---
_id: '15018'
abstract:
- lang: eng
text: The epitaxial growth of a strained Ge layer, which is a promising candidate
for the channel material of a hole spin qubit, has been demonstrated on 300 mm
Si wafers using commercially available Si0.3Ge0.7 strain relaxed buffer (SRB)
layers. The assessment of the layer and the interface qualities for a buried strained
Ge layer embedded in Si0.3Ge0.7 layers is reported. The XRD reciprocal space mapping
confirmed that the reduction of the growth temperature enables the 2-dimensional
growth of the Ge layer fully strained with respect to the Si0.3Ge0.7. Nevertheless,
dislocations at the top and/or bottom interface of the Ge layer were observed
by means of electron channeling contrast imaging, suggesting the importance of
the careful dislocation assessment. The interface abruptness does not depend on
the selection of the precursor gases, but it is strongly influenced by the growth
temperature which affects the coverage of the surface H-passivation. The mobility
of 2.7 × 105 cm2/Vs is promising, while the low percolation density of 3 × 1010
/cm2 measured with a Hall-bar device at 7 K illustrates the high quality of the
heterostructure thanks to the high Si0.3Ge0.7 SRB quality.
acknowledgement: The Ge project received funding from the European Union's Horizon
Europe programme under the Grant Agreement 101069515 – IGNITE. Siltronic AG is acknowledged
for providing the SRB wafers. This work was supported by Imec's Industrial Affiliation
Program on Quantum Computing.
article_number: '108231'
article_processing_charge: No
article_type: original
author:
- first_name: Yosuke
full_name: Shimura, Yosuke
last_name: Shimura
- first_name: Clement
full_name: Godfrin, Clement
last_name: Godfrin
- first_name: Andriy
full_name: Hikavyy, Andriy
last_name: Hikavyy
- first_name: Roy
full_name: Li, Roy
last_name: Li
- first_name: Juan L
full_name: Aguilera Servin, Juan L
id: 2A67C376-F248-11E8-B48F-1D18A9856A87
last_name: Aguilera Servin
orcid: 0000-0002-2862-8372
- first_name: Georgios
full_name: Katsaros, Georgios
id: 38DB5788-F248-11E8-B48F-1D18A9856A87
last_name: Katsaros
orcid: 0000-0001-8342-202X
- first_name: Paola
full_name: Favia, Paola
last_name: Favia
- first_name: Han
full_name: Han, Han
last_name: Han
- first_name: Danny
full_name: Wan, Danny
last_name: Wan
- first_name: Kristiaan
full_name: de Greve, Kristiaan
last_name: de Greve
- first_name: Roger
full_name: Loo, Roger
last_name: Loo
citation:
ama: Shimura Y, Godfrin C, Hikavyy A, et al. Compressively strained epitaxial Ge
layers for quantum computing applications. Materials Science in Semiconductor
Processing. 2024;174(5). doi:10.1016/j.mssp.2024.108231
apa: Shimura, Y., Godfrin, C., Hikavyy, A., Li, R., Aguilera Servin, J. L., Katsaros,
G., … Loo, R. (2024). Compressively strained epitaxial Ge layers for quantum computing
applications. Materials Science in Semiconductor Processing. Elsevier.
https://doi.org/10.1016/j.mssp.2024.108231
chicago: Shimura, Yosuke, Clement Godfrin, Andriy Hikavyy, Roy Li, Juan L Aguilera
Servin, Georgios Katsaros, Paola Favia, et al. “Compressively Strained Epitaxial
Ge Layers for Quantum Computing Applications.” Materials Science in Semiconductor
Processing. Elsevier, 2024. https://doi.org/10.1016/j.mssp.2024.108231.
ieee: Y. Shimura et al., “Compressively strained epitaxial Ge layers for
quantum computing applications,” Materials Science in Semiconductor Processing,
vol. 174, no. 5. Elsevier, 2024.
ista: Shimura Y, Godfrin C, Hikavyy A, Li R, Aguilera Servin JL, Katsaros G, Favia
P, Han H, Wan D, de Greve K, Loo R. 2024. Compressively strained epitaxial Ge
layers for quantum computing applications. Materials Science in Semiconductor
Processing. 174(5), 108231.
mla: Shimura, Yosuke, et al. “Compressively Strained Epitaxial Ge Layers for Quantum
Computing Applications.” Materials Science in Semiconductor Processing,
vol. 174, no. 5, 108231, Elsevier, 2024, doi:10.1016/j.mssp.2024.108231.
short: Y. Shimura, C. Godfrin, A. Hikavyy, R. Li, J.L. Aguilera Servin, G. Katsaros,
P. Favia, H. Han, D. Wan, K. de Greve, R. Loo, Materials Science in Semiconductor
Processing 174 (2024).
date_created: 2024-02-22T14:10:40Z
date_published: 2024-02-20T00:00:00Z
date_updated: 2024-02-26T10:36:35Z
day: '20'
ddc:
- '530'
department:
- _id: GeKa
- _id: NanoFab
doi: 10.1016/j.mssp.2024.108231
has_accepted_license: '1'
intvolume: ' 174'
issue: '5'
keyword:
- Mechanical Engineering
- Mechanics of Materials
- Condensed Matter Physics
- General Materials Science
language:
- iso: eng
license: https://creativecommons.org/licenses/by/4.0/
main_file_link:
- open_access: '1'
url: https://doi.org/10.1016/j.mssp.2024.108231
month: '02'
oa: 1
oa_version: Published Version
project:
- _id: 34c0acea-11ca-11ed-8bc3-8775e10fd452
grant_number: '101069515'
name: Integrated GermaNIum quanTum tEchnology
publication: Materials Science in Semiconductor Processing
publication_identifier:
issn:
- 1369-8001
publication_status: epub_ahead
publisher: Elsevier
quality_controlled: '1'
status: public
title: Compressively strained epitaxial Ge layers for quantum computing applications
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: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 174
year: '2024'
...
---
_id: '14434'
abstract:
- lang: eng
text: High entropy alloys (HEAs) are highly suitable candidate catalysts for oxygen
evolution and reduction reactions (OER/ORR) as they offer numerous parameters
for optimizing the electronic structure and catalytic sites. Herein, FeCoNiMoW
HEA nanoparticles are synthesized using a solution‐based low‐temperature approach.
Such FeCoNiMoW nanoparticles show high entropy properties, subtle lattice distortions,
and modulated electronic structure, leading to superior OER performance with an
overpotential of 233 mV at 10 mA cm−2 and 276 mV at 100 mA cm−2.
Density functional theory calculations reveal the electronic structures of the
FeCoNiMoW active sites with an optimized d‐band center position that enables suitable
adsorption of OOH* intermediates and reduces the Gibbs free energy barrier in
the OER process. Aqueous zinc–air batteries (ZABs) based on this HEA demonstrate
a high open circuit potential of 1.59 V, a peak power density of 116.9 mW cm−2,
a specific capacity of 857 mAh gZn−1,
and excellent stability for over 660 h of continuous charge–discharge cycles.
Flexible and solid ZABs are also assembled and tested, displaying excellent charge–discharge
performance at different bending angles. This work shows the significance of 4d/5d
metal‐modulated electronic structure and optimized adsorption ability to improve
the performance of OER/ORR, ZABs, and beyond.
acknowledged_ssus:
- _id: EM-Fac
acknowledgement: The authors acknowledge funding from Generalitat de Catalunya 2021
SGR 01581; the project COMBENERGY, PID2019-105490RB-C32, from the Spanish Ministerio
de Ciencia e Innovación; the National Natural Science Foundation of China (22102002);
the Anhui Provincial Natural Science Foundation (2108085QE192); Zhejiang Province
key research and development project (2023C01191); the Foundation of State Key Laboratory
of High-efficiency Utilization of Coal and Green Chemical Engineering (GrantNo.2022-K31);
and The Key Research and Development Program of Hebei Province (20314305D). IREC
is funded by the CERCA Programme from the Generalitat de Catalunya. L.L.Y. thanks
the China Scholarship Council (CSC) for the scholarship support (202008130132).
This research was supported by the Scientific Service Units (SSU) of ISTA (Institute
of Science and Technology Austria) through resources provided by the Electron Microscopy
Facility (EMF). S.L., S.H., and M.I. acknowledge funding by ISTA and the Werner
Siemens.
article_number: '2303719'
article_processing_charge: No
article_type: original
author:
- first_name: Ren
full_name: He, Ren
last_name: He
- first_name: Linlin
full_name: Yang, Linlin
last_name: Yang
- first_name: Yu
full_name: Zhang, Yu
last_name: Zhang
- first_name: Daochuan
full_name: Jiang, Daochuan
last_name: Jiang
- first_name: Seungho
full_name: Lee, Seungho
id: BB243B88-D767-11E9-B658-BC13E6697425
last_name: Lee
orcid: 0000-0002-6962-8598
- first_name: Sharona
full_name: Horta, Sharona
id: 03a7e858-01b1-11ec-8b71-99ae6c4a05bc
last_name: Horta
- first_name: Zhifu
full_name: Liang, Zhifu
last_name: Liang
- first_name: Xuan
full_name: Lu, Xuan
last_name: Lu
- first_name: Ahmad
full_name: Ostovari Moghaddam, Ahmad
last_name: Ostovari Moghaddam
- first_name: Junshan
full_name: Li, Junshan
last_name: Li
- first_name: Maria
full_name: Ibáñez, Maria
id: 43C61214-F248-11E8-B48F-1D18A9856A87
last_name: Ibáñez
orcid: 0000-0001-5013-2843
- first_name: Ying
full_name: Xu, Ying
last_name: Xu
- first_name: Yingtang
full_name: Zhou, Yingtang
last_name: Zhou
- first_name: Andreu
full_name: Cabot, Andreu
last_name: Cabot
citation:
ama: He R, Yang L, Zhang Y, et al. A 3d‐4d‐5d high entropy alloy as a bifunctional
oxygen catalyst for robust aqueous zinc–air batteries. Advanced Materials.
2023. doi:10.1002/adma.202303719
apa: He, R., Yang, L., Zhang, Y., Jiang, D., Lee, S., Horta, S., … Cabot, A. (2023).
A 3d‐4d‐5d high entropy alloy as a bifunctional oxygen catalyst for robust aqueous
zinc–air batteries. Advanced Materials. Wiley. https://doi.org/10.1002/adma.202303719
chicago: He, Ren, Linlin Yang, Yu Zhang, Daochuan Jiang, Seungho Lee, Sharona Horta,
Zhifu Liang, et al. “A 3d‐4d‐5d High Entropy Alloy as a Bifunctional Oxygen Catalyst
for Robust Aqueous Zinc–Air Batteries.” Advanced Materials. Wiley, 2023.
https://doi.org/10.1002/adma.202303719.
ieee: R. He et al., “A 3d‐4d‐5d high entropy alloy as a bifunctional oxygen
catalyst for robust aqueous zinc–air batteries,” Advanced Materials. Wiley,
2023.
ista: He R, Yang L, Zhang Y, Jiang D, Lee S, Horta S, Liang Z, Lu X, Ostovari Moghaddam
A, Li J, Ibáñez M, Xu Y, Zhou Y, Cabot A. 2023. A 3d‐4d‐5d high entropy alloy
as a bifunctional oxygen catalyst for robust aqueous zinc–air batteries. Advanced
Materials., 2303719.
mla: He, Ren, et al. “A 3d‐4d‐5d High Entropy Alloy as a Bifunctional Oxygen Catalyst
for Robust Aqueous Zinc–Air Batteries.” Advanced Materials, 2303719, Wiley,
2023, doi:10.1002/adma.202303719.
short: R. He, L. Yang, Y. Zhang, D. Jiang, S. Lee, S. Horta, Z. Liang, X. Lu, A.
Ostovari Moghaddam, J. Li, M. Ibáñez, Y. Xu, Y. Zhou, A. Cabot, Advanced Materials
(2023).
date_created: 2023-10-17T10:52:23Z
date_published: 2023-07-24T00:00:00Z
date_updated: 2023-12-13T13:03:23Z
day: '24'
department:
- _id: MaIb
doi: 10.1002/adma.202303719
external_id:
isi:
- '001083876900001'
pmid:
- '37487245'
isi: 1
keyword:
- Mechanical Engineering
- Mechanics of Materials
- General Materials Science
language:
- iso: eng
month: '07'
oa_version: None
pmid: 1
project:
- _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:
issn:
- 0935-9648
- 1521-4095
publication_status: epub_ahead
publisher: Wiley
quality_controlled: '1'
status: public
title: A 3d‐4d‐5d high entropy alloy as a bifunctional oxygen catalyst for robust
aqueous zinc–air batteries
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2023'
...
---
_id: '14435'
abstract:
- lang: eng
text: Low‐cost, safe, and environmental‐friendly rechargeable aqueous zinc‐ion batteries
(ZIBs) are promising as next‐generation energy storage devices for wearable electronics
among other applications. However, sluggish ionic transport kinetics and the unstable
electrode structure during ionic insertion/extraction hampers their deployment.
Herein, we propose a new cathode material based on a layered metal chalcogenide
(LMC), bismuth telluride (Bi2Te3), coated
with polypyrrole (PPy). Taking advantage of the PPy coating, the Bi2Te3@PPy
composite presents strong ionic absorption affinity, high oxidation resistance,
and high structural stability. The ZIBs based on Bi2Te3@PPy
cathodes exhibit high capacities and ultra‐long lifespans of over 5000 cycles.
They also present outstanding stability even under bending. In addition, we analyze
here the reaction mechanism using in situ X‐ray diffraction, X‐ray photoelectron
spectroscopy, and computational tools and demonstrate that, in the aqueous system,
Zn2+ is not inserted into the cathode as previously assumed.
In contrast, proton charge storage dominates the process. Overall, this work not
only shows the great potential of LMCs as ZIBs cathode materials and the advantages
of PPy coating, but also clarifies the charge/discharge mechanism in rechargeable
ZIBs based on LMCs.
article_number: '2305128'
article_processing_charge: No
article_type: original
author:
- first_name: Guifang
full_name: Zeng, Guifang
last_name: Zeng
- first_name: Qing
full_name: Sun, Qing
last_name: Sun
- first_name: Sharona
full_name: Horta, Sharona
id: 03a7e858-01b1-11ec-8b71-99ae6c4a05bc
last_name: Horta
- first_name: Shang
full_name: Wang, Shang
last_name: Wang
- first_name: Xuan
full_name: Lu, Xuan
last_name: Lu
- first_name: Chaoyue
full_name: Zhang, Chaoyue
last_name: Zhang
- first_name: Jing
full_name: Li, Jing
last_name: Li
- first_name: Junshan
full_name: Li, Junshan
last_name: Li
- first_name: Lijie
full_name: Ci, Lijie
last_name: Ci
- first_name: Yanhong
full_name: Tian, Yanhong
last_name: Tian
- first_name: Maria
full_name: Ibáñez, Maria
id: 43C61214-F248-11E8-B48F-1D18A9856A87
last_name: Ibáñez
orcid: 0000-0001-5013-2843
- first_name: Andreu
full_name: Cabot, Andreu
last_name: Cabot
citation:
ama: 'Zeng G, Sun Q, Horta S, et al. A layered Bi2Te3@PPy cathode for aqueous zinc
ion batteries: Mechanism and application in printed flexible batteries. Advanced
Materials. doi:10.1002/adma.202305128'
apa: 'Zeng, G., Sun, Q., Horta, S., Wang, S., Lu, X., Zhang, C., … Cabot, A. (n.d.).
A layered Bi2Te3@PPy cathode for aqueous zinc ion batteries: Mechanism and application
in printed flexible batteries. Advanced Materials. Wiley. https://doi.org/10.1002/adma.202305128'
chicago: 'Zeng, Guifang, Qing Sun, Sharona Horta, Shang Wang, Xuan Lu, Chaoyue Zhang,
Jing Li, et al. “A Layered Bi2Te3@PPy Cathode for Aqueous Zinc Ion Batteries:
Mechanism and Application in Printed Flexible Batteries.” Advanced Materials.
Wiley, n.d. https://doi.org/10.1002/adma.202305128.'
ieee: 'G. Zeng et al., “A layered Bi2Te3@PPy cathode for aqueous zinc ion
batteries: Mechanism and application in printed flexible batteries,” Advanced
Materials. Wiley.'
ista: 'Zeng G, Sun Q, Horta S, Wang S, Lu X, Zhang C, Li J, Li J, Ci L, Tian Y,
Ibáñez M, Cabot A. A layered Bi2Te3@PPy cathode for aqueous zinc ion batteries:
Mechanism and application in printed flexible batteries. Advanced Materials.,
2305128.'
mla: 'Zeng, Guifang, et al. “A Layered Bi2Te3@PPy Cathode for Aqueous Zinc Ion Batteries:
Mechanism and Application in Printed Flexible Batteries.” Advanced Materials,
2305128, Wiley, doi:10.1002/adma.202305128.'
short: G. Zeng, Q. Sun, S. Horta, S. Wang, X. Lu, C. Zhang, J. Li, J. Li, L. Ci,
Y. Tian, M. Ibáñez, A. Cabot, Advanced Materials (n.d.).
date_created: 2023-10-17T10:53:56Z
date_published: 2023-08-09T00:00:00Z
date_updated: 2023-12-13T13:03:53Z
day: '09'
department:
- _id: MaIb
doi: 10.1002/adma.202305128
external_id:
isi:
- '001085681000001'
pmid:
- '37555532'
isi: 1
keyword:
- Mechanical Engineering
- Mechanics of Materials
- General Materials Science
language:
- iso: eng
month: '08'
oa_version: None
pmid: 1
publication: Advanced Materials
publication_identifier:
eissn:
- 1521-4095
issn:
- 0935-9648
publication_status: accepted
publisher: Wiley
quality_controlled: '1'
status: public
title: 'A layered Bi2Te3@PPy cathode for aqueous zinc ion batteries: Mechanism and
application in printed flexible batteries'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2023'
...
---
_id: '13197'
abstract:
- lang: eng
text: "Nominally identical materials exchange net electric charge during contact
through a mechanism that is still debated. ‘Mosaic models’, in which surfaces
are presumed to consist of a random patchwork of microscopic donor/acceptor sites,
offer an appealing explanation for this phenomenon. However, recent experiments
have shown that global differences persist even between same-material samples,
which the standard mosaic framework does not account for. Here, we expand the
mosaic framework by incorporating global differences in the densities of donor/acceptor
sites. We develop\r\nan analytical model, backed by numerical simulations, that
smoothly connects the global and deterministic charge transfer of different materials
to the local and stochastic mosaic picture normally associated with identical
materials. Going further, we extend our model to explain the effect of contact
asymmetries during sliding, providing a plausible explanation for reversal of
charging sign that has been observed experimentally."
acknowledgement: "This project has received funding from the European Research Council
Grant Agreement No. 949120 and from\r\nthe European Union’s Horizon 2020 research
and innovation program under the Marie Sklodowska-Curie Grant\r\nAgreement No. 754411. "
article_number: '065601'
article_processing_charge: No
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: 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, Waitukaitis SR. Asymmetries in triboelectric charging: Generalizing
mosaic models to different-material samples and sliding contacts. Physical
Review Materials. 2023;7(6). doi:10.1103/physrevmaterials.7.065601'
apa: 'Grosjean, G. M., & Waitukaitis, S. R. (2023). Asymmetries in triboelectric
charging: Generalizing mosaic models to different-material samples and sliding
contacts. Physical Review Materials. American Physical Society. https://doi.org/10.1103/physrevmaterials.7.065601'
chicago: 'Grosjean, Galien M, and Scott R Waitukaitis. “Asymmetries in Triboelectric
Charging: Generalizing Mosaic Models to Different-Material Samples and Sliding
Contacts.” Physical Review Materials. American Physical Society, 2023.
https://doi.org/10.1103/physrevmaterials.7.065601.'
ieee: 'G. M. Grosjean and S. R. Waitukaitis, “Asymmetries in triboelectric charging:
Generalizing mosaic models to different-material samples and sliding contacts,”
Physical Review Materials, vol. 7, no. 6. American Physical Society, 2023.'
ista: 'Grosjean GM, Waitukaitis SR. 2023. Asymmetries in triboelectric charging:
Generalizing mosaic models to different-material samples and sliding contacts.
Physical Review Materials. 7(6), 065601.'
mla: 'Grosjean, Galien M., and Scott R. Waitukaitis. “Asymmetries in Triboelectric
Charging: Generalizing Mosaic Models to Different-Material Samples and Sliding
Contacts.” Physical Review Materials, vol. 7, no. 6, 065601, American Physical
Society, 2023, doi:10.1103/physrevmaterials.7.065601.'
short: G.M. Grosjean, S.R. Waitukaitis, Physical Review Materials 7 (2023).
date_created: 2023-07-07T12:48:01Z
date_published: 2023-06-13T00:00:00Z
date_updated: 2023-08-02T06:34:47Z
day: '13'
ddc:
- '537'
department:
- _id: ScWa
doi: 10.1103/physrevmaterials.7.065601
ec_funded: 1
external_id:
arxiv:
- '2304.12861'
isi:
- '001019565900002'
file:
- access_level: open_access
checksum: 75584730d9cdd50eeccb4c52c509776d
content_type: application/pdf
creator: ggrosjea
date_created: 2023-07-07T12:49:51Z
date_updated: 2023-07-07T12:49:51Z
file_id: '13198'
file_name: Mosaic_asymmetries.pdf
file_size: 1127040
relation: main_file
success: 1
file_date_updated: 2023-07-07T12:49:51Z
has_accepted_license: '1'
intvolume: ' 7'
isi: 1
issue: '6'
keyword:
- Physics and Astronomy (miscellaneous)
- General Materials Science
language:
- iso: eng
month: '06'
oa: 1
oa_version: Submitted Version
project:
- _id: 0aa60e99-070f-11eb-9043-a6de6bdc3afa
call_identifier: H2020
grant_number: '949120'
name: 'Tribocharge: a multi-scale approach to an enduring problem in physics'
- _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'
status: public
title: 'Asymmetries in triboelectric charging: Generalizing mosaic models to different-material
samples and sliding contacts'
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 7
year: '2023'
...
---
_id: '13251'
abstract:
- lang: eng
text: A rotating organic cation and a dynamically disordered soft inorganic cage
are the hallmark features of organic-inorganic lead-halide perovskites. Understanding
the interplay between these two subsystems is a challenging problem, but it is
this coupling that is widely conjectured to be responsible for the unique behavior
of photocarriers in these materials. In this work, we use the fact that the polarizability
of the organic cation strongly depends on the ambient electrostatic environment
to put the molecule forward as a sensitive probe of the local crystal fields inside
the lattice cell. We measure the average polarizability of the C/N–H bond stretching
mode by means of infrared spectroscopy, which allows us to deduce the character
of the motion of the cation molecule, find the magnitude of the local crystal
field, and place an estimate on the strength of the hydrogen bond between the
hydrogen and halide atoms. Our results pave the way for understanding electric
fields in lead-halide perovskites using infrared bond spectroscopy.
acknowledgement: "We thank Bingqing Cheng and Hong-Zhou Ye for valuable discussions;
Y.W.’s work at IST Austria was supported through ISTernship summer internship program
funded by OeADGmbH; D.L. and Z.A. acknowledge support by IST Austria (ISTA); M.L.
acknowledges support by the European Research Council (ERC) Starting Grant No. 801770
(ANGULON).\r\nA.A.Z. and O.M.B. acknowledge support by KAUST."
article_processing_charge: Yes (via OA deal)
article_type: original
arxiv: 1
author:
- first_name: Yujing
full_name: Wei, Yujing
id: 0c5ff007-2600-11ee-b896-98bd8d663294
last_name: Wei
orcid: 0000-0001-8913-9719
- first_name: Artem
full_name: Volosniev, Artem
id: 37D278BC-F248-11E8-B48F-1D18A9856A87
last_name: Volosniev
orcid: 0000-0003-0393-5525
- first_name: Dusan
full_name: Lorenc, Dusan
id: 40D8A3E6-F248-11E8-B48F-1D18A9856A87
last_name: Lorenc
- first_name: Ayan A.
full_name: Zhumekenov, Ayan A.
last_name: Zhumekenov
- first_name: Osman M.
full_name: Bakr, Osman M.
last_name: Bakr
- first_name: Mikhail
full_name: Lemeshko, Mikhail
id: 37CB05FA-F248-11E8-B48F-1D18A9856A87
last_name: Lemeshko
orcid: 0000-0002-6990-7802
- first_name: Zhanybek
full_name: Alpichshev, Zhanybek
id: 45E67A2A-F248-11E8-B48F-1D18A9856A87
last_name: Alpichshev
orcid: 0000-0002-7183-5203
citation:
ama: Wei Y, Volosniev A, Lorenc D, et al. Bond polarizability as a probe of local
crystal fields in hybrid lead-halide perovskites. The Journal of Physical Chemistry
Letters. 2023;14(27):6309-6314. doi:10.1021/acs.jpclett.3c01158
apa: Wei, Y., Volosniev, A., Lorenc, D., Zhumekenov, A. A., Bakr, O. M., Lemeshko,
M., & Alpichshev, Z. (2023). Bond polarizability as a probe of local crystal
fields in hybrid lead-halide perovskites. The Journal of Physical Chemistry
Letters. American Chemical Society. https://doi.org/10.1021/acs.jpclett.3c01158
chicago: Wei, Yujing, Artem Volosniev, Dusan Lorenc, Ayan A. Zhumekenov, Osman M.
Bakr, Mikhail Lemeshko, and Zhanybek Alpichshev. “Bond Polarizability as a Probe
of Local Crystal Fields in Hybrid Lead-Halide Perovskites.” The Journal of
Physical Chemistry Letters. American Chemical Society, 2023. https://doi.org/10.1021/acs.jpclett.3c01158.
ieee: Y. Wei et al., “Bond polarizability as a probe of local crystal fields
in hybrid lead-halide perovskites,” The Journal of Physical Chemistry Letters,
vol. 14, no. 27. American Chemical Society, pp. 6309–6314, 2023.
ista: Wei Y, Volosniev A, Lorenc D, Zhumekenov AA, Bakr OM, Lemeshko M, Alpichshev
Z. 2023. Bond polarizability as a probe of local crystal fields in hybrid lead-halide
perovskites. The Journal of Physical Chemistry Letters. 14(27), 6309–6314.
mla: Wei, Yujing, et al. “Bond Polarizability as a Probe of Local Crystal Fields
in Hybrid Lead-Halide Perovskites.” The Journal of Physical Chemistry Letters,
vol. 14, no. 27, American Chemical Society, 2023, pp. 6309–14, doi:10.1021/acs.jpclett.3c01158.
short: Y. Wei, A. Volosniev, D. Lorenc, A.A. Zhumekenov, O.M. Bakr, M. Lemeshko,
Z. Alpichshev, The Journal of Physical Chemistry Letters 14 (2023) 6309–6314.
date_created: 2023-07-18T11:13:17Z
date_published: 2023-07-05T00:00:00Z
date_updated: 2023-07-19T06:59:19Z
day: '05'
ddc:
- '530'
department:
- _id: MiLe
- _id: ZhAl
doi: 10.1021/acs.jpclett.3c01158
ec_funded: 1
external_id:
arxiv:
- '2304.14198'
isi:
- '001022811500001'
file:
- access_level: open_access
checksum: c0c040063f06a51b9c463adc504f1a23
content_type: application/pdf
creator: dernst
date_created: 2023-07-19T06:55:39Z
date_updated: 2023-07-19T06:55:39Z
file_id: '13253'
file_name: 2023_JourPhysChemistry_Wei.pdf
file_size: 2121252
relation: main_file
success: 1
file_date_updated: 2023-07-19T06:55:39Z
has_accepted_license: '1'
intvolume: ' 14'
isi: 1
issue: '27'
keyword:
- General Materials Science
- Physical and Theoretical Chemistry
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
page: 6309-6314
project:
- _id: 2688CF98-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '801770'
name: 'Angulon: physics and applications of a new quasiparticle'
publication: The Journal of Physical Chemistry Letters
publication_identifier:
eissn:
- 1948-7185
publication_status: published
publisher: American Chemical Society
quality_controlled: '1'
status: public
title: Bond polarizability as a probe of local crystal fields in hybrid lead-halide
perovskites
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: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 14
year: '2023'
...
---
_id: '13346'
abstract:
- lang: eng
text: The self-assembly of nanoparticles driven by small molecules or ions may produce
colloidal superlattices with features and properties reminiscent of those of metals
or semiconductors. However, to what extent the properties of such supramolecular
crystals actually resemble those of atomic materials often remains unclear. Here,
we present coarse-grained molecular simulations explicitly demonstrating how a
behavior evocative of that of semiconductors may emerge in a colloidal superlattice.
As a case study, we focus on gold nanoparticles bearing positively charged groups
that self-assemble into FCC crystals via mediation by citrate counterions. In
silico ohmic experiments show how the dynamically diverse behavior of the ions
in different superlattice domains allows the opening of conductive ionic gates
above certain levels of applied electric fields. The observed binary conductive/nonconductive
behavior is reminiscent of that of conventional semiconductors, while, at a supramolecular
level, crossing the “band gap” requires a sufficient electrostatic stimulus to
break the intermolecular interactions and make ions diffuse throughout the superlattice’s
cavities.
article_processing_charge: No
article_type: original
author:
- first_name: Chiara
full_name: Lionello, Chiara
last_name: Lionello
- first_name: Claudio
full_name: Perego, Claudio
last_name: Perego
- first_name: Andrea
full_name: Gardin, Andrea
last_name: Gardin
- first_name: Rafal
full_name: Klajn, Rafal
id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b
last_name: Klajn
- first_name: Giovanni M.
full_name: Pavan, Giovanni M.
last_name: Pavan
citation:
ama: Lionello C, Perego C, Gardin A, Klajn R, Pavan GM. Supramolecular semiconductivity
through emerging ionic gates in ion–nanoparticle superlattices. ACS Nano.
2023;17(1):275-287. doi:10.1021/acsnano.2c07558
apa: Lionello, C., Perego, C., Gardin, A., Klajn, R., & Pavan, G. M. (2023).
Supramolecular semiconductivity through emerging ionic gates in ion–nanoparticle
superlattices. ACS Nano. American Chemical Society. https://doi.org/10.1021/acsnano.2c07558
chicago: Lionello, Chiara, Claudio Perego, Andrea Gardin, Rafal Klajn, and Giovanni
M. Pavan. “Supramolecular Semiconductivity through Emerging Ionic Gates in Ion–Nanoparticle
Superlattices.” ACS Nano. American Chemical Society, 2023. https://doi.org/10.1021/acsnano.2c07558.
ieee: C. Lionello, C. Perego, A. Gardin, R. Klajn, and G. M. Pavan, “Supramolecular
semiconductivity through emerging ionic gates in ion–nanoparticle superlattices,”
ACS Nano, vol. 17, no. 1. American Chemical Society, pp. 275–287, 2023.
ista: Lionello C, Perego C, Gardin A, Klajn R, Pavan GM. 2023. Supramolecular semiconductivity
through emerging ionic gates in ion–nanoparticle superlattices. ACS Nano. 17(1),
275–287.
mla: Lionello, Chiara, et al. “Supramolecular Semiconductivity through Emerging
Ionic Gates in Ion–Nanoparticle Superlattices.” ACS Nano, vol. 17, no.
1, American Chemical Society, 2023, pp. 275–87, doi:10.1021/acsnano.2c07558.
short: C. Lionello, C. Perego, A. Gardin, R. Klajn, G.M. Pavan, ACS Nano 17 (2023)
275–287.
date_created: 2023-08-01T09:30:29Z
date_published: 2023-01-10T00:00:00Z
date_updated: 2023-08-02T06:51:15Z
day: '10'
doi: 10.1021/acsnano.2c07558
extern: '1'
intvolume: ' 17'
issue: '1'
keyword:
- General Physics and Astronomy
- General Engineering
- General Materials Science
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1021/acsnano.2c07558
month: '01'
oa: 1
oa_version: Published Version
page: 275-287
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: Supramolecular semiconductivity through emerging ionic gates in ion–nanoparticle
superlattices
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 17
year: '2023'
...
---
_id: '13988'
abstract:
- lang: eng
text: Most permissionless blockchains inherently suffer from throughput limitations.
Layer-2 systems, such as side-chains or Rollups, have been proposed as a possible
strategy to overcome this limitation. Layer-2 systems interact with the main-chain
in two ways. First, users can move funds from/to the main-chain to/from the layer-2.
Second, layer-2 systems periodically synchronize with the main-chain to keep some
form of log of their activity on the main-chain - this log is key for security.
Due to this interaction with the main-chain, which is necessary and recurrent,
layer-2 systems impose some load on the main-chain. The impact of such load on
the main-chain has been, so far, poorly understood. In addition to that, layer-2
approaches typically sacrifice decentralization and security in favor of higher
throughput. This paper presents an experimental study that analyzes the current
state of Ethereum layer-2 projects. Our goal is to assess the load they impose
on Ethereum and to understand their scalability potential in the long-run. Our
analysis shows that the impact of any given layer-2 on the main-chain is the result
of both technical aspects (how state is logged on the main-chain) and user behavior
(how often users decide to transfer funds between the layer-2 and the main-chain).
Based on our observations, we infer that without efficient mechanisms that allow
users to transfer funds in a secure and fast manner directly from one layer-2
project to another, current layer-2 systems will not be able to scale Ethereum
effectively, regardless of their technical solutions. Furthermore, from our results,
we conclude that the layer-2 systems that offer similar security guarantees as
Ethereum have limited scalability potential, while approaches that offer better
performance, sacrifice security and lead to an increase in centralization which
runs against the end-goals of permissionless blockchains.
acknowledgement: This work was supported in part by the Coordenação de Aperfeiçoamento
de Pessoal de Nivel Superior (CAPES)—Brazil (CAPES), in part by the Fundação para
a Ciência e Tecnologia (FCT) under Project UIDB/50021/2020 and Grant 2020.05270.BD,
in part by the Project COSMOS (via the Orçamento de Estado (OE) with ref. PTDC/EEI-COM/29271/2017
and via the ‘‘Programa Operacional Regional de Lisboa na sua componente Fundo Europeu
de Desenvolvimento Regional (FEDER)’’ with ref. Lisboa-01-0145-FEDER-029271), and
in part by the project Angainor with reference LISBOA-01-0145-FEDER-031456 as well
as supported by Meta Platforms for the project key Transparency at Scale.
article_processing_charge: Yes
article_type: original
author:
- first_name: Ray
full_name: Neiheiser, Ray
id: f09651b9-fec0-11ec-b5d8-934aff0e52a4
last_name: Neiheiser
orcid: 0000-0001-7227-8309
- first_name: Gustavo
full_name: Inacio, Gustavo
last_name: Inacio
- first_name: Luciana
full_name: Rech, Luciana
last_name: Rech
- first_name: Carlos
full_name: Montez, Carlos
last_name: Montez
- first_name: Miguel
full_name: Matos, Miguel
last_name: Matos
- first_name: Luis
full_name: Rodrigues, Luis
last_name: Rodrigues
citation:
ama: Neiheiser R, Inacio G, Rech L, Montez C, Matos M, Rodrigues L. Practical limitations
of Ethereum’s layer-2. IEEE Access. 2023;11:8651-8662. doi:10.1109/access.2023.3237897
apa: Neiheiser, R., Inacio, G., Rech, L., Montez, C., Matos, M., & Rodrigues,
L. (2023). Practical limitations of Ethereum’s layer-2. IEEE Access. Institute
of Electrical and Electronics Engineers. https://doi.org/10.1109/access.2023.3237897
chicago: Neiheiser, Ray, Gustavo Inacio, Luciana Rech, Carlos Montez, Miguel Matos,
and Luis Rodrigues. “Practical Limitations of Ethereum’s Layer-2.” IEEE Access.
Institute of Electrical and Electronics Engineers, 2023. https://doi.org/10.1109/access.2023.3237897.
ieee: R. Neiheiser, G. Inacio, L. Rech, C. Montez, M. Matos, and L. Rodrigues, “Practical
limitations of Ethereum’s layer-2,” IEEE Access, vol. 11. Institute of
Electrical and Electronics Engineers, pp. 8651–8662, 2023.
ista: Neiheiser R, Inacio G, Rech L, Montez C, Matos M, Rodrigues L. 2023. Practical
limitations of Ethereum’s layer-2. IEEE Access. 11, 8651–8662.
mla: Neiheiser, Ray, et al. “Practical Limitations of Ethereum’s Layer-2.” IEEE
Access, vol. 11, Institute of Electrical and Electronics Engineers, 2023,
pp. 8651–62, doi:10.1109/access.2023.3237897.
short: R. Neiheiser, G. Inacio, L. Rech, C. Montez, M. Matos, L. Rodrigues, IEEE
Access 11 (2023) 8651–8662.
date_created: 2023-08-09T12:09:57Z
date_published: 2023-08-01T00:00:00Z
date_updated: 2023-12-13T12:14:52Z
day: '01'
ddc:
- '000'
department:
- _id: ElKo
doi: 10.1109/access.2023.3237897
external_id:
isi:
- '000927831000001'
file:
- access_level: open_access
checksum: 4b80b0ff212edf7e5842fbdd53784432
content_type: application/pdf
creator: dernst
date_created: 2023-08-22T06:37:48Z
date_updated: 2023-08-22T06:37:48Z
file_id: '14166'
file_name: 2023_IEEEAccess_Neiheiser.pdf
file_size: 1289285
relation: main_file
success: 1
file_date_updated: 2023-08-22T06:37:48Z
has_accepted_license: '1'
intvolume: ' 11'
isi: 1
keyword:
- General Engineering
- General Materials Science
- General Computer Science
- Electrical and Electronic Engineering
language:
- iso: eng
month: '08'
oa: 1
oa_version: Published Version
page: 8651-8662
publication: IEEE Access
publication_identifier:
issn:
- 2169-3536
publication_status: published
publisher: Institute of Electrical and Electronics Engineers
quality_controlled: '1'
scopus_import: '1'
status: public
title: Practical limitations of Ethereum’s layer-2
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: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 11
year: '2023'
...
---
_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. Nature Nanotechnology. 2022;17(4):408-416.
doi:10.1038/s41565-022-01079-3
apa: Cai, J., Zhang, W., Xu, L., Hao, C., Ma, W., Sun, M., … Kuang, H. (2022). Polarization-sensitive
optoionic membranes from chiral plasmonic nanoparticles. Nature Nanotechnology.
Springer Nature. https://doi.org/10.1038/s41565-022-01079-3
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.” Nature Nanotechnology. Springer Nature, 2022. https://doi.org/10.1038/s41565-022-01079-3.
ieee: J. Cai et al., “Polarization-sensitive optoionic membranes from chiral
plasmonic nanoparticles,” Nature Nanotechnology, 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.” Nature Nanotechnology, vol. 17, no. 4, Springer
Nature, 2022, pp. 408–16, doi:10.1038/s41565-022-01079-3.
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: '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. Advanced
Materials. 2022;34(1). doi:10.1002/adma.202104962
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. Advanced Materials.
Wiley. https://doi.org/10.1002/adma.202104962
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.” Advanced Materials. Wiley, 2022. https://doi.org/10.1002/adma.202104962.
ieee: R. H. Huang et al., “Self‐complementary zwitterionic peptides direct
nanoparticle assembly and enable enzymatic selection of endocytic pathways,” Advanced
Materials, 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.” Advanced
Materials, vol. 34, no. 1, 2104962, Wiley, 2022, doi:10.1002/adma.202104962.
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: '12236'
abstract:
- lang: eng
text: High-entropy materials offer numerous advantages as catalysts, including a
flexible composition to tune the catalytic activity and selectivity and a large
variety of adsorption/reaction sites for multistep or multiple reactions. Herein,
we report on the synthesis, properties, and electrocatalytic performance of an
amorphous high-entropy boride based on abundant transition metals, CoFeNiMnZnB.
This metal boride provides excellent performance toward the oxygen evolution reaction
(OER), including a low overpotential of 261 mV at 10 mA cm–2, a reduced Tafel
slope of 56.8 mV dec–1, and very high stability. The outstanding OER performance
of CoFeNiMnZnB is attributed to the synergistic interactions between the different
metals, the leaching of Zn ions, the generation of oxygen vacancies, and the in
situ formation of an amorphous oxyhydroxide at the CoFeNiMnZnB surface during
the OER.
acknowledgement: This work was supported by the Spanish MCIN project COMBENERGY (PID2019-105490RB-C32).
X.W. and L.Y. thank the China Scholarship Council (CSC) for the scholarship support.
article_processing_charge: No
article_type: original
author:
- first_name: Xiang
full_name: Wang, Xiang
last_name: Wang
- first_name: Yong
full_name: Zuo, Yong
last_name: Zuo
- first_name: Sharona
full_name: Horta, Sharona
id: 03a7e858-01b1-11ec-8b71-99ae6c4a05bc
last_name: Horta
- first_name: Ren
full_name: He, Ren
last_name: He
- first_name: Linlin
full_name: Yang, Linlin
last_name: Yang
- first_name: Ahmad
full_name: Ostovari Moghaddam, Ahmad
last_name: Ostovari Moghaddam
- first_name: Maria
full_name: Ibáñez, Maria
id: 43C61214-F248-11E8-B48F-1D18A9856A87
last_name: Ibáñez
orcid: 0000-0001-5013-2843
- first_name: Xueqiang
full_name: Qi, Xueqiang
last_name: Qi
- first_name: Andreu
full_name: Cabot, Andreu
last_name: Cabot
citation:
ama: Wang X, Zuo Y, Horta S, et al. CoFeNiMnZnB as a high-entropy metal boride to
boost the oxygen evolution reaction. ACS Applied Materials & Interfaces.
2022;14(42):48212-48219. doi:10.1021/acsami.2c11627
apa: Wang, X., Zuo, Y., Horta, S., He, R., Yang, L., Ostovari Moghaddam, A., … Cabot,
A. (2022). CoFeNiMnZnB as a high-entropy metal boride to boost the oxygen evolution
reaction. ACS Applied Materials & Interfaces. American Chemical Society.
https://doi.org/10.1021/acsami.2c11627
chicago: Wang, Xiang, Yong Zuo, Sharona Horta, Ren He, Linlin Yang, Ahmad Ostovari
Moghaddam, Maria Ibáñez, Xueqiang Qi, and Andreu Cabot. “CoFeNiMnZnB as a High-Entropy
Metal Boride to Boost the Oxygen Evolution Reaction.” ACS Applied Materials
& Interfaces. American Chemical Society, 2022. https://doi.org/10.1021/acsami.2c11627.
ieee: X. Wang et al., “CoFeNiMnZnB as a high-entropy metal boride to boost
the oxygen evolution reaction,” ACS Applied Materials & Interfaces,
vol. 14, no. 42. American Chemical Society, pp. 48212–48219, 2022.
ista: Wang X, Zuo Y, Horta S, He R, Yang L, Ostovari Moghaddam A, Ibáñez M, Qi X,
Cabot A. 2022. CoFeNiMnZnB as a high-entropy metal boride to boost the oxygen
evolution reaction. ACS Applied Materials & Interfaces. 14(42), 48212–48219.
mla: Wang, Xiang, et al. “CoFeNiMnZnB as a High-Entropy Metal Boride to Boost the
Oxygen Evolution Reaction.” ACS Applied Materials & Interfaces, vol.
14, no. 42, American Chemical Society, 2022, pp. 48212–19, doi:10.1021/acsami.2c11627.
short: X. Wang, Y. Zuo, S. Horta, R. He, L. Yang, A. Ostovari Moghaddam, M. Ibáñez,
X. Qi, A. Cabot, ACS Applied Materials & Interfaces 14 (2022) 48212–48219.
date_created: 2023-01-16T09:51:10Z
date_published: 2022-10-14T00:00:00Z
date_updated: 2023-10-04T08:28:14Z
day: '14'
department:
- _id: MaIb
doi: 10.1021/acsami.2c11627
external_id:
isi:
- '000873782700001'
pmid:
- '36239982'
intvolume: ' 14'
isi: 1
issue: '42'
keyword:
- General Materials Science
language:
- iso: eng
month: '10'
oa_version: None
page: 48212-48219
pmid: 1
publication: ACS Applied Materials & Interfaces
publication_identifier:
eissn:
- 1944-8252
issn:
- 1944-8244
publication_status: published
publisher: American Chemical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: CoFeNiMnZnB as a high-entropy metal boride to boost the oxygen evolution reaction
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 14
year: '2022'
...
---
_id: '12278'
abstract:
- lang: eng
text: Mercury telluride (HgTe) thin films with a critical thickness of 6.5 nm are
predicted to possess a gapless Dirac-like band structure. We report a comprehensive
study on gated and optically doped samples by magnetooptical spectroscopy in the
THz range. The quasi-classical analysis of the cyclotron resonance allowed the
mapping of the band dispersion of Dirac charge carriers in a broad range of electron
and hole doping. A smooth transition through the charge neutrality point between
Dirac holes and electrons was observed. An additional peak coming from a second
type of holes with an almost density-independent mass of around 0.04m0 was detected
in the hole-doping range and attributed to an asymmetric spin splitting of the
Dirac cone. Spectroscopic evidence for disorder-induced band energy fluctuations
could not be detected in present cyclotron resonance experiments.
acknowledgement: "This work was supported by the Austrian Science Funds (W1243, I
3456-N27, I 5539-N).\r\nOpen Access Funding by the Austrian Science Fund (FWF)."
article_number: '2492'
article_processing_charge: Yes
article_type: original
author:
- first_name: Alexey
full_name: Shuvaev, Alexey
last_name: Shuvaev
- first_name: Uladzislau
full_name: Dziom, Uladzislau
id: 6A9A37C2-8C5C-11E9-AE53-F2FDE5697425
last_name: Dziom
orcid: 0000-0002-1648-0999
- first_name: Jan
full_name: Gospodarič, Jan
last_name: Gospodarič
- first_name: Elena G.
full_name: Novik, Elena G.
last_name: Novik
- first_name: Alena A.
full_name: Dobretsova, Alena A.
last_name: Dobretsova
- first_name: Nikolay N.
full_name: Mikhailov, Nikolay N.
last_name: Mikhailov
- first_name: Ze Don
full_name: Kvon, Ze Don
last_name: Kvon
- first_name: Andrei
full_name: Pimenov, Andrei
last_name: Pimenov
citation:
ama: Shuvaev A, Dziom U, Gospodarič J, et al. Band structure near the Dirac Point
in HgTe quantum wells with critical thickness. Nanomaterials. 2022;12(14).
doi:10.3390/nano12142492
apa: Shuvaev, A., Dziom, U., Gospodarič, J., Novik, E. G., Dobretsova, A. A., Mikhailov,
N. N., … Pimenov, A. (2022). Band structure near the Dirac Point in HgTe quantum
wells with critical thickness. Nanomaterials. MDPI. https://doi.org/10.3390/nano12142492
chicago: Shuvaev, Alexey, Uladzislau Dziom, Jan Gospodarič, Elena G. Novik, Alena
A. Dobretsova, Nikolay N. Mikhailov, Ze Don Kvon, and Andrei Pimenov. “Band Structure
near the Dirac Point in HgTe Quantum Wells with Critical Thickness.” Nanomaterials.
MDPI, 2022. https://doi.org/10.3390/nano12142492.
ieee: A. Shuvaev et al., “Band structure near the Dirac Point in HgTe quantum
wells with critical thickness,” Nanomaterials, vol. 12, no. 14. MDPI, 2022.
ista: Shuvaev A, Dziom U, Gospodarič J, Novik EG, Dobretsova AA, Mikhailov NN, Kvon
ZD, Pimenov A. 2022. Band structure near the Dirac Point in HgTe quantum wells
with critical thickness. Nanomaterials. 12(14), 2492.
mla: Shuvaev, Alexey, et al. “Band Structure near the Dirac Point in HgTe Quantum
Wells with Critical Thickness.” Nanomaterials, vol. 12, no. 14, 2492, MDPI,
2022, doi:10.3390/nano12142492.
short: A. Shuvaev, U. Dziom, J. Gospodarič, E.G. Novik, A.A. Dobretsova, N.N. Mikhailov,
Z.D. Kvon, A. Pimenov, Nanomaterials 12 (2022).
date_created: 2023-01-16T10:02:31Z
date_published: 2022-07-20T00:00:00Z
date_updated: 2023-10-17T11:41:28Z
day: '20'
ddc:
- '530'
department:
- _id: ZhAl
doi: 10.3390/nano12142492
external_id:
isi:
- '000834401600001'
file:
- access_level: open_access
checksum: efad6742f89f39a18bec63116dd689a0
content_type: application/pdf
creator: dernst
date_created: 2023-01-30T11:16:54Z
date_updated: 2023-01-30T11:16:54Z
file_id: '12459'
file_name: 2022_Nanomaterials_Shuvaev.pdf
file_size: 464840
relation: main_file
success: 1
file_date_updated: 2023-01-30T11:16:54Z
has_accepted_license: '1'
intvolume: ' 12'
isi: 1
issue: '14'
keyword:
- General Materials Science
- General Chemical Engineering
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
publication: Nanomaterials
publication_identifier:
issn:
- 2079-4991
publication_status: published
publisher: MDPI
quality_controlled: '1'
scopus_import: '1'
status: public
title: Band structure near the Dirac Point in HgTe quantum wells with critical thickness
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: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 12
year: '2022'
...
---
_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. Nanomaterials. 2021;11(7). doi:10.3390/nano11071827
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.
Nanomaterials. MDPI. https://doi.org/10.3390/nano11071827
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.” Nanomaterials. MDPI, 2021. https://doi.org/10.3390/nano11071827.
ieee: M. Li et al., “Enhanced thermoelectric performance of n-type Bi2Se3
nanosheets through Sn doping,” Nanomaterials, 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.” Nanomaterials, vol. 11, no. 7, 1827, MDPI, 2021, doi:10.3390/nano11071827.
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: '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. Nano Letters. 2021;21(21):8970-8978. doi:10.1021/acs.nanolett.1c02145
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. Nano
Letters. American Chemical Society. https://doi.org/10.1021/acs.nanolett.1c02145
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.” Nano Letters. American Chemical
Society, 2021. https://doi.org/10.1021/acs.nanolett.1c02145.
ieee: D. R. Baykusheva et al., “All-optical probe of three-dimensional topological
insulators based on high-harmonic generation by circularly polarized laser fields,”
Nano Letters, 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.” Nano Letters, vol. 21, no. 21, American Chemical Society,
2021, pp. 8970–78, doi:10.1021/acs.nanolett.1c02145.
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: '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. ACS Nano. 2021;15(3):4967–4978.
doi:10.1021/acsnano.0c09866
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. ACS Nano. American Chemical Society . https://doi.org/10.1021/acsnano.0c09866
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.” ACS Nano. American Chemical Society , 2021.
https://doi.org/10.1021/acsnano.0c09866.
ieee: M. Li et al., “Effect of the annealing atmosphere on crystal phase
and thermoelectric properties of copper sulfide,” ACS Nano, 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.” ACS Nano, vol. 15, no. 3,
American Chemical Society , 2021, pp. 4967–4978, doi:10.1021/acsnano.0c09866.
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. 2D Materials. 2021;8(3). doi:10.1088/2053-1583/abeed3
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. 2D Materials. IOP Publishing. https://doi.org/10.1088/2053-1583/abeed3
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.” 2D Materials. IOP Publishing,
2021. https://doi.org/10.1088/2053-1583/abeed3.
ieee: M. Nauman et al., “Complete mapping of magnetic anisotropy for prototype
Ising van der Waals FePS3,” 2D Materials, 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.” 2D Materials, vol. 8, no. 3, 035011, IOP Publishing,
2021, doi:10.1088/2053-1583/abeed3.
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: '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. Advanced Materials.
2021;33(52). doi:10.1002/adma.202106858'
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. Advanced Materials. Wiley. https://doi.org/10.1002/adma.202106858'
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.” Advanced Materials. Wiley,
2021. https://doi.org/10.1002/adma.202106858.'
ieee: 'Y. Liu et al., “The importance of surface adsorbates in solution‐processed
thermoelectric materials: The case of SnSe,” Advanced Materials, 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.” Advanced Materials, vol. 33,
no. 52, 2106858, Wiley, 2021, doi:10.1002/adma.202106858.'
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: '10866'
abstract:
- lang: eng
text: Recent discoveries have shown that, when two layers of van der Waals (vdW)
materials are superimposed with a relative twist angle between them, the electronic
properties of the coupled system can be dramatically altered. Here, we demonstrate
that a similar concept can be extended to the optics realm, particularly to propagating
phonon polaritons–hybrid light-matter interactions. To do this, we fabricate stacks
composed of two twisted slabs of a vdW crystal (α-MoO3) supporting anisotropic
phonon polaritons (PhPs), and image the propagation of the latter when launched
by localized sources. Our images reveal that, under a critical angle, the PhPs
isofrequency curve undergoes a topological transition, in which the propagation
of PhPs is strongly guided (canalization regime) along predetermined directions
without geometric spreading. These results demonstrate a new degree of freedom
(twist angle) for controlling the propagation of polaritons at the nanoscale with
potential for nanoimaging, (bio)-sensing, or heat management.
acknowledgement: "J.T.-G. and G.Á.-P. acknowledge support through the Severo Ochoa
Program from the\r\nGovernment of the Principality of Asturias (nos. PA-18-PF-BP17-126
and PA20-PF-BP19-053,\r\nrespectively). J. M-S acknowledges financial support through
the Ramón y Cajal Program from\r\nthe Government of Spain (RYC2018-026196-I). A.Y.N.
acknowledges the Spanish Ministry of\r\nScience, Innovation and Universities (national
project no. MAT201788358-C3-3-R). P.A.-G.\r\nacknowledges support from the European
Research Council under starting grant no. 715496,\r\n2DNANOPTICA."
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Jiahua
full_name: Duan, Jiahua
last_name: Duan
- first_name: Nathaniel
full_name: Capote-Robayna, Nathaniel
last_name: Capote-Robayna
- first_name: Javier
full_name: Taboada-Gutiérrez, Javier
last_name: Taboada-Gutiérrez
- first_name: Gonzalo
full_name: Álvarez-Pérez, Gonzalo
last_name: Álvarez-Pérez
- first_name: Ivan
full_name: Prieto Gonzalez, Ivan
id: 2A307FE2-F248-11E8-B48F-1D18A9856A87
last_name: Prieto Gonzalez
orcid: 0000-0002-7370-5357
- first_name: Javier
full_name: Martín-Sánchez, Javier
last_name: Martín-Sánchez
- first_name: Alexey Y.
full_name: Nikitin, Alexey Y.
last_name: Nikitin
- first_name: Pablo
full_name: Alonso-González, Pablo
last_name: Alonso-González
citation:
ama: 'Duan J, Capote-Robayna N, Taboada-Gutiérrez J, et al. Twisted nano-optics:
Manipulating light at the nanoscale with twisted phonon polaritonic slabs. Nano
Letters. 2020;20(7):5323-5329. doi:10.1021/acs.nanolett.0c01673'
apa: 'Duan, J., Capote-Robayna, N., Taboada-Gutiérrez, J., Álvarez-Pérez, G., Prieto
Gonzalez, I., Martín-Sánchez, J., … Alonso-González, P. (2020). Twisted nano-optics:
Manipulating light at the nanoscale with twisted phonon polaritonic slabs. Nano
Letters. American Chemical Society. https://doi.org/10.1021/acs.nanolett.0c01673'
chicago: 'Duan, Jiahua, Nathaniel Capote-Robayna, Javier Taboada-Gutiérrez, Gonzalo
Álvarez-Pérez, Ivan Prieto Gonzalez, Javier Martín-Sánchez, Alexey Y. Nikitin,
and Pablo Alonso-González. “Twisted Nano-Optics: Manipulating Light at the Nanoscale
with Twisted Phonon Polaritonic Slabs.” Nano Letters. American Chemical
Society, 2020. https://doi.org/10.1021/acs.nanolett.0c01673.'
ieee: 'J. Duan et al., “Twisted nano-optics: Manipulating light at the nanoscale
with twisted phonon polaritonic slabs,” Nano Letters, vol. 20, no. 7. American
Chemical Society, pp. 5323–5329, 2020.'
ista: 'Duan J, Capote-Robayna N, Taboada-Gutiérrez J, Álvarez-Pérez G, Prieto Gonzalez
I, Martín-Sánchez J, Nikitin AY, Alonso-González P. 2020. Twisted nano-optics:
Manipulating light at the nanoscale with twisted phonon polaritonic slabs. Nano
Letters. 20(7), 5323–5329.'
mla: 'Duan, Jiahua, et al. “Twisted Nano-Optics: Manipulating Light at the Nanoscale
with Twisted Phonon Polaritonic Slabs.” Nano Letters, vol. 20, no. 7, American
Chemical Society, 2020, pp. 5323–29, doi:10.1021/acs.nanolett.0c01673.'
short: J. Duan, N. Capote-Robayna, J. Taboada-Gutiérrez, G. Álvarez-Pérez, I. Prieto
Gonzalez, J. Martín-Sánchez, A.Y. Nikitin, P. Alonso-González, Nano Letters 20
(2020) 5323–5329.
date_created: 2022-03-18T11:37:38Z
date_published: 2020-07-01T00:00:00Z
date_updated: 2023-09-05T12:05:58Z
day: '01'
department:
- _id: NanoFab
doi: 10.1021/acs.nanolett.0c01673
external_id:
arxiv:
- '2004.14599'
isi:
- '000548893200082'
pmid:
- '32530634'
intvolume: ' 20'
isi: 1
issue: '7'
keyword:
- Mechanical Engineering
- Condensed Matter Physics
- General Materials Science
- General Chemistry
- Bioengineering
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/2004.14599
month: '07'
oa: 1
oa_version: Preprint
page: 5323-5329
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: 'Twisted nano-optics: Manipulating light at the nanoscale with twisted phonon
polaritonic slabs'
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 20
year: '2020'
...
---
_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. Advanced Science. 2020;7(21). doi:10.1002/advs.202001724
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. Advanced Science.
Wiley. https://doi.org/10.1002/advs.202001724
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.”
Advanced Science. Wiley, 2020. https://doi.org/10.1002/advs.202001724.
ieee: A. Tian et al., “Oncogenic state and cell identity combinatorially
dictate the susceptibility of cells within glioma development hierarchy to IGF1R
targeting,” Advanced Science, 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.”
Advanced Science, vol. 7, no. 21, 2001724, Wiley, 2020, doi:10.1002/advs.202001724.
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: '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. Small. 2020;16(37). doi:10.1002/smll.202002135
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. Small. Wiley. https://doi.org/10.1002/smll.202002135
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.” Small. Wiley, 2020.
https://doi.org/10.1002/smll.202002135.
ieee: S. Moreno et al., “Light‐driven proton transfer for cyclic and temporal
switching of enzymatic nanoreactors,” Small, 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.” Small, vol. 16, no. 37, 2002135,
Wiley, 2020, doi:10.1002/smll.202002135.
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'
...
---
_id: '13367'
abstract:
- lang: eng
text: Confining molecules can fundamentally change their chemical and physical properties.
Confinement effects are considered instrumental at various stages of the origins
of life, and life continues to rely on layers of compartmentalization to maintain
an out-of-equilibrium state and efficiently synthesize complex biomolecules under
mild conditions. As interest in synthetic confined systems grows, we are realizing
that the principles governing reactivity under confinement are the same in abiological
systems as they are in nature. In this Review, we categorize the ways in which
nanoconfinement effects impact chemical reactivity in synthetic systems. Under
nanoconfinement, chemical properties can be modulated to increase reaction rates,
enhance selectivity and stabilize reactive species. Confinement effects also lead
to changes in physical properties. The fluorescence of light emitters, the colours
of dyes and electronic communication between electroactive species can all be
tuned under confinement. Within each of these categories, we elucidate design
principles and strategies that are widely applicable across a range of confined
systems, specifically highlighting examples of different nanocompartments that
influence reactivity in similar ways.
article_processing_charge: No
article_type: original
author:
- first_name: Angela B.
full_name: Grommet, Angela B.
last_name: Grommet
- first_name: Moran
full_name: Feller, Moran
last_name: Feller
- first_name: Rafal
full_name: Klajn, Rafal
id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b
last_name: Klajn
citation:
ama: Grommet AB, Feller M, Klajn R. Chemical reactivity under nanoconfinement. Nature
Nanotechnology. 2020;15:256-271. doi:10.1038/s41565-020-0652-2
apa: Grommet, A. B., Feller, M., & Klajn, R. (2020). Chemical reactivity under
nanoconfinement. Nature Nanotechnology. Springer Nature. https://doi.org/10.1038/s41565-020-0652-2
chicago: Grommet, Angela B., Moran Feller, and Rafal Klajn. “Chemical Reactivity
under Nanoconfinement.” Nature Nanotechnology. Springer Nature, 2020. https://doi.org/10.1038/s41565-020-0652-2.
ieee: A. B. Grommet, M. Feller, and R. Klajn, “Chemical reactivity under nanoconfinement,”
Nature Nanotechnology, vol. 15. Springer Nature, pp. 256–271, 2020.
ista: Grommet AB, Feller M, Klajn R. 2020. Chemical reactivity under nanoconfinement.
Nature Nanotechnology. 15, 256–271.
mla: Grommet, Angela B., et al. “Chemical Reactivity under Nanoconfinement.” Nature
Nanotechnology, vol. 15, Springer Nature, 2020, pp. 256–71, doi:10.1038/s41565-020-0652-2.
short: A.B. Grommet, M. Feller, R. Klajn, Nature Nanotechnology 15 (2020) 256–271.
date_created: 2023-08-01T09:37:39Z
date_published: 2020-04-17T00:00:00Z
date_updated: 2023-08-07T10:29:06Z
day: '17'
doi: 10.1038/s41565-020-0652-2
extern: '1'
external_id:
pmid:
- '32303705'
intvolume: ' 15'
keyword:
- Electrical and Electronic Engineering
- Condensed Matter Physics
- General Materials Science
- Biomedical Engineering
- Atomic and Molecular Physics
- and Optics
- Bioengineering
language:
- iso: eng
month: '04'
oa_version: None
page: 256-271
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: Chemical reactivity under nanoconfinement
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 15
year: '2020'
...