10.1016/j.chempr.2020.11.025">10.1016/j.chempr.2020.11.025</a>'
  apa: 'Weißenfels, M., Gemen, J., &#38; Klajn, R. (2021). Dissipative self-assembly:
    Fueling with chemicals versus light. <i>Chem</i>. Elsevier. <a href="https://doi.org/10.1016/j.chempr.2020.11.025">https://doi.org/10.1016/j.chempr.2020.11.025</a>'
  chicago: 'Weißenfels, Maren, Julius Gemen, and Rafal Klajn. “Dissipative Self-Assembly:
    Fueling with Chemicals versus Light.” <i>Chem</i>. Elsevier, 2021. <a href="https://doi.org/10.1016/j.chempr.2020.11.025">https://doi.org/10.1016/j.chempr.2020.11.025</a>.'
  ieee: 'M. Weißenfels, J. Gemen, and R. Klajn, “Dissipative self-assembly: Fueling
    with chemicals versus light,” <i>Chem</i>, vol. 7, no. 1. Elsevier, pp. 23–37,
    2021.'
  ista: 'Weißenfels M, Gemen J, Klajn R. 2021. Dissipative self-assembly: Fueling
    with chemicals versus light. Chem. 7(1), 23–37.'
  mla: 'Weißenfels, Maren, et al. “Dissipative Self-Assembly: Fueling with Chemicals
    versus Light.” <i>Chem</i>, vol. 7, no. 1, Elsevier, 2021, pp. 23–37, doi:<a href="https://doi.org/10.1016/j.chempr.2020.11.025">10.1016/j.chempr.2020.11.025</a>.'
  short: M. Weißenfels, J. Gemen, R. Klajn, Chem 7 (2021) 23–37.
date_created: 2023-08-01T09:35:19Z
date_published: 2021-01-14T00:00:00Z
date_updated: 2023-08-07T10:04:28Z
day: '14'
doi: 10.1016/j.chempr.2020.11.025
extern: '1'
intvolume: '         7'
issue: '1'
keyword:
- Materials Chemistry
- Biochemistry (medical)
- General Chemical Engineering
- Environmental Chemistry
- Biochemistry
- General Chemistry
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1016/j.chempr.2020.11.025
month: '01'
oa: 1
oa_version: Published Version
page: 23-37
publication: Chem
publication_identifier:
  issn:
  - 2451-9294
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Dissipative self-assembly: Fueling with chemicals versus light'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 7
year: '2021'
...
---
_id: '13996'
abstract:
- lang: eng
  text: We report the observation of an anomalous nonlinear optical response of the
    prototypical three-dimensional topological insulator bismuth selenide through
    the process of high-order harmonic generation. We find that the generation efficiency
    increases as the laser polarization is changed from linear to elliptical, and
    it becomes maximum for circular polarization. With the aid of a microscopic theory
    and a detailed analysis of the measured spectra, we reveal that such anomalous
    enhancement encodes the characteristic topology of the band structure that originates
    from the interplay of strong spin–orbit coupling and time-reversal symmetry protection.
    The implications are in ultrafast probing of topological phase transitions, light-field
    driven dissipationless electronics, and quantum computation.
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Denitsa Rangelova
  full_name: Baykusheva, Denitsa Rangelova
  id: 71b4d059-2a03-11ee-914d-dfa3beed6530
  last_name: Baykusheva
- first_name: Alexis
  full_name: Chacón, Alexis
  last_name: Chacón
- first_name: Jian
  full_name: Lu, Jian
  last_name: Lu
- first_name: Trevor P.
  full_name: Bailey, Trevor P.
  last_name: Bailey
- first_name: Jonathan A.
  full_name: Sobota, Jonathan A.
  last_name: Sobota
- first_name: Hadas
  full_name: Soifer, Hadas
  last_name: Soifer
- first_name: Patrick S.
  full_name: Kirchmann, Patrick S.
  last_name: Kirchmann
- first_name: Costel
  full_name: Rotundu, Costel
  last_name: Rotundu
- first_name: Ctirad
  full_name: Uher, Ctirad
  last_name: Uher
- first_name: Tony F.
  full_name: Heinz, Tony F.
  last_name: Heinz
- first_name: David A.
  full_name: Reis, David A.
  last_name: Reis
- first_name: Shambhu
  full_name: Ghimire, Shambhu
  last_name: Ghimire
citation:
  ama: Baykusheva DR, Chacón A, Lu J, et al. All-optical probe of three-dimensional
    topological insulators based on high-harmonic generation by circularly polarized
    laser fields. <i>Nano Letters</i>. 2021;21(21):8970-8978. doi:<a href="https://doi.org/10.1021/acs.nanolett.1c02145">10.1021/acs.nanolett.1c02145</a>
  apa: Baykusheva, D. R., Chacón, A., Lu, J., Bailey, T. P., Sobota, J. A., Soifer,
    H., … Ghimire, S. (2021). All-optical probe of three-dimensional topological insulators
    based on high-harmonic generation by circularly polarized laser fields. <i>Nano
    Letters</i>. American Chemical Society. <a href="https://doi.org/10.1021/acs.nanolett.1c02145">https://doi.org/10.1021/acs.nanolett.1c02145</a>
  chicago: Baykusheva, Denitsa Rangelova, Alexis Chacón, Jian Lu, Trevor P. Bailey,
    Jonathan A. Sobota, Hadas Soifer, Patrick S. Kirchmann, et al. “All-Optical Probe
    of Three-Dimensional Topological Insulators Based on High-Harmonic Generation
    by Circularly Polarized Laser Fields.” <i>Nano Letters</i>. American Chemical
    Society, 2021. <a href="https://doi.org/10.1021/acs.nanolett.1c02145">https://doi.org/10.1021/acs.nanolett.1c02145</a>.
  ieee: D. R. Baykusheva <i>et al.</i>, “All-optical probe of three-dimensional topological
    insulators based on high-harmonic generation by circularly polarized laser fields,”
    <i>Nano Letters</i>, vol. 21, no. 21. American Chemical Society, pp. 8970–8978,
    2021.
  ista: Baykusheva DR, Chacón A, Lu J, Bailey TP, Sobota JA, Soifer H, Kirchmann PS,
    Rotundu C, Uher C, Heinz TF, Reis DA, Ghimire S. 2021. All-optical probe of three-dimensional
    topological insulators based on high-harmonic generation by circularly polarized
    laser fields. Nano Letters. 21(21), 8970–8978.
  mla: Baykusheva, Denitsa Rangelova, et al. “All-Optical Probe of Three-Dimensional
    Topological Insulators Based on High-Harmonic Generation by Circularly Polarized
    Laser Fields.” <i>Nano Letters</i>, vol. 21, no. 21, American Chemical Society,
    2021, pp. 8970–78, doi:<a href="https://doi.org/10.1021/acs.nanolett.1c02145">10.1021/acs.nanolett.1c02145</a>.
  short: D.R. Baykusheva, A. Chacón, J. Lu, T.P. Bailey, J.A. Sobota, H. Soifer, P.S.
    Kirchmann, C. Rotundu, C. Uher, T.F. Heinz, D.A. Reis, S. Ghimire, Nano Letters
    21 (2021) 8970–8978.
date_created: 2023-08-09T13:09:15Z
date_published: 2021-10-22T00:00:00Z
date_updated: 2023-08-22T07:32:00Z
day: '22'
doi: 10.1021/acs.nanolett.1c02145
extern: '1'
external_id:
  arxiv:
  - '2109.15291'
  pmid:
  - '34676752'
intvolume: '        21'
issue: '21'
keyword:
- Mechanical Engineering
- Condensed Matter Physics
- General Materials Science
- General Chemistry
- Bioengineering
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1021/acs.nanolett.1c02145
month: '10'
oa: 1
oa_version: Published Version
page: 8970-8978
pmid: 1
publication: Nano Letters
publication_identifier:
  eissn:
  - 1530-6992
  issn:
  - 1530-6984
publication_status: published
publisher: American Chemical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: All-optical probe of three-dimensional topological insulators based on high-harmonic
  generation by circularly polarized laser fields
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 21
year: '2021'
...
---
_id: '10123'
abstract:
- lang: eng
  text: Solution synthesis of particles emerged as an alternative to prepare thermoelectric
    materials with less demanding processing conditions than conventional solid-state
    synthetic methods. However, solution synthesis generally involves the presence
    of additional molecules or ions belonging to the precursors or added to enable
    solubility and/or regulate nucleation and growth. These molecules or ions can
    end up in the particles as surface adsorbates and interfere in the material properties.
    This work demonstrates that ionic adsorbates, in particular Na⁺ ions, are electrostatically
    adsorbed in SnSe particles synthesized in water and play a crucial role not only
    in directing the material nano/microstructure but also in determining the transport
    properties of the consolidated material. In dense pellets prepared by sintering
    SnSe particles, Na remains within the crystal lattice as dopant, in dislocations,
    precipitates, and forming grain boundary complexions. These results highlight
    the importance of considering all the possible unintentional impurities to establish
    proper structure-property relationships and control material properties in solution-processed
    thermoelectric materials.
acknowledged_ssus:
- _id: EM-Fac
- _id: NanoFab
acknowledgement: 'Y.L. and M.C. contributed equally to this work. This research was
  supported by the Scientific Service Units (SSU) of IST Austria through resources
  provided by Electron Microscopy Facility (EMF) and the Nanofabrication Facility
  (NNF). This work was financially supported by IST Austria and the Werner Siemens
  Foundation. Y.L. acknowledges funding from the European Union''s Horizon 2020 research
  and innovation program under the Marie Sklodowska-Curie grant agreement No. 754411.
  M.C. has received funding from the European Union''s Horizon 2020 research and innovation
  program under the Marie Skłodowska-Curie Grant Agreement No. 665385. Y.Y. and O.C.-M.
  acknowledge the financial support from DFG within the project SFB 917: Nanoswitches.
  J.L. is a Serra Húnter Fellow and is grateful to ICREA Academia program. C.C. acknowledges
  funding from the FWF “Lise Meitner Fellowship” grant agreement M 2889-N.'
article_number: '2106858'
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Yu
  full_name: Liu, Yu
  id: 2A70014E-F248-11E8-B48F-1D18A9856A87
  last_name: Liu
  orcid: 0000-0001-7313-6740
- first_name: Mariano
  full_name: Calcabrini, Mariano
  id: 45D7531A-F248-11E8-B48F-1D18A9856A87
  last_name: Calcabrini
  orcid: 0000-0003-4566-5877
- first_name: Yuan
  full_name: Yu, Yuan
  last_name: Yu
- first_name: Aziz
  full_name: Genç, Aziz
  last_name: Genç
- first_name: Cheng
  full_name: Chang, Cheng
  id: 9E331C2E-9F27-11E9-AE48-5033E6697425
  last_name: Chang
  orcid: 0000-0002-9515-4277
- first_name: Tommaso
  full_name: Costanzo, Tommaso
  id: D93824F4-D9BA-11E9-BB12-F207E6697425
  last_name: Costanzo
  orcid: 0000-0001-9732-3815
- first_name: Tobias
  full_name: Kleinhanns, Tobias
  id: 8BD9DE16-AB3C-11E9-9C8C-2A03E6697425
  last_name: Kleinhanns
- first_name: Seungho
  full_name: Lee, Seungho
  id: BB243B88-D767-11E9-B658-BC13E6697425
  last_name: Lee
  orcid: 0000-0002-6962-8598
- first_name: Jordi
  full_name: Llorca, Jordi
  last_name: Llorca
- first_name: Oana
  full_name: Cojocaru‐Mirédin, Oana
  last_name: Cojocaru‐Mirédin
- first_name: Maria
  full_name: Ibáñez, Maria
  id: 43C61214-F248-11E8-B48F-1D18A9856A87
  last_name: Ibáñez
  orcid: 0000-0001-5013-2843
citation:
  ama: 'Liu Y, Calcabrini M, Yu Y, et al. The importance of surface adsorbates in
    solution‐processed thermoelectric materials: The case of SnSe. <i>Advanced Materials</i>.
    2021;33(52). doi:<a href="https://doi.org/10.1002/adma.202106858">10.1002/adma.202106858</a>'
  apa: 'Liu, Y., Calcabrini, M., Yu, Y., Genç, A., Chang, C., Costanzo, T., … Ibáñez,
    M. (2021). The importance of surface adsorbates in solution‐processed thermoelectric
    materials: The case of SnSe. <i>Advanced Materials</i>. Wiley. <a href="https://doi.org/10.1002/adma.202106858">https://doi.org/10.1002/adma.202106858</a>'
  chicago: 'Liu, Yu, Mariano Calcabrini, Yuan Yu, Aziz Genç, Cheng Chang, Tommaso
    Costanzo, Tobias Kleinhanns, et al. “The Importance of Surface Adsorbates in Solution‐processed
    Thermoelectric Materials: The Case of SnSe.” <i>Advanced Materials</i>. Wiley,
    2021. <a href="https://doi.org/10.1002/adma.202106858">https://doi.org/10.1002/adma.202106858</a>.'
  ieee: 'Y. Liu <i>et al.</i>, “The importance of surface adsorbates in solution‐processed
    thermoelectric materials: The case of SnSe,” <i>Advanced Materials</i>, vol. 33,
    no. 52. Wiley, 2021.'
  ista: 'Liu Y, Calcabrini M, Yu Y, Genç A, Chang C, Costanzo T, Kleinhanns T, Lee
    S, Llorca J, Cojocaru‐Mirédin O, Ibáñez M. 2021. The importance of surface adsorbates
    in solution‐processed thermoelectric materials: The case of SnSe. Advanced Materials.
    33(52), 2106858.'
  mla: 'Liu, Yu, et al. “The Importance of Surface Adsorbates in Solution‐processed
    Thermoelectric Materials: The Case of SnSe.” <i>Advanced Materials</i>, vol. 33,
    no. 52, 2106858, Wiley, 2021, doi:<a href="https://doi.org/10.1002/adma.202106858">10.1002/adma.202106858</a>.'
  short: Y. Liu, M. Calcabrini, Y. Yu, A. Genç, C. Chang, T. Costanzo, T. Kleinhanns,
    S. Lee, J. Llorca, O. Cojocaru‐Mirédin, M. Ibáñez, Advanced Materials 33 (2021).
date_created: 2021-10-11T20:07:24Z
date_published: 2021-12-29T00:00:00Z
date_updated: 2023-08-14T07:25:27Z
day: '29'
ddc:
- '620'
department:
- _id: EM-Fac
- _id: MaIb
doi: 10.1002/adma.202106858
ec_funded: 1
external_id:
  isi:
  - '000709899300001'
  pmid:
  - '34626034'
file:
- access_level: open_access
  checksum: 990bccc527c64d85cf1c97885110b5f4
  content_type: application/pdf
  creator: cchlebak
  date_created: 2022-02-03T13:16:14Z
  date_updated: 2022-02-03T13:16:14Z
  file_id: '10720'
  file_name: 2021_AdvancedMaterials_Liu.pdf
  file_size: 5595666
  relation: main_file
  success: 1
file_date_updated: 2022-02-03T13:16:14Z
has_accepted_license: '1'
intvolume: '        33'
isi: 1
issue: '52'
keyword:
- mechanical engineering
- mechanics of materials
- general materials science
language:
- iso: eng
month: '12'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '665385'
  name: International IST Doctoral Program
- _id: 260C2330-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '754411'
  name: ISTplus - Postdoctoral Fellowships
- _id: 9B8804FC-BA93-11EA-9121-9846C619BF3A
  grant_number: M02889
  name: Bottom-up Engineering for Thermoelectric Applications
- _id: 9B8F7476-BA93-11EA-9121-9846C619BF3A
  name: 'HighTE: The Werner Siemens Laboratory for the High Throughput Discovery of
    Semiconductors for Waste Heat Recovery'
publication: Advanced Materials
publication_identifier:
  eissn:
  - 1521-4095
  issn:
  - 0935-9648
publication_status: published
publisher: Wiley
quality_controlled: '1'
related_material:
  record:
  - id: '12885'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: 'The importance of surface adsorbates in solution‐processed thermoelectric
  materials: The case of SnSe'
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 33
year: '2021'
...
---
_id: '9447'
abstract:
- lang: eng
  text: 'Lithium bis(trifluoromethylsulfonyl)imide (LiTFSI) based water-in-salt electrolytes
    (WiSEs) has recently emerged as a new promising class of electrolytes, primarily
    owing to their wide electrochemical stability windows (~3–4 V), that by far exceed
    the thermodynamic stability window of water (1.23 V). Upon increasing the salt
    concentration towards superconcentration the onset of the oxygen evolution reaction
    (OER) shifts more significantly than the hydrogen evolution reaction (HER) does.
    The OER shift has been explained by the accumulation of hydrophobic anions blocking
    water access to the electrode surface, hence by double layer theory. Here we demonstrate
    that the processes during oxidation are much more complex, involving OER, carbon
    and salt decomposition by OER intermediates, and salt precipitation upon local
    oversaturation. The positive shift in the onset potential of oxidation currents
    was elucidated by combining several advanced analysis techniques: rotating ring-disk
    electrode voltammetry, online electrochemical mass spectrometry, and X-ray photoelectron
    spectroscopy, using both dilute and superconcentrated electrolytes. The results
    demonstrate the importance of reactive OER intermediates and surface films for
    electrolyte and electrode stability and motivate further studies of the nature
    of the electrode.'
article_number: '050550'
article_processing_charge: No
author:
- first_name: Marion
  full_name: Maffre, Marion
  last_name: Maffre
- first_name: Roza
  full_name: Bouchal, Roza
  last_name: Bouchal
- first_name: Stefan Alexander
  full_name: Freunberger, Stefan Alexander
  id: A8CA28E6-CE23-11E9-AD2D-EC27E6697425
  last_name: Freunberger
  orcid: 0000-0003-2902-5319
- first_name: Niklas
  full_name: Lindahl, Niklas
  last_name: Lindahl
- first_name: Patrik
  full_name: Johansson, Patrik
  last_name: Johansson
- first_name: Frédéric
  full_name: Favier, Frédéric
  last_name: Favier
- first_name: Olivier
  full_name: Fontaine, Olivier
  last_name: Fontaine
- first_name: Daniel
  full_name: Bélanger, Daniel
  last_name: Bélanger
citation:
  ama: Maffre M, Bouchal R, Freunberger SA, et al. Investigation of electrochemical
    and chemical processes occurring at positive potentials in “Water-in-Salt” electrolytes.
    <i>Journal of The Electrochemical Society</i>. 2021;168(5). doi:<a href="https://doi.org/10.1149/1945-7111/ac0300">10.1149/1945-7111/ac0300</a>
  apa: Maffre, M., Bouchal, R., Freunberger, S. A., Lindahl, N., Johansson, P., Favier,
    F., … Bélanger, D. (2021). Investigation of electrochemical and chemical processes
    occurring at positive potentials in “Water-in-Salt” electrolytes. <i>Journal of
    The Electrochemical Society</i>. IOP Publishing. <a href="https://doi.org/10.1149/1945-7111/ac0300">https://doi.org/10.1149/1945-7111/ac0300</a>
  chicago: Maffre, Marion, Roza Bouchal, Stefan Alexander Freunberger, Niklas Lindahl,
    Patrik Johansson, Frédéric Favier, Olivier Fontaine, and Daniel Bélanger. “Investigation
    of Electrochemical and Chemical Processes Occurring at Positive Potentials in
    ‘Water-in-Salt’ Electrolytes.” <i>Journal of The Electrochemical Society</i>.
    IOP Publishing, 2021. <a href="https://doi.org/10.1149/1945-7111/ac0300">https://doi.org/10.1149/1945-7111/ac0300</a>.
  ieee: M. Maffre <i>et al.</i>, “Investigation of electrochemical and chemical processes
    occurring at positive potentials in ‘Water-in-Salt’ electrolytes,” <i>Journal
    of The Electrochemical Society</i>, vol. 168, no. 5. IOP Publishing, 2021.
  ista: Maffre M, Bouchal R, Freunberger SA, Lindahl N, Johansson P, Favier F, Fontaine
    O, Bélanger D. 2021. Investigation of electrochemical and chemical processes occurring
    at positive potentials in “Water-in-Salt” electrolytes. Journal of The Electrochemical
    Society. 168(5), 050550.
  mla: Maffre, Marion, et al. “Investigation of Electrochemical and Chemical Processes
    Occurring at Positive Potentials in ‘Water-in-Salt’ Electrolytes.” <i>Journal
    of The Electrochemical Society</i>, vol. 168, no. 5, 050550, IOP Publishing, 2021,
    doi:<a href="https://doi.org/10.1149/1945-7111/ac0300">10.1149/1945-7111/ac0300</a>.
  short: M. Maffre, R. Bouchal, S.A. Freunberger, N. Lindahl, P. Johansson, F. Favier,
    O. Fontaine, D. Bélanger, Journal of The Electrochemical Society 168 (2021).
date_created: 2021-06-03T09:58:38Z
date_published: 2021-05-01T00:00:00Z
date_updated: 2023-09-05T13:25:30Z
day: '01'
department:
- _id: StFr
doi: 10.1149/1945-7111/ac0300
external_id:
  isi:
  - '000657724200001'
intvolume: '       168'
isi: 1
issue: '5'
keyword:
- Renewable Energy
- Sustainability and the Environment
- Electrochemistry
- Materials Chemistry
- Electronic
- Optical and Magnetic Materials
- Surfaces
- Coatings and Films
- Condensed Matter Physics
language:
- iso: eng
month: '05'
oa_version: None
publication: Journal of The Electrochemical Society
publication_identifier:
  eissn:
  - 1945-7111
  issn:
  - 0013-4651
publication_status: published
publisher: IOP Publishing
quality_controlled: '1'
status: public
title: Investigation of electrochemical and chemical processes occurring at positive
  potentials in “Water-in-Salt” electrolytes
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 168
year: '2021'
...
---
_id: '9978'
abstract:
- lang: eng
  text: Redox mediators could catalyse otherwise slow and energy-inefficient cycling
    of Li-S and Li-O 2 batteries by shuttling electrons/holes between the electrode
    and the solid insulating storage materials. For mediators to work efficiently
    they need to oxidize the solid with fast kinetics yet the lowest possible overpotential.
    Here, we found that when the redox potentials of mediators are tuned via, e.g.,
    Li + concentration in the electrolyte, they exhibit distinct threshold potentials,
    where the kinetics accelerate several-fold within a range as small as 10 mV. This
    phenomenon is independent of types of mediators and electrolyte. The acceleration
    originates from the overpotentials required to activate fast Li + /e – extraction
    and the following chemical step at specific abundant surface facets. Efficient
    redox catalysis at insulating solids requires therefore carefully considering
    the surface conditions of the storage materials and electrolyte-dependent redox
    potentials, which may be tuned by salt concentrations or solvents.
acknowledgement: 'This work was financially supported by the National Natural Science
  Foundation of China (51773092, 21975124, 11874254, 51802187, U2030206). S.A.F. is
  indebted to IST Austria for support. '
article_processing_charge: No
author:
- first_name: Deqing
  full_name: Cao, Deqing
  last_name: Cao
- first_name: Xiaoxiao
  full_name: Shen, Xiaoxiao
  last_name: Shen
- first_name: Aiping
  full_name: Wang, Aiping
  last_name: Wang
- first_name: Fengjiao
  full_name: Yu, Fengjiao
  last_name: Yu
- first_name: Yuping
  full_name: Wu, Yuping
  last_name: Wu
- first_name: Siqi
  full_name: Shi, Siqi
  last_name: Shi
- first_name: Stefan Alexander
  full_name: Freunberger, Stefan Alexander
  id: A8CA28E6-CE23-11E9-AD2D-EC27E6697425
  last_name: Freunberger
  orcid: 0000-0003-2902-5319
- first_name: Yuhui
  full_name: Chen, Yuhui
  last_name: Chen
citation:
  ama: Cao D, Shen X, Wang A, et al. Sharp kinetic acceleration potentials during
    mediated redox catalysis of insulators. <i>Research Square</i>. doi:<a href="https://doi.org/10.21203/rs.3.rs-750965/v1">10.21203/rs.3.rs-750965/v1</a>
  apa: Cao, D., Shen, X., Wang, A., Yu, F., Wu, Y., Shi, S., … Chen, Y. (n.d.). Sharp
    kinetic acceleration potentials during mediated redox catalysis of insulators.
    <i>Research Square</i>. Research Square. <a href="https://doi.org/10.21203/rs.3.rs-750965/v1">https://doi.org/10.21203/rs.3.rs-750965/v1</a>
  chicago: Cao, Deqing, Xiaoxiao Shen, Aiping Wang, Fengjiao Yu, Yuping Wu, Siqi Shi,
    Stefan Alexander Freunberger, and Yuhui Chen. “Sharp Kinetic Acceleration Potentials
    during Mediated Redox Catalysis of Insulators.” <i>Research Square</i>. Research
    Square, n.d. <a href="https://doi.org/10.21203/rs.3.rs-750965/v1">https://doi.org/10.21203/rs.3.rs-750965/v1</a>.
  ieee: D. Cao <i>et al.</i>, “Sharp kinetic acceleration potentials during mediated
    redox catalysis of insulators,” <i>Research Square</i>. Research Square.
  ista: Cao D, Shen X, Wang A, Yu F, Wu Y, Shi S, Freunberger SA, Chen Y. Sharp kinetic
    acceleration potentials during mediated redox catalysis of insulators. Research
    Square, <a href="https://doi.org/10.21203/rs.3.rs-750965/v1">10.21203/rs.3.rs-750965/v1</a>.
  mla: Cao, Deqing, et al. “Sharp Kinetic Acceleration Potentials during Mediated
    Redox Catalysis of Insulators.” <i>Research Square</i>, Research Square, doi:<a
    href="https://doi.org/10.21203/rs.3.rs-750965/v1">10.21203/rs.3.rs-750965/v1</a>.
  short: D. Cao, X. Shen, A. Wang, F. Yu, Y. Wu, S. Shi, S.A. Freunberger, Y. Chen,
    Research Square (n.d.).
date_created: 2021-08-31T12:54:16Z
date_published: 2021-08-18T00:00:00Z
date_updated: 2023-10-17T13:06:29Z
day: '18'
ddc:
- '541'
department:
- _id: StFr
doi: 10.21203/rs.3.rs-750965/v1
file:
- access_level: open_access
  checksum: 1878e91c29d5769ed5a827b0b7addf00
  content_type: application/pdf
  creator: cchlebak
  date_created: 2021-08-31T14:02:19Z
  date_updated: 2021-08-31T14:02:19Z
  file_id: '9979'
  file_name: 2021_ResearchSquare_Cao.pdf
  file_size: 1019662
  relation: main_file
  success: 1
file_date_updated: 2021-08-31T14:02:19Z
has_accepted_license: '1'
keyword:
- Catalysis
- Energy engineering
- Materials theory and modeling
language:
- iso: eng
month: '08'
oa: 1
oa_version: Preprint
page: '21'
publication: Research Square
publication_identifier:
  eissn:
  - 2693-5015
publication_status: submitted
publisher: Research Square
related_material:
  record:
  - id: '10813'
    relation: later_version
    status: public
status: public
title: Sharp kinetic acceleration potentials during mediated redox catalysis of insulators
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: preprint
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2021'
...
---
_id: '10858'
abstract:
- lang: eng
  text: The cost-effective conversion of low-grade heat into electricity using thermoelectric
    devices requires developing alternative materials and material processing technologies
    able to reduce the currently high device manufacturing costs. In this direction,
    thermoelectric materials that do not rely on rare or toxic elements such as tellurium
    or lead need to be produced using high-throughput technologies not involving high
    temperatures and long processes. Bi2Se3 is an obvious possible Te-free alternative
    to Bi2Te3 for ambient temperature thermoelectric applications, but its performance
    is still low for practical applications, and additional efforts toward finding
    proper dopants are required. Here, we report a scalable method to produce Bi2Se3
    nanosheets at low synthesis temperatures. We studied the influence of different
    dopants on the thermoelectric properties of this material. Among the elements
    tested, we demonstrated that Sn doping resulted in the best performance. Sn incorporation
    resulted in a significant improvement to the Bi2Se3 Seebeck coefficient and a
    reduction in the thermal conductivity in the direction of the hot-press axis,
    resulting in an overall 60% improvement in the thermoelectric figure of merit
    of Bi2Se3.
acknowledgement: "M.L., Y.Z., T.Z. and K.X. thank the China Scholarship Council for
  their scholarship\r\nsupport. Y.L. acknowledges funding from the European Union’s
  Horizon 2020 research and\r\ninnovation program under the Marie Sklodowska-Curie
  grant agreement No. 754411. J.L. thanks the ICREA Academia program and projects
  MICINN/FEDER RTI2018-093996-B-C31 and G.C. 2017 SGR 128. ICN2 acknowledges funding
  from the Generalitat de Catalunya 2017 SGR 327 and the Spanish MINECO ENE2017-85087-C3."
article_number: '1827'
article_processing_charge: No
article_type: original
author:
- first_name: Mengyao
  full_name: Li, Mengyao
  last_name: Li
- first_name: Yu
  full_name: Zhang, Yu
  last_name: Zhang
- first_name: Ting
  full_name: Zhang, Ting
  last_name: Zhang
- first_name: Yong
  full_name: Zuo, Yong
  last_name: Zuo
- first_name: Ke
  full_name: Xiao, Ke
  last_name: Xiao
- first_name: Jordi
  full_name: Arbiol, Jordi
  last_name: Arbiol
- first_name: Jordi
  full_name: Llorca, Jordi
  last_name: Llorca
- first_name: Yu
  full_name: Liu, Yu
  id: 2A70014E-F248-11E8-B48F-1D18A9856A87
  last_name: Liu
  orcid: 0000-0001-7313-6740
- first_name: Andreu
  full_name: Cabot, Andreu
  last_name: Cabot
citation:
  ama: Li M, Zhang Y, Zhang T, et al. Enhanced thermoelectric performance of n-type
    Bi2Se3 nanosheets through Sn doping. <i>Nanomaterials</i>. 2021;11(7). doi:<a
    href="https://doi.org/10.3390/nano11071827">10.3390/nano11071827</a>
  apa: Li, M., Zhang, Y., Zhang, T., Zuo, Y., Xiao, K., Arbiol, J., … Cabot, A. (2021).
    Enhanced thermoelectric performance of n-type Bi2Se3 nanosheets through Sn doping.
    <i>Nanomaterials</i>. MDPI. <a href="https://doi.org/10.3390/nano11071827">https://doi.org/10.3390/nano11071827</a>
  chicago: Li, Mengyao, Yu Zhang, Ting Zhang, Yong Zuo, Ke Xiao, Jordi Arbiol, Jordi
    Llorca, Yu Liu, and Andreu Cabot. “Enhanced Thermoelectric Performance of N-Type
    Bi2Se3 Nanosheets through Sn Doping.” <i>Nanomaterials</i>. MDPI, 2021. <a href="https://doi.org/10.3390/nano11071827">https://doi.org/10.3390/nano11071827</a>.
  ieee: M. Li <i>et al.</i>, “Enhanced thermoelectric performance of n-type Bi2Se3
    nanosheets through Sn doping,” <i>Nanomaterials</i>, vol. 11, no. 7. MDPI, 2021.
  ista: Li M, Zhang Y, Zhang T, Zuo Y, Xiao K, Arbiol J, Llorca J, Liu Y, Cabot A.
    2021. Enhanced thermoelectric performance of n-type Bi2Se3 nanosheets through
    Sn doping. Nanomaterials. 11(7), 1827.
  mla: Li, Mengyao, et al. “Enhanced Thermoelectric Performance of N-Type Bi2Se3 Nanosheets
    through Sn Doping.” <i>Nanomaterials</i>, vol. 11, no. 7, 1827, MDPI, 2021, doi:<a
    href="https://doi.org/10.3390/nano11071827">10.3390/nano11071827</a>.
  short: M. Li, Y. Zhang, T. Zhang, Y. Zuo, K. Xiao, J. Arbiol, J. Llorca, Y. Liu,
    A. Cabot, Nanomaterials 11 (2021).
date_created: 2022-03-18T09:45:02Z
date_published: 2021-07-14T00:00:00Z
date_updated: 2023-08-17T07:08:30Z
day: '14'
ddc:
- '540'
department:
- _id: MaIb
doi: 10.3390/nano11071827
ec_funded: 1
external_id:
  isi:
  - '000676570000001'
file:
- access_level: open_access
  checksum: f28a8b5cf80f5605828359bb398463b0
  content_type: application/pdf
  creator: dernst
  date_created: 2022-03-18T09:53:15Z
  date_updated: 2022-03-18T09:53:15Z
  file_id: '10859'
  file_name: 2021_Nanomaterials_Li.pdf
  file_size: 4867547
  relation: main_file
  success: 1
file_date_updated: 2022-03-18T09:53:15Z
has_accepted_license: '1'
intvolume: '        11'
isi: 1
issue: '7'
keyword:
- General Materials Science
- General Chemical Engineering
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
project:
- _id: 260C2330-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '754411'
  name: ISTplus - Postdoctoral Fellowships
publication: Nanomaterials
publication_identifier:
  issn:
  - 2079-4991
publication_status: published
publisher: MDPI
quality_controlled: '1'
scopus_import: '1'
status: public
title: Enhanced thermoelectric performance of n-type Bi2Se3 nanosheets through Sn
  doping
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 11
year: '2021'
...
---
_id: '8592'
abstract:
- lang: eng
  text: Glioblastoma is the most malignant cancer in the brain and currently incurable.
    It is urgent to identify effective targets for this lethal disease. Inhibition
    of such targets should suppress the growth of cancer cells and, ideally also precancerous
    cells for early prevention, but minimally affect their normal counterparts. Using
    genetic mouse models with neural stem cells (NSCs) or oligodendrocyte precursor
    cells (OPCs) as the cells‐of‐origin/mutation, it is shown that the susceptibility
    of cells within the development hierarchy of glioma to the knockout of insulin‐like
    growth factor I receptor (IGF1R) is determined not only by their oncogenic states,
    but also by their cell identities/states. Knockout of IGF1R selectively disrupts
    the growth of mutant and transformed, but not normal OPCs, or NSCs. The desirable
    outcome of IGF1R knockout on cell growth requires the mutant cells to commit to
    the OPC identity regardless of its development hierarchical status. At the molecular
    level, oncogenic mutations reprogram the cellular network of OPCs and force them
    to depend more on IGF1R for their growth. A new‐generation brain‐penetrable, orally
    available IGF1R inhibitor harnessing tumor OPCs in the brain is also developed.
    The findings reveal the cellular window of IGF1R targeting and establish IGF1R
    as an effective target for the prevention and treatment of glioblastoma.
acknowledgement: The authors thank Drs. J. Eisen, QR. Lu, S. Duan, Z‐H. Li, W. Mo,
  and Q. Wu for their critical comments on the manuscript. They also thank Dr. H.
  Zong for providing the CKO_NG2‐CreER model. This work is supported by the National
  Key Research and Development Program of China, Stem Cell and Translational Research
  (2016YFA0101201 to C.L., 2016YFA0100303 to Y.J.W.), the National Natural Science
  Foundation of China (81673035 and 81972915 to C.L., 81472722 to Y.J.W.), the Science
  Foundation for Distinguished Young Scientists of Zhejiang Province (LR17H160001
  to C.L.), Fundamental Research Funds for the Central Universities (2016QNA7023 and
  2017QNA7028 to C.L.) and the Thousand Talent Program for Young Outstanding Scientists,
  China (to C.L.), IST Austria institutional funds (to S.H.), European Research Council
  (ERC) under the European Union's Horizon 2020 research and innovation programme
  (725780 LinPro to S.H.). C.L. is a scholar of K. C. Wong Education Foundation.
article_number: '2001724'
article_processing_charge: No
article_type: original
author:
- first_name: Anhao
  full_name: Tian, Anhao
  last_name: Tian
- first_name: Bo
  full_name: Kang, Bo
  last_name: Kang
- first_name: Baizhou
  full_name: Li, Baizhou
  last_name: Li
- first_name: Biying
  full_name: Qiu, Biying
  last_name: Qiu
- first_name: Wenhong
  full_name: Jiang, Wenhong
  last_name: Jiang
- first_name: Fangjie
  full_name: Shao, Fangjie
  last_name: Shao
- first_name: Qingqing
  full_name: Gao, Qingqing
  last_name: Gao
- first_name: Rui
  full_name: Liu, Rui
  last_name: Liu
- first_name: Chengwei
  full_name: Cai, Chengwei
  last_name: Cai
- first_name: Rui
  full_name: Jing, Rui
  last_name: Jing
- first_name: Wei
  full_name: Wang, Wei
  last_name: Wang
- first_name: Pengxiang
  full_name: Chen, Pengxiang
  last_name: Chen
- first_name: Qinghui
  full_name: Liang, Qinghui
  last_name: Liang
- first_name: Lili
  full_name: Bao, Lili
  last_name: Bao
- first_name: Jianghong
  full_name: Man, Jianghong
  last_name: Man
- first_name: Yan
  full_name: Wang, Yan
  last_name: Wang
- first_name: Yu
  full_name: Shi, Yu
  last_name: Shi
- first_name: Jin
  full_name: Li, Jin
  last_name: Li
- first_name: Minmin
  full_name: Yang, Minmin
  last_name: Yang
- first_name: Lisha
  full_name: Wang, Lisha
  last_name: Wang
- first_name: Jianmin
  full_name: Zhang, Jianmin
  last_name: Zhang
- first_name: Simon
  full_name: Hippenmeyer, Simon
  id: 37B36620-F248-11E8-B48F-1D18A9856A87
  last_name: Hippenmeyer
  orcid: 0000-0003-2279-1061
- first_name: Junming
  full_name: Zhu, Junming
  last_name: Zhu
- first_name: Xiuwu
  full_name: Bian, Xiuwu
  last_name: Bian
- first_name: Ying‐Jie
  full_name: Wang, Ying‐Jie
  last_name: Wang
- first_name: Chong
  full_name: Liu, Chong
  last_name: Liu
citation:
  ama: Tian A, Kang B, Li B, et al. Oncogenic state and cell identity combinatorially
    dictate the susceptibility of cells within glioma development hierarchy to IGF1R
    targeting. <i>Advanced Science</i>. 2020;7(21). doi:<a href="https://doi.org/10.1002/advs.202001724">10.1002/advs.202001724</a>
  apa: Tian, A., Kang, B., Li, B., Qiu, B., Jiang, W., Shao, F., … Liu, C. (2020).
    Oncogenic state and cell identity combinatorially dictate the susceptibility of
    cells within glioma development hierarchy to IGF1R targeting. <i>Advanced Science</i>.
    Wiley. <a href="https://doi.org/10.1002/advs.202001724">https://doi.org/10.1002/advs.202001724</a>
  chicago: Tian, Anhao, Bo Kang, Baizhou Li, Biying Qiu, Wenhong Jiang, Fangjie Shao,
    Qingqing Gao, et al. “Oncogenic State and Cell Identity Combinatorially Dictate
    the Susceptibility of Cells within Glioma Development Hierarchy to IGF1R Targeting.”
    <i>Advanced Science</i>. Wiley, 2020. <a href="https://doi.org/10.1002/advs.202001724">https://doi.org/10.1002/advs.202001724</a>.
  ieee: A. Tian <i>et al.</i>, “Oncogenic state and cell identity combinatorially
    dictate the susceptibility of cells within glioma development hierarchy to IGF1R
    targeting,” <i>Advanced Science</i>, vol. 7, no. 21. Wiley, 2020.
  ista: Tian A, Kang B, Li B, Qiu B, Jiang W, Shao F, Gao Q, Liu R, Cai C, Jing R,
    Wang W, Chen P, Liang Q, Bao L, Man J, Wang Y, Shi Y, Li J, Yang M, Wang L, Zhang
    J, Hippenmeyer S, Zhu J, Bian X, Wang Y, Liu C. 2020. Oncogenic state and cell
    identity combinatorially dictate the susceptibility of cells within glioma development
    hierarchy to IGF1R targeting. Advanced Science. 7(21), 2001724.
  mla: Tian, Anhao, et al. “Oncogenic State and Cell Identity Combinatorially Dictate
    the Susceptibility of Cells within Glioma Development Hierarchy to IGF1R Targeting.”
    <i>Advanced Science</i>, vol. 7, no. 21, 2001724, Wiley, 2020, doi:<a href="https://doi.org/10.1002/advs.202001724">10.1002/advs.202001724</a>.
  short: A. Tian, B. Kang, B. Li, B. Qiu, W. Jiang, F. Shao, Q. Gao, R. Liu, C. Cai,
    R. Jing, W. Wang, P. Chen, Q. Liang, L. Bao, J. Man, Y. Wang, Y. Shi, J. Li, M.
    Yang, L. Wang, J. Zhang, S. Hippenmeyer, J. Zhu, X. Bian, Y. Wang, C. Liu, Advanced
    Science 7 (2020).
date_created: 2020-10-01T09:44:13Z
date_published: 2020-11-04T00:00:00Z
date_updated: 2023-08-22T09:53:01Z
day: '04'
ddc:
- '570'
department:
- _id: SiHi
doi: 10.1002/advs.202001724
ec_funded: 1
external_id:
  isi:
  - '000573860700001'
file:
- access_level: open_access
  checksum: 92818c23ecc70e35acfa671f3cfb9909
  content_type: application/pdf
  creator: dernst
  date_created: 2020-12-10T14:07:24Z
  date_updated: 2020-12-10T14:07:24Z
  file_id: '8938'
  file_name: 2020_AdvScience_Tian.pdf
  file_size: 7835833
  relation: main_file
  success: 1
file_date_updated: 2020-12-10T14:07:24Z
has_accepted_license: '1'
intvolume: '         7'
isi: 1
issue: '21'
keyword:
- General Engineering
- General Physics and Astronomy
- General Materials Science
- Medicine (miscellaneous)
- General Chemical Engineering
- Biochemistry
- Genetics and Molecular Biology (miscellaneous)
language:
- iso: eng
month: '11'
oa: 1
oa_version: Published Version
project:
- _id: 260018B0-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '725780'
  name: Principles of Neural Stem Cell Lineage Progression in Cerebral Cortex Development
publication: Advanced Science
publication_identifier:
  issn:
  - 2198-3844
publication_status: published
publisher: Wiley
quality_controlled: '1'
status: public
title: Oncogenic state and cell identity combinatorially dictate the susceptibility
  of cells within glioma development hierarchy to IGF1R targeting
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 7
year: '2020'
...
---
_id: '9069'
abstract:
- lang: eng
  text: In the quest for alternate and efficient electrode materials, ternary metal
    electrocatalysts (TMEs), part of the perovskite family, were synthesized and tested
    for methanol electro-oxidation in alkaline media. La0.5Ca0.5MO3 (M = Ni, Co, or
    Mn) was synthesized via sol-gel method. X-ray diffraction analysis revealed that
    the perovskite crystal structure possesses characteristic sharp and crystalline
    peaks for all synthesized ternary electrocatalysts. The average particle size
    calculated using Debye–Scherrer equation was in the order of La0.5Ca0.5NiO3 (LCNO)
    > La0.5Ca0.5CoO3 (LCCO)> La0.5Ca0.5MnO3 (LCMO). The elemental composition of as
    prepared sample, LCCO was investigated via x-ray fluorescence spectroscopy. The
    qualitative and quantitative analysis revealed the presence of La, Ca and Co in
    parent crystal structure with percentage compositions of 9.0, 3.12 and 87.82%
    respectively. The particle size distribution was homogenous, as determined by
    scanning electron and transmission electron microscopes. The electrocatalytic
    activity of the synthesized ternary electrocatalysts was studied electrochemically
    by cyclic voltammetry. The calculated diffusion coefficient values showed that
    electrode surface of LCNO and LCCO have limited efficiency for diffusion related
    phenomenon. The heterogeneous rate constants inferred better electrode kinetics
    of LCCO and LCNO which exhibited good electrocatalytic behavior; sharp anodic
    peaks were observed in the potential range of +0.3 to 0.6 V and +0.6 to 0.8 V,
    respectively. Methanol electro-oxidation was found minimal in case of LCMO sample.
    We have observed that Co substitution at B-site of perovskite electrode materials
    attains better electrochemical properties, thus in relation with reported literature.
article_number: 1250g6
article_processing_charge: No
article_type: original
author:
- first_name: Tayyaba
  full_name: Hussain, Tayyaba
  last_name: Hussain
- first_name: Muhammad
  full_name: Nauman, Muhammad
  id: 32c21954-2022-11eb-9d5f-af9f93c24e71
  last_name: Nauman
  orcid: 0000-0002-2111-4846
- first_name: Sana
  full_name: Sabahat, Sana
  last_name: Sabahat
- first_name: Saira
  full_name: Arif, Saira
  last_name: Arif
citation:
  ama: Hussain T, Nauman M, Sabahat S, Arif S. Synthesis of ternary electrocatalysts
    for exploration of methanol electro-oxidation in alkaline media. <i>Materials
    Research Express</i>. 2020;6(12). doi:<a href="https://doi.org/10.1088/2053-1591/ab6886">10.1088/2053-1591/ab6886</a>
  apa: Hussain, T., Nauman, M., Sabahat, S., &#38; Arif, S. (2020). Synthesis of ternary
    electrocatalysts for exploration of methanol electro-oxidation in alkaline media.
    <i>Materials Research Express</i>. IOP Publishing. <a href="https://doi.org/10.1088/2053-1591/ab6886">https://doi.org/10.1088/2053-1591/ab6886</a>
  chicago: Hussain, Tayyaba, Muhammad Nauman, Sana Sabahat, and Saira Arif. “Synthesis
    of Ternary Electrocatalysts for Exploration of Methanol Electro-Oxidation in Alkaline
    Media.” <i>Materials Research Express</i>. IOP Publishing, 2020. <a href="https://doi.org/10.1088/2053-1591/ab6886">https://doi.org/10.1088/2053-1591/ab6886</a>.
  ieee: T. Hussain, M. Nauman, S. Sabahat, and S. Arif, “Synthesis of ternary electrocatalysts
    for exploration of methanol electro-oxidation in alkaline media,” <i>Materials
    Research Express</i>, vol. 6, no. 12. IOP Publishing, 2020.
  ista: Hussain T, Nauman M, Sabahat S, Arif S. 2020. Synthesis of ternary electrocatalysts
    for exploration of methanol electro-oxidation in alkaline media. Materials Research
    Express. 6(12), 1250g6.
  mla: Hussain, Tayyaba, et al. “Synthesis of Ternary Electrocatalysts for Exploration
    of Methanol Electro-Oxidation in Alkaline Media.” <i>Materials Research Express</i>,
    vol. 6, no. 12, 1250g6, IOP Publishing, 2020, doi:<a href="https://doi.org/10.1088/2053-1591/ab6886">10.1088/2053-1591/ab6886</a>.
  short: T. Hussain, M. Nauman, S. Sabahat, S. Arif, Materials Research Express 6
    (2020).
date_created: 2021-02-02T15:53:57Z
date_published: 2020-01-15T00:00:00Z
date_updated: 2021-02-04T07:21:35Z
day: '15'
doi: 10.1088/2053-1591/ab6886
extern: '1'
intvolume: '         6'
issue: '12'
keyword:
- Electronic
- Optical and Magnetic Materials
- Surfaces
- Coatings and Films
- Polymers and Plastics
- Metals and Alloys
- Biomaterials
language:
- iso: eng
month: '01'
oa_version: None
publication: Materials Research Express
publication_identifier:
  issn:
  - 2053-1591
publication_status: published
publisher: IOP Publishing
quality_controlled: '1'
status: public
title: Synthesis of ternary electrocatalysts for exploration of methanol electro-oxidation
  in alkaline media
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 6
year: '2020'
...
---
_id: '8101'
abstract:
- lang: eng
  text: By rigorously accounting for mesoscale spatial correlations in donor/acceptor
    surface properties, we develop a scale-spanning model for same-material tribocharging.
    We find that mesoscale correlations affect not only the magnitude of charge transfer
    but also the fluctuations—suppressing otherwise overwhelming charge-transfer variability
    that is not observed experimentally. We furthermore propose a generic theoretical
    mechanism by which the mesoscale features might emerge, which is qualitatively
    consistent with other proposals in the literature.
acknowledgement: "We would like to thank Philip Born, Bartosz Grzybowski, Tarik Baytekin,
  and Bilge Baytekin for helpful discussions.\r\nThis project has received funding
  from the European Unions Horizon 2020 research and innovation programme under the
  Marie Skłodowska-Curie Grant Agreement No. 754411."
article_number: '082602'
article_processing_charge: Yes
article_type: original
arxiv: 1
author:
- first_name: Galien M
  full_name: Grosjean, Galien M
  id: 0C5FDA4A-9CF6-11E9-8939-FF05E6697425
  last_name: Grosjean
  orcid: 0000-0001-5154-417X
- first_name: Sebastian
  full_name: Wald, Sebastian
  id: 133F200A-B015-11E9-AD41-0EDAE5697425
  last_name: Wald
- first_name: Juan Carlos A
  full_name: Sobarzo Ponce, Juan Carlos A
  id: 4B807D68-AE37-11E9-AC72-31CAE5697425
  last_name: Sobarzo Ponce
- first_name: Scott R
  full_name: Waitukaitis, Scott R
  id: 3A1FFC16-F248-11E8-B48F-1D18A9856A87
  last_name: Waitukaitis
  orcid: 0000-0002-2299-3176
citation:
  ama: Grosjean GM, Wald S, Sobarzo Ponce JCA, Waitukaitis SR. Quantitatively consistent
    scale-spanning model for same-material tribocharging. <i>Physical Review Materials</i>.
    2020;4(8). doi:<a href="https://doi.org/10.1103/PhysRevMaterials.4.082602">10.1103/PhysRevMaterials.4.082602</a>
  apa: Grosjean, G. M., Wald, S., Sobarzo Ponce, J. C. A., &#38; Waitukaitis, S. R.
    (2020). Quantitatively consistent scale-spanning model for same-material tribocharging.
    <i>Physical Review Materials</i>. American Physical Society. <a href="https://doi.org/10.1103/PhysRevMaterials.4.082602">https://doi.org/10.1103/PhysRevMaterials.4.082602</a>
  chicago: Grosjean, Galien M, Sebastian Wald, Juan Carlos A Sobarzo Ponce, and Scott
    R Waitukaitis. “Quantitatively Consistent Scale-Spanning Model for Same-Material
    Tribocharging.” <i>Physical Review Materials</i>. American Physical Society, 2020.
    <a href="https://doi.org/10.1103/PhysRevMaterials.4.082602">https://doi.org/10.1103/PhysRevMaterials.4.082602</a>.
  ieee: G. M. Grosjean, S. Wald, J. C. A. Sobarzo Ponce, and S. R. Waitukaitis, “Quantitatively
    consistent scale-spanning model for same-material tribocharging,” <i>Physical
    Review Materials</i>, vol. 4, no. 8. American Physical Society, 2020.
  ista: Grosjean GM, Wald S, Sobarzo Ponce JCA, Waitukaitis SR. 2020. Quantitatively
    consistent scale-spanning model for same-material tribocharging. Physical Review
    Materials. 4(8), 082602.
  mla: Grosjean, Galien M., et al. “Quantitatively Consistent Scale-Spanning Model
    for Same-Material Tribocharging.” <i>Physical Review Materials</i>, vol. 4, no.
    8, 082602, American Physical Society, 2020, doi:<a href="https://doi.org/10.1103/PhysRevMaterials.4.082602">10.1103/PhysRevMaterials.4.082602</a>.
  short: G.M. Grosjean, S. Wald, J.C.A. Sobarzo Ponce, S.R. Waitukaitis, Physical
    Review Materials 4 (2020).
date_created: 2020-07-07T11:33:54Z
date_published: 2020-08-17T00:00:00Z
date_updated: 2023-08-22T08:41:32Z
day: '17'
ddc:
- '530'
department:
- _id: ScWa
doi: 10.1103/PhysRevMaterials.4.082602
ec_funded: 1
external_id:
  arxiv:
  - '2006.07120'
  isi:
  - '000561897000001'
file:
- access_level: open_access
  checksum: 288fef1eeb6540c6344bb8f7c8159dc9
  content_type: application/pdf
  creator: ggrosjea
  date_created: 2020-08-17T15:54:20Z
  date_updated: 2020-08-17T15:54:20Z
  file_id: '8277'
  file_name: Grosjean2020.pdf
  file_size: 853753
  relation: main_file
  success: 1
file_date_updated: 2020-08-17T15:54:20Z
has_accepted_license: '1'
intvolume: '         4'
isi: 1
issue: '8'
keyword:
- electric charge
- tribocharging
- soft matter
- granular materials
- polymers
language:
- iso: eng
month: '08'
oa: 1
oa_version: Published Version
project:
- _id: 260C2330-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '754411'
  name: ISTplus - Postdoctoral Fellowships
publication: Physical Review Materials
publication_identifier:
  issn:
  - 2475-9953
publication_status: published
publisher: American Physical Society
quality_controlled: '1'
related_material:
  record:
  - id: '12697'
    relation: popular_science
    status: public
scopus_import: '1'
status: public
title: Quantitatively consistent scale-spanning model for same-material tribocharging
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 4
year: '2020'
...
---
_id: '13363'
abstract:
- lang: eng
  text: Temporal activation of biological processes by visible light and subsequent
    return to an inactive state in the absence of light is an essential characteristic
    of photoreceptor cells. Inspired by these phenomena, light-responsive materials
    are very attractive due to the high spatiotemporal control of light irradiation,
    with light being able to precisely orchestrate processes repeatedly over many
    cycles. Herein, it is reported that light-driven proton transfer triggered by
    a merocyanine-based photoacid can be used to modulate the permeability of pH-responsive
    polymersomes through cyclic, temporally controlled protonation and deprotonation
    of the polymersome membrane. The membranes can undergo repeated light-driven swelling–contraction
    cycles without losing functional effectiveness. When applied to enzyme loaded-nanoreactors,
    this membrane responsiveness is used for the reversible control of enzymatic reactions.
    This combination of the merocyanine-based photoacid and pH-switchable nanoreactors
    results in rapidly responding and versatile supramolecular systems successfully
    used to switch enzymatic reactions ON and OFF on demand.
article_number: '2002135'
article_processing_charge: No
article_type: original
author:
- first_name: Silvia
  full_name: Moreno, Silvia
  last_name: Moreno
- first_name: Priyanka
  full_name: Sharan, Priyanka
  last_name: Sharan
- first_name: Johanna
  full_name: Engelke, Johanna
  last_name: Engelke
- first_name: Hannes
  full_name: Gumz, Hannes
  last_name: Gumz
- first_name: Susanne
  full_name: Boye, Susanne
  last_name: Boye
- first_name: Ulrich
  full_name: Oertel, Ulrich
  last_name: Oertel
- first_name: Peng
  full_name: Wang, Peng
  last_name: Wang
- first_name: Susanta
  full_name: Banerjee, Susanta
  last_name: Banerjee
- first_name: Rafal
  full_name: Klajn, Rafal
  id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b
  last_name: Klajn
- first_name: Brigitte
  full_name: Voit, Brigitte
  last_name: Voit
- first_name: Albena
  full_name: Lederer, Albena
  last_name: Lederer
- first_name: Dietmar
  full_name: Appelhans, Dietmar
  last_name: Appelhans
citation:
  ama: Moreno S, Sharan P, Engelke J, et al. Light‐driven proton transfer for cyclic
    and temporal switching of enzymatic nanoreactors. <i>Small</i>. 2020;16(37). doi:<a
    href="https://doi.org/10.1002/smll.202002135">10.1002/smll.202002135</a>
  apa: Moreno, S., Sharan, P., Engelke, J., Gumz, H., Boye, S., Oertel, U., … Appelhans,
    D. (2020). Light‐driven proton transfer for cyclic and temporal switching of enzymatic
    nanoreactors. <i>Small</i>. Wiley. <a href="https://doi.org/10.1002/smll.202002135">https://doi.org/10.1002/smll.202002135</a>
  chicago: Moreno, Silvia, Priyanka Sharan, Johanna Engelke, Hannes Gumz, Susanne
    Boye, Ulrich Oertel, Peng Wang, et al. “Light‐driven Proton Transfer for Cyclic
    and Temporal Switching of Enzymatic Nanoreactors.” <i>Small</i>. Wiley, 2020.
    <a href="https://doi.org/10.1002/smll.202002135">https://doi.org/10.1002/smll.202002135</a>.
  ieee: S. Moreno <i>et al.</i>, “Light‐driven proton transfer for cyclic and temporal
    switching of enzymatic nanoreactors,” <i>Small</i>, vol. 16, no. 37. Wiley, 2020.
  ista: Moreno S, Sharan P, Engelke J, Gumz H, Boye S, Oertel U, Wang P, Banerjee
    S, Klajn R, Voit B, Lederer A, Appelhans D. 2020. Light‐driven proton transfer
    for cyclic and temporal switching of enzymatic nanoreactors. Small. 16(37), 2002135.
  mla: Moreno, Silvia, et al. “Light‐driven Proton Transfer for Cyclic and Temporal
    Switching of Enzymatic Nanoreactors.” <i>Small</i>, vol. 16, no. 37, 2002135,
    Wiley, 2020, doi:<a href="https://doi.org/10.1002/smll.202002135">10.1002/smll.202002135</a>.
  short: S. Moreno, P. Sharan, J. Engelke, H. Gumz, S. Boye, U. Oertel, P. Wang, S.
    Banerjee, R. Klajn, B. Voit, A. Lederer, D. Appelhans, Small 16 (2020).
date_created: 2023-08-01T09:36:48Z
date_published: 2020-08-11T00:00:00Z
date_updated: 2023-08-07T10:11:41Z
day: '11'
doi: 10.1002/smll.202002135
extern: '1'
external_id:
  pmid:
  - '32783385'
intvolume: '        16'
issue: '37'
keyword:
- Biomaterials
- Biotechnology
- General Materials Science
- General Chemistry
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1002/smll.202002135
month: '08'
oa: 1
oa_version: Published Version
pmid: 1
publication: Small
publication_identifier:
  eissn:
  - 1613-6829
  issn:
  - 1613-6810
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: Light‐driven proton transfer for cyclic and temporal switching of enzymatic
  nanoreactors
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 16
year: '2020'
...
