---
_id: '12331'
abstract:
- lang: eng
  text: High carrier mobility is critical to improving thermoelectric performance
    over a broad temperature range. However, traditional doping inevitably deteriorates
    carrier mobility. Herein, we develop a strategy for fine tuning of defects to
    improve carrier mobility. To begin, n-type PbTe is created by compensating for
    the intrinsic Pb vacancy in bare PbTe. Excess Pb2+ reduces vacancy scattering,
    resulting in a high carrier mobility of ∼3400 cm2 V–1 s–1. Then, excess Ag is
    introduced to compensate for the remaining intrinsic Pb vacancies. We find that
    excess Ag exhibits a dynamic doping process with increasing temperatures, increasing
    both the carrier concentration and carrier mobility throughout a wide temperature
    range; specifically, an ultrahigh carrier mobility ∼7300 cm2 V–1 s–1 is obtained
    for Pb1.01Te + 0.002Ag at 300 K. Moreover, the dynamic doping-induced high carrier
    concentration suppresses the bipolar thermal conductivity at high temperatures.
    The final step is using iodine to optimize the carrier concentration to ∼1019
    cm–3. Ultimately, a maximum ZT value of ∼1.5 and a large average ZTave value of
    ∼1.0 at 300–773 K are obtained for Pb1.01Te0.998I0.002 + 0.002Ag. These findings
    demonstrate that fine tuning of defects with <0.5% impurities can remarkably enhance
    carrier mobility and improve thermoelectric performance.
acknowledgement: The National Key Research and Development Program of China (2018YFA0702100),
  the Basic Science Center Project of the National Natural Science Foundation of China
  (51788104), the National Natural Science Foundation of China (51571007 and 51772012),
  the Beijing Natural Science Foundation (JQ18004), the 111 Project (B17002), the
  National Science Fund for Distinguished Young Scholars (51925101), and the FWF “Lise
  Meitner Fellowship” (grant agreement M2889-N). Open Access is funded by the Austrian
  Science Fund (FWF).
article_processing_charge: No
article_type: original
author:
- first_name: Siqi
  full_name: Wang, Siqi
  last_name: Wang
- first_name: Cheng
  full_name: Chang, Cheng
  id: 9E331C2E-9F27-11E9-AE48-5033E6697425
  last_name: Chang
  orcid: 0000-0002-9515-4277
- first_name: Shulin
  full_name: Bai, Shulin
  last_name: Bai
- first_name: Bingchao
  full_name: Qin, Bingchao
  last_name: Qin
- first_name: Yingcai
  full_name: Zhu, Yingcai
  last_name: Zhu
- first_name: Shaoping
  full_name: Zhan, Shaoping
  last_name: Zhan
- first_name: Junqing
  full_name: Zheng, Junqing
  last_name: Zheng
- first_name: Shuwei
  full_name: Tang, Shuwei
  last_name: Tang
- first_name: Li Dong
  full_name: Zhao, Li Dong
  last_name: Zhao
citation:
  ama: Wang S, Chang C, Bai S, et al. Fine tuning of defects enables high carrier
    mobility and enhanced thermoelectric performance of n-type PbTe. <i>Chemistry
    of Materials</i>. 2023;35(2):755-763. doi:<a href="https://doi.org/10.1021/acs.chemmater.2c03542">10.1021/acs.chemmater.2c03542</a>
  apa: Wang, S., Chang, C., Bai, S., Qin, B., Zhu, Y., Zhan, S., … Zhao, L. D. (2023).
    Fine tuning of defects enables high carrier mobility and enhanced thermoelectric
    performance of n-type PbTe. <i>Chemistry of Materials</i>. American Chemical Society.
    <a href="https://doi.org/10.1021/acs.chemmater.2c03542">https://doi.org/10.1021/acs.chemmater.2c03542</a>
  chicago: Wang, Siqi, Cheng Chang, Shulin Bai, Bingchao Qin, Yingcai Zhu, Shaoping
    Zhan, Junqing Zheng, Shuwei Tang, and Li Dong Zhao. “Fine Tuning of Defects Enables
    High Carrier Mobility and Enhanced Thermoelectric Performance of N-Type PbTe.”
    <i>Chemistry of Materials</i>. American Chemical Society, 2023. <a href="https://doi.org/10.1021/acs.chemmater.2c03542">https://doi.org/10.1021/acs.chemmater.2c03542</a>.
  ieee: S. Wang <i>et al.</i>, “Fine tuning of defects enables high carrier mobility
    and enhanced thermoelectric performance of n-type PbTe,” <i>Chemistry of Materials</i>,
    vol. 35, no. 2. American Chemical Society, pp. 755–763, 2023.
  ista: Wang S, Chang C, Bai S, Qin B, Zhu Y, Zhan S, Zheng J, Tang S, Zhao LD. 2023.
    Fine tuning of defects enables high carrier mobility and enhanced thermoelectric
    performance of n-type PbTe. Chemistry of Materials. 35(2), 755–763.
  mla: Wang, Siqi, et al. “Fine Tuning of Defects Enables High Carrier Mobility and
    Enhanced Thermoelectric Performance of N-Type PbTe.” <i>Chemistry of Materials</i>,
    vol. 35, no. 2, American Chemical Society, 2023, pp. 755–63, doi:<a href="https://doi.org/10.1021/acs.chemmater.2c03542">10.1021/acs.chemmater.2c03542</a>.
  short: S. Wang, C. Chang, S. Bai, B. Qin, Y. Zhu, S. Zhan, J. Zheng, S. Tang, L.D.
    Zhao, Chemistry of Materials 35 (2023) 755–763.
date_created: 2023-01-22T23:00:55Z
date_published: 2023-01-24T00:00:00Z
date_updated: 2023-08-14T12:57:44Z
day: '24'
ddc:
- '540'
department:
- _id: MaIb
doi: 10.1021/acs.chemmater.2c03542
external_id:
  isi:
  - '000914749700001'
file:
- access_level: open_access
  checksum: b21dca2aa7a80c068bc256bdd1fea9df
  content_type: application/pdf
  creator: dernst
  date_created: 2023-08-14T12:57:25Z
  date_updated: 2023-08-14T12:57:25Z
  file_id: '14055'
  file_name: 2023_ChemistryMaterials_Wang.pdf
  file_size: 2961043
  relation: main_file
  success: 1
file_date_updated: 2023-08-14T12:57:25Z
has_accepted_license: '1'
intvolume: '        35'
isi: 1
issue: '2'
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
page: 755-763
project:
- _id: 9B8804FC-BA93-11EA-9121-9846C619BF3A
  grant_number: M02889
  name: Bottom-up Engineering for Thermoelectric Applications
publication: Chemistry of Materials
publication_identifier:
  eissn:
  - 1520-5002
  issn:
  - 0897-4756
publication_status: published
publisher: American Chemical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: Fine tuning of defects enables high carrier mobility and enhanced thermoelectric
  performance of n-type PbTe
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: 35
year: '2023'
...
---
_id: '12237'
abstract:
- lang: eng
  text: Thermoelectric technology requires synthesizing complex materials where not
    only the crystal structure but also other structural features such as defects,
    grain size and orientation, and interfaces must be controlled. To date, conventional
    solid-state techniques are unable to provide this level of control. Herein, we
    present a synthetic approach in which dense inorganic thermoelectric materials
    are produced by the consolidation of well-defined nanoparticle powders. The idea
    is that controlling the characteristics of the powder allows the chemical transformations
    that take place during consolidation to be guided, ultimately yielding inorganic
    solids with targeted features. Different from conventional methods, syntheses
    in solution can produce particles with unprecedented control over their size,
    shape, crystal structure, composition, and surface chemistry. However, to date,
    most works have focused only on the low-cost benefits of this strategy. In this
    perspective, we first cover the opportunities that solution processing of the
    powder offers, emphasizing the potential structural features that can be controlled
    by precisely engineering the inorganic core of the particle, the surface, and
    the organization of the particles before consolidation. We then discuss the challenges
    of this synthetic approach and more practical matters related to solution processing.
    Finally, we suggest some good practices for adequate knowledge transfer and improving
    reproducibility among different laboratories.
acknowledgement: This work was financially supported by ISTA and the Werner Siemens
  Foundation. 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.
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Christine
  full_name: Fiedler, Christine
  id: bd3fceba-dc74-11ea-a0a7-c17f71817366
  last_name: Fiedler
- first_name: Tobias
  full_name: Kleinhanns, Tobias
  id: 8BD9DE16-AB3C-11E9-9C8C-2A03E6697425
  last_name: Kleinhanns
- first_name: Maria
  full_name: Garcia, Maria
  id: 6e5c50b8-97dc-11ed-be98-b0a74c84cae0
  last_name: Garcia
- first_name: Seungho
  full_name: Lee, Seungho
  id: BB243B88-D767-11E9-B658-BC13E6697425
  last_name: Lee
  orcid: 0000-0002-6962-8598
- first_name: Mariano
  full_name: Calcabrini, Mariano
  id: 45D7531A-F248-11E8-B48F-1D18A9856A87
  last_name: Calcabrini
- first_name: Maria
  full_name: Ibáñez, Maria
  id: 43C61214-F248-11E8-B48F-1D18A9856A87
  last_name: Ibáñez
  orcid: 0000-0001-5013-2843
citation:
  ama: 'Fiedler C, Kleinhanns T, Garcia M, Lee S, Calcabrini M, Ibáñez M. Solution-processed
    inorganic thermoelectric materials: Opportunities and challenges. <i>Chemistry
    of Materials</i>. 2022;34(19):8471-8489. doi:<a href="https://doi.org/10.1021/acs.chemmater.2c01967">10.1021/acs.chemmater.2c01967</a>'
  apa: 'Fiedler, C., Kleinhanns, T., Garcia, M., Lee, S., Calcabrini, M., &#38; Ibáñez,
    M. (2022). Solution-processed inorganic thermoelectric materials: Opportunities
    and challenges. <i>Chemistry of Materials</i>. American Chemical Society. <a href="https://doi.org/10.1021/acs.chemmater.2c01967">https://doi.org/10.1021/acs.chemmater.2c01967</a>'
  chicago: 'Fiedler, Christine, Tobias Kleinhanns, Maria Garcia, Seungho Lee, Mariano
    Calcabrini, and Maria Ibáñez. “Solution-Processed Inorganic Thermoelectric Materials:
    Opportunities and Challenges.” <i>Chemistry of Materials</i>. American Chemical
    Society, 2022. <a href="https://doi.org/10.1021/acs.chemmater.2c01967">https://doi.org/10.1021/acs.chemmater.2c01967</a>.'
  ieee: 'C. Fiedler, T. Kleinhanns, M. Garcia, S. Lee, M. Calcabrini, and M. Ibáñez,
    “Solution-processed inorganic thermoelectric materials: Opportunities and challenges,”
    <i>Chemistry of Materials</i>, vol. 34, no. 19. American Chemical Society, pp.
    8471–8489, 2022.'
  ista: 'Fiedler C, Kleinhanns T, Garcia M, Lee S, Calcabrini M, Ibáñez M. 2022. Solution-processed
    inorganic thermoelectric materials: Opportunities and challenges. Chemistry of
    Materials. 34(19), 8471–8489.'
  mla: 'Fiedler, Christine, et al. “Solution-Processed Inorganic Thermoelectric Materials:
    Opportunities and Challenges.” <i>Chemistry of Materials</i>, vol. 34, no. 19,
    American Chemical Society, 2022, pp. 8471–89, doi:<a href="https://doi.org/10.1021/acs.chemmater.2c01967">10.1021/acs.chemmater.2c01967</a>.'
  short: C. Fiedler, T. Kleinhanns, M. Garcia, S. Lee, M. Calcabrini, M. Ibáñez, Chemistry
    of Materials 34 (2022) 8471–8489.
date_created: 2023-01-16T09:51:26Z
date_published: 2022-09-20T00:00:00Z
date_updated: 2023-08-04T09:38:26Z
day: '20'
ddc:
- '540'
department:
- _id: MaIb
doi: 10.1021/acs.chemmater.2c01967
ec_funded: 1
external_id:
  isi:
  - '000917837600001'
  pmid:
  - '36248227'
file:
- access_level: open_access
  checksum: f7143e44ab510519d1949099c3558532
  content_type: application/pdf
  creator: dernst
  date_created: 2023-01-30T07:35:09Z
  date_updated: 2023-01-30T07:35:09Z
  file_id: '12434'
  file_name: 2022_ChemistryMaterials_Fiedler.pdf
  file_size: 10923495
  relation: main_file
  success: 1
file_date_updated: 2023-01-30T07:35:09Z
has_accepted_license: '1'
intvolume: '        34'
isi: 1
issue: '19'
keyword:
- Materials Chemistry
- General Chemical Engineering
- General Chemistry
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
page: 8471-8489
pmid: 1
project:
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '665385'
  name: International IST Doctoral Program
publication: Chemistry of Materials
publication_identifier:
  eissn:
  - 1520-5002
  issn:
  - 0897-4756
publication_status: published
publisher: American Chemical Society
quality_controlled: '1'
related_material:
  record:
  - id: '12885'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: 'Solution-processed inorganic thermoelectric materials: Opportunities and challenges'
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: 34
year: '2022'
...
---
_id: '7286'
abstract:
- lang: eng
  text: The solid electrolyte interphase (SEI) in Li and Na ion batteries forms when
    highly reducing or oxidizing electrode materials come into contact with a liquid
    organic electrolyte. Its ability to form a mechanically robust, ion-conducting,
    and electron-insulating layer critically determines performance, cycle life, and
    safety. Li or Na alkyl carbonates (LiAC and NaAC, respectively) are lead SEI components
    in state-of-the-art carbonate based electrolytes, and our fundamental understanding
    of their charge transport and mechanical properties may hold the key to designing
    electrolytes forming an improved SEI. We synthesized a homologous series of LiACs
    and NaACs from methyl to octyl analogues and characterized them with respect to
    structure, ionic conductivity, and stiffness. The compounds assume layered structures
    except for the lithium methyl carbonate. Room-temperature conductivities were
    found to be ∼10–9 S cm–1 for lithium methyl carbonate, <10–12 S cm–1 for the other
    LiACs, and <10–12 S cm–1 for the NaACs with ion transport mostly attributed to
    grain boundaries. While LiACs show stiffnesses of ∼1 GPa, NaACs become significantly
    softer with increasing chain lengths. These findings will help to more precisely
    interpret the complex results from charge transport and mechanical characterization
    of real SEIs and can give a rationale for influencing the SEI’s mechanical properties
    via the electrolyte.
article_processing_charge: No
article_type: original
author:
- first_name: Lukas
  full_name: Schafzahl, Lukas
  last_name: Schafzahl
- first_name: Heike
  full_name: Ehmann, Heike
  last_name: Ehmann
- first_name: Manfred
  full_name: Kriechbaum, Manfred
  last_name: Kriechbaum
- first_name: Jürgen
  full_name: Sattelkow, Jürgen
  last_name: Sattelkow
- first_name: Thomas
  full_name: Ganner, Thomas
  last_name: Ganner
- first_name: Harald
  full_name: Plank, Harald
  last_name: Plank
- first_name: Martin
  full_name: Wilkening, Martin
  last_name: Wilkening
- first_name: Stefan Alexander
  full_name: Freunberger, Stefan Alexander
  id: A8CA28E6-CE23-11E9-AD2D-EC27E6697425
  last_name: Freunberger
  orcid: 0000-0003-2902-5319
citation:
  ama: 'Schafzahl L, Ehmann H, Kriechbaum M, et al. Long-chain Li and Na alkyl carbonates
    as solid electrolyte interphase components: Structure, ion transport, and mechanical
    properties. <i>Chemistry of Materials</i>. 2018;30(10):3338-3345. doi:<a href="https://doi.org/10.1021/acs.chemmater.8b00750">10.1021/acs.chemmater.8b00750</a>'
  apa: 'Schafzahl, L., Ehmann, H., Kriechbaum, M., Sattelkow, J., Ganner, T., Plank,
    H., … Freunberger, S. A. (2018). Long-chain Li and Na alkyl carbonates as solid
    electrolyte interphase components: Structure, ion transport, and mechanical properties.
    <i>Chemistry of Materials</i>. ACS. <a href="https://doi.org/10.1021/acs.chemmater.8b00750">https://doi.org/10.1021/acs.chemmater.8b00750</a>'
  chicago: 'Schafzahl, Lukas, Heike Ehmann, Manfred Kriechbaum, Jürgen Sattelkow,
    Thomas Ganner, Harald Plank, Martin Wilkening, and Stefan Alexander Freunberger.
    “Long-Chain Li and Na Alkyl Carbonates as Solid Electrolyte Interphase Components:
    Structure, Ion Transport, and Mechanical Properties.” <i>Chemistry of Materials</i>.
    ACS, 2018. <a href="https://doi.org/10.1021/acs.chemmater.8b00750">https://doi.org/10.1021/acs.chemmater.8b00750</a>.'
  ieee: 'L. Schafzahl <i>et al.</i>, “Long-chain Li and Na alkyl carbonates as solid
    electrolyte interphase components: Structure, ion transport, and mechanical properties,”
    <i>Chemistry of Materials</i>, vol. 30, no. 10. ACS, pp. 3338–3345, 2018.'
  ista: 'Schafzahl L, Ehmann H, Kriechbaum M, Sattelkow J, Ganner T, Plank H, Wilkening
    M, Freunberger SA. 2018. Long-chain Li and Na alkyl carbonates as solid electrolyte
    interphase components: Structure, ion transport, and mechanical properties. Chemistry
    of Materials. 30(10), 3338–3345.'
  mla: 'Schafzahl, Lukas, et al. “Long-Chain Li and Na Alkyl Carbonates as Solid Electrolyte
    Interphase Components: Structure, Ion Transport, and Mechanical Properties.” <i>Chemistry
    of Materials</i>, vol. 30, no. 10, ACS, 2018, pp. 3338–45, doi:<a href="https://doi.org/10.1021/acs.chemmater.8b00750">10.1021/acs.chemmater.8b00750</a>.'
  short: L. Schafzahl, H. Ehmann, M. Kriechbaum, J. Sattelkow, T. Ganner, H. Plank,
    M. Wilkening, S.A. Freunberger, Chemistry of Materials 30 (2018) 3338–3345.
date_created: 2020-01-15T12:13:37Z
date_published: 2018-05-03T00:00:00Z
date_updated: 2021-01-12T08:12:46Z
day: '03'
doi: 10.1021/acs.chemmater.8b00750
extern: '1'
intvolume: '        30'
issue: '10'
language:
- iso: eng
month: '05'
oa_version: None
page: 3338-3345
publication: Chemistry of Materials
publication_identifier:
  eissn:
  - 1520-5002
  issn:
  - 0897-4756
publication_status: published
publisher: ACS
quality_controlled: '1'
status: public
title: 'Long-chain Li and Na alkyl carbonates as solid electrolyte interphase components:
  Structure, ion transport, and mechanical properties'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 30
year: '2018'
...
---
_id: '375'
abstract:
- lang: eng
  text: "Branched nanocrystals (NCs) enable high atomic surface exposure within a
    crystalline network that provides avenues for charge transport. This combination
    of properties makes branched NCs particularly suitable for a range of applications
    where both interaction with the media and charge transport are involved. Herein
    we report on the colloidal synthesis of branched ceria NCs by means of a ligand-mediated
    overgrowth mechanism. In particular, the differential coverage of oleic acid as
    an X-type ligand at ceria facets with different atomic density, atomic coordination
    deficiency, and oxygen vacancy density resulted in a preferential growth in the
    [111] direction and thus in the formation of ceria octapods. Alcohols, through
    an esterification alcoholysis reaction, promoted faster growth rates that translated
    into nanostructures with higher geometrical complexity, increasing the branch
    aspect ratio and triggering the formation of side branches. On the other hand,
    the presence of water resulted in a significant reduction of the growth rate,
    decreasing the reaction yield and eliminating side branching, which we associate
    to a blocking of the surface reaction sites or a displacement of the alcoholysis
    reaction. Overall, adjusting the amounts of each chemical, well-defined branched
    ceria NCs with tuned number, thickness, and length of branches and with overall
    size ranging from 5 to 45 nm could be produced. We further demonstrate that such
    branched ceria NCs are able to provide higher surface areas and related oxygen
    storage capacities (OSC) than quasi-spherical NCs.\r\n\r\n"
acknowledgement: This work was supported by the European Regional Development Funds
  and the Spanish MINECO project BOOSTER. T.B. is grateful for the FI-AGAUR Research
  Fellowship Program, Generalitat de Catalunya (2015 FI_B 00744). P.G. acknowledges
  the People Programme (Marie Curie Actions) of the FP7/2007-2013 European Union Program
  (TECNIOspring Grant Agreement No. 600388) and the Agency for Business Competitiveness
  of the Government of Catalonia, ACCIÓ. M.I. thanks AGAUR for Beatriu de Pinós postdoctoral
  grant (2013 BP-A00344). Z.L. thanks the China Scholarship Council for scholarship
  support.
article_processing_charge: No
article_type: original
author:
- first_name: Taisiia
  full_name: Berestok, Taisiia
  last_name: Berestok
- first_name: Pablo
  full_name: Guardia, Pablo
  last_name: Guardia
- first_name: Javier
  full_name: Blanco, Javier
  last_name: Blanco
- first_name: Raquel
  full_name: Nafria, Raquel
  last_name: Nafria
- first_name: Pau
  full_name: Torruella, Pau
  last_name: Torruella
- first_name: Luis
  full_name: López Conesa, Luis
  last_name: López Conesa
- first_name: Sònia
  full_name: Estradé, Sònia
  last_name: Estradé
- first_name: Maria
  full_name: Ibanez Sabate, Maria
  id: 43C61214-F248-11E8-B48F-1D18A9856A87
  last_name: Ibanez Sabate
  orcid: 0000-0001-5013-2843
- first_name: Jonathan
  full_name: De Roo, Jonathan
  last_name: De Roo
- first_name: Zhishan
  full_name: Luo, Zhishan
  last_name: Luo
- first_name: Doris
  full_name: Cadavid, Doris
  last_name: Cadavid
- first_name: José
  full_name: Martins, José
  last_name: Martins
- first_name: Maksym
  full_name: Kovalenko, Maksym
  last_name: Kovalenko
- first_name: Francesca
  full_name: Peiró, Francesca
  last_name: Peiró
- first_name: Andreu
  full_name: Cabot, Andreu
  last_name: Cabot
citation:
  ama: Berestok T, Guardia P, Blanco J, et al. Tuning branching in ceria nanocrystals.
    <i>Chemistry of Materials</i>. 2017;29(10):4418-4424. doi:<a href="https://doi.org/10.1021/acs.chemmater.7b00896">10.1021/acs.chemmater.7b00896</a>
  apa: Berestok, T., Guardia, P., Blanco, J., Nafria, R., Torruella, P., López Conesa,
    L., … Cabot, A. (2017). Tuning branching in ceria nanocrystals. <i>Chemistry of
    Materials</i>. American Chemical Society. <a href="https://doi.org/10.1021/acs.chemmater.7b00896">https://doi.org/10.1021/acs.chemmater.7b00896</a>
  chicago: Berestok, Taisiia, Pablo Guardia, Javier Blanco, Raquel Nafria, Pau Torruella,
    Luis López Conesa, Sònia Estradé, et al. “Tuning Branching in Ceria Nanocrystals.”
    <i>Chemistry of Materials</i>. American Chemical Society, 2017. <a href="https://doi.org/10.1021/acs.chemmater.7b00896">https://doi.org/10.1021/acs.chemmater.7b00896</a>.
  ieee: T. Berestok <i>et al.</i>, “Tuning branching in ceria nanocrystals,” <i>Chemistry
    of Materials</i>, vol. 29, no. 10. American Chemical Society, pp. 4418–4424, 2017.
  ista: Berestok T, Guardia P, Blanco J, Nafria R, Torruella P, López Conesa L, Estradé
    S, Ibáñez M, De Roo J, Luo Z, Cadavid D, Martins J, Kovalenko M, Peiró F, Cabot
    A. 2017. Tuning branching in ceria nanocrystals. Chemistry of Materials. 29(10),
    4418–4424.
  mla: Berestok, Taisiia, et al. “Tuning Branching in Ceria Nanocrystals.” <i>Chemistry
    of Materials</i>, vol. 29, no. 10, American Chemical Society, 2017, pp. 4418–24,
    doi:<a href="https://doi.org/10.1021/acs.chemmater.7b00896">10.1021/acs.chemmater.7b00896</a>.
  short: T. Berestok, P. Guardia, J. Blanco, R. Nafria, P. Torruella, L. López Conesa,
    S. Estradé, M. Ibáñez, J. De Roo, Z. Luo, D. Cadavid, J. Martins, M. Kovalenko,
    F. Peiró, A. Cabot, Chemistry of Materials 29 (2017) 4418–4424.
date_created: 2018-12-11T11:46:07Z
date_published: 2017-04-24T00:00:00Z
date_updated: 2024-03-05T12:19:17Z
day: '24'
doi: 10.1021/acs.chemmater.7b00896
extern: '1'
intvolume: '        29'
issue: '10'
language:
- iso: eng
month: '04'
oa_version: None
page: 4418 - 4424
publication: Chemistry of Materials
publication_identifier:
  eissn:
  - 1520-5002
  issn:
  - 0897-4756
publication_status: published
publisher: American Chemical Society
publist_id: '7455'
quality_controlled: '1'
status: public
title: Tuning branching in ceria nanocrystals
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 29
year: '2017'
...