---
_id: '14828'
abstract:
- lang: eng
text: Production of hydrogen at large scale requires development of non-noble, inexpensive,
and high-performing catalysts for constructing water-splitting devices. Herein,
we report the synthesis of Zn-doped NiO heterostructure (ZnNiO) catalysts at room
temperature via a coprecipitation method followed by drying (at 80 °C, 6 h) and
calcination at an elevated temperature of 400 °C for 5 h under three distinct
conditions, namely, air, N2, and vacuum. The vacuum-synthesized catalyst demonstrates
a low overpotential of 88 mV at −10 mA cm–2 and a small Tafel slope of 73 mV dec–1
suggesting relatively higher charge transfer kinetics for hydrogen evolution reactions
(HER) compared with the specimens synthesized under N2 or O2 atmosphere. It also
demonstrates an oxygen evolution (OER) overpotential of 260 mV at 10 mA cm–2 with
a low Tafel slope of 63 mV dec–1. In a full-cell water-splitting device, the vacuum-synthesized
ZnNiO heterostructure demonstrates a cell voltage of 1.94 V at 50 mA cm–2 and
shows remarkable stability over 24 h at a high current density of 100 mA cm–2.
It is also demonstrated in this study that Zn-doping, surface, and interface engineering
in transition-metal oxides play a crucial role in efficient electrocatalytic water
splitting. Also, the results obtained from density functional theory (DFT + U
= 0–8 eV), where U is the on-site Coulomb repulsion parameter also known as Hubbard
U, based electronic structure calculations confirm that Zn doping constructively
modifies the electronic structure, in both the valence band and the conduction
band, and found to be suitable in tailoring the carrier’s effective masses of
electrons and holes. The decrease in electron’s effective masses together with
large differences between the effective masses of electrons and holes is noticed,
which is found to be mainly responsible for achieving the best water-splitting
performance from a 9% Zn-doped NiO sample prepared under vacuum.
acknowledgement: This work was supported by the Technology Innovation Program (20011622,
Development of Battery System Applied High-Efficiency Heat Control Polymer and Part
Component) funded by the Ministry of Trade, Industry & Energy (MOTIE, Korea). Author
acknowledge to Prof. Tsunehiro Takeuchi from Toyota Technological Institute, Nagoya,
Japan for the support of computational resources.
article_processing_charge: No
article_type: original
author:
- first_name: Gundegowda Kalligowdanadoddi
full_name: Kiran, Gundegowda Kalligowdanadoddi
last_name: Kiran
- first_name: Saurabh
full_name: Singh, Saurabh
id: 12d625da-9cb3-11ed-9667-af09d37d3f0a
last_name: Singh
orcid: 0000-0003-2209-5269
- first_name: Neelima
full_name: Mahato, Neelima
last_name: Mahato
- first_name: Thupakula Venkata Madhukar
full_name: Sreekanth, Thupakula Venkata Madhukar
last_name: Sreekanth
- first_name: Gowra Raghupathy
full_name: Dillip, Gowra Raghupathy
last_name: Dillip
- first_name: Kisoo
full_name: Yoo, Kisoo
last_name: Yoo
- first_name: Jonghoon
full_name: Kim, Jonghoon
last_name: Kim
citation:
ama: Kiran GK, Singh S, Mahato N, et al. Interface engineering modulation combined
with electronic structure modification of Zn-doped NiO heterostructure for efficient
water-splitting activity. ACS Applied Energy Materials. 2024;7(1):214-229.
doi:10.1021/acsaem.3c02519
apa: Kiran, G. K., Singh, S., Mahato, N., Sreekanth, T. V. M., Dillip, G. R., Yoo,
K., & Kim, J. (2024). Interface engineering modulation combined with electronic
structure modification of Zn-doped NiO heterostructure for efficient water-splitting
activity. ACS Applied Energy Materials. American Chemical Society. https://doi.org/10.1021/acsaem.3c02519
chicago: Kiran, Gundegowda Kalligowdanadoddi, Saurabh Singh, Neelima Mahato, Thupakula
Venkata Madhukar Sreekanth, Gowra Raghupathy Dillip, Kisoo Yoo, and Jonghoon Kim.
“Interface Engineering Modulation Combined with Electronic Structure Modification
of Zn-Doped NiO Heterostructure for Efficient Water-Splitting Activity.” ACS
Applied Energy Materials. American Chemical Society, 2024. https://doi.org/10.1021/acsaem.3c02519.
ieee: G. K. Kiran et al., “Interface engineering modulation combined with
electronic structure modification of Zn-doped NiO heterostructure for efficient
water-splitting activity,” ACS Applied Energy Materials, vol. 7, no. 1.
American Chemical Society, pp. 214–229, 2024.
ista: Kiran GK, Singh S, Mahato N, Sreekanth TVM, Dillip GR, Yoo K, Kim J. 2024.
Interface engineering modulation combined with electronic structure modification
of Zn-doped NiO heterostructure for efficient water-splitting activity. ACS Applied
Energy Materials. 7(1), 214–229.
mla: Kiran, Gundegowda Kalligowdanadoddi, et al. “Interface Engineering Modulation
Combined with Electronic Structure Modification of Zn-Doped NiO Heterostructure
for Efficient Water-Splitting Activity.” ACS Applied Energy Materials,
vol. 7, no. 1, American Chemical Society, 2024, pp. 214–29, doi:10.1021/acsaem.3c02519.
short: G.K. Kiran, S. Singh, N. Mahato, T.V.M. Sreekanth, G.R. Dillip, K. Yoo, J.
Kim, ACS Applied Energy Materials 7 (2024) 214–229.
date_created: 2024-01-17T12:48:35Z
date_published: 2024-01-08T00:00:00Z
date_updated: 2024-01-22T13:47:39Z
day: '08'
department:
- _id: MaIb
doi: 10.1021/acsaem.3c02519
external_id:
isi:
- '001138342900001'
intvolume: ' 7'
isi: 1
issue: '1'
keyword:
- Electrical and Electronic Engineering
- Materials Chemistry
- Electrochemistry
- Energy Engineering and Power Technology
- Chemical Engineering (miscellaneous)
language:
- iso: eng
month: '01'
oa_version: None
page: 214-229
publication: ACS Applied Energy Materials
publication_identifier:
issn:
- 2574-0962
publication_status: published
publisher: American Chemical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: Interface engineering modulation combined with electronic structure modification
of Zn-doped NiO heterostructure for efficient water-splitting activity
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 7
year: '2024'
...
---
_id: '15114'
abstract:
- lang: eng
text: As a key liquid organic hydrogen carrier, investigating the decomposition
of formic acid (HCOOH) on the Pd (1 1 1) transition metal surface is imperative
for harnessing hydrogen energy. Despite a multitude of studies, the major mechanisms
and key intermediates involved in the dehydrogenation process of formic acid remain
a great topic of debate due to ambiguous adsorbate interactions. In this research,
we develop an advanced microkinetic model based on first-principles calculations,
accounting for adsorbate–adsorbate interactions. Our study unveils a comprehensive
mechanism for the Pd (1 1 1) surface, highlighting the significance of coverage
effects in formic acid dehydrogenation. Our findings unequivocally demonstrate
that H coverage on the Pd (1 1 1) surface renders formic acid more susceptible
to decompose into H2 and CO2 through COOH intermediates. Consistent with experimental
results, the selectivity of H2 in the decomposition of formic acid on the Pd (1
1 1) surface approaches 100 %. Considering the influence of H coverage, our kinetic
analysis aligns perfectly with experimental values at a temperature of 373 K.
acknowledgement: The authors acknowledge the financial support from the National Key
Research and Development Project of China (2021YFA1500900, 2022YFE0113800), the
National Natural Science Foundation of China (22141001, U21A20298), Zhejiang Innovation
Team (2017R5203).
article_number: '119959'
article_processing_charge: No
article_type: original
author:
- first_name: Zihao
full_name: Yao, Zihao
last_name: Yao
- first_name: Xu
full_name: Liu, Xu
last_name: Liu
- first_name: Rhys
full_name: Bunting, Rhys
id: 91deeae8-1207-11ec-b130-c194ad5b50c6
last_name: Bunting
orcid: 0000-0001-6928-074X
- first_name: Jianguo
full_name: Wang, Jianguo
last_name: Wang
citation:
ama: 'Yao Z, Liu X, Bunting R, Wang J. Unravelling the reaction mechanism for H2
production via formic acid decomposition over Pd: Coverage-dependent microkinetic
modeling. Chemical Engineering Science. 2024;291. doi:10.1016/j.ces.2024.119959'
apa: 'Yao, Z., Liu, X., Bunting, R., & Wang, J. (2024). Unravelling the reaction
mechanism for H2 production via formic acid decomposition over Pd: Coverage-dependent
microkinetic modeling. Chemical Engineering Science. Elsevier. https://doi.org/10.1016/j.ces.2024.119959'
chicago: 'Yao, Zihao, Xu Liu, Rhys Bunting, and Jianguo Wang. “Unravelling the Reaction
Mechanism for H2 Production via Formic Acid Decomposition over Pd: Coverage-Dependent
Microkinetic Modeling.” Chemical Engineering Science. Elsevier, 2024. https://doi.org/10.1016/j.ces.2024.119959.'
ieee: 'Z. Yao, X. Liu, R. Bunting, and J. Wang, “Unravelling the reaction mechanism
for H2 production via formic acid decomposition over Pd: Coverage-dependent microkinetic
modeling,” Chemical Engineering Science, vol. 291. Elsevier, 2024.'
ista: 'Yao Z, Liu X, Bunting R, Wang J. 2024. Unravelling the reaction mechanism
for H2 production via formic acid decomposition over Pd: Coverage-dependent microkinetic
modeling. Chemical Engineering Science. 291, 119959.'
mla: 'Yao, Zihao, et al. “Unravelling the Reaction Mechanism for H2 Production via
Formic Acid Decomposition over Pd: Coverage-Dependent Microkinetic Modeling.”
Chemical Engineering Science, vol. 291, 119959, Elsevier, 2024, doi:10.1016/j.ces.2024.119959.'
short: Z. Yao, X. Liu, R. Bunting, J. Wang, Chemical Engineering Science 291 (2024).
date_created: 2024-03-17T23:00:57Z
date_published: 2024-03-04T00:00:00Z
date_updated: 2024-03-19T08:47:42Z
day: '04'
department:
- _id: MaIb
doi: 10.1016/j.ces.2024.119959
intvolume: ' 291'
language:
- iso: eng
month: '03'
oa_version: None
publication: Chemical Engineering Science
publication_identifier:
issn:
- 0009-2509
publication_status: epub_ahead
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Unravelling the reaction mechanism for H2 production via formic acid decomposition
over Pd: Coverage-dependent microkinetic modeling'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 291
year: '2024'
...
---
_id: '15182'
abstract:
- lang: eng
text: Thermoelectric materials convert heat into electricity, with a broad range
of applications near room temperature (RT). However, the library of RT high-performance
materials is limited. Traditional high-temperature synthetic methods constrain
the range of materials achievable, hindering the ability to surpass crystal structure
limitations and engineer defects. Here, a solution-based synthetic approach is
introduced, enabling RT synthesis of powders and exploration of densification
at lower temperatures to influence the material's microstructure. The approach
is exemplified by Ag2Se, an n-type alternative to bismuth telluride. It is demonstrated
that the concentration of Ag interstitials, grain boundaries, and dislocations
are directly correlated to the sintering temperature, and achieve a figure of
merit of 1.1 from RT to 100 °C after optimization. Moreover, insights into and
resolve Ag2Se's challenges are provided, including stoichiometry issues leading
to irreproducible performances. This work highlights the potential of RT solution
synthesis in expanding the repertoire of high-performance thermoelectric materials
for practical applications.
acknowledged_ssus:
- _id: EM-Fac
- _id: LifeSc
- _id: NanoFab
acknowledgement: This work was supported by the Scientific Service Units (SSU) of
ISTA through resources provided by the Electron Microscopy Facility (EMF), the Lab
Support Facility (LSF), and the Nanofabrication Facility (NNF). This work was financially
supported by ISTA and the Werner Siemens Foundation. The USTEM Service Unit of the
Technical University of Vienna is acknowledged for EBSD sample preparation and analysis.
R.L.B. acknowledges the National Science Foundation for funding the mass spectrometry
analysis under award DMR 1904719. J.L. is a Serra Húnter Fellow and is grateful
to the ICREA Academia program and projects MICINN/FEDER PID2021-124572OB-C31 and
GC 2021 SGR 01061.
article_number: '2400408'
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Tobias
full_name: Kleinhanns, Tobias
id: 8BD9DE16-AB3C-11E9-9C8C-2A03E6697425
last_name: Kleinhanns
- first_name: Francesco
full_name: Milillo, Francesco
id: 38b830db-ea88-11ee-bf9b-929beaf79054
last_name: Milillo
- first_name: Mariano
full_name: Calcabrini, Mariano
id: 45D7531A-F248-11E8-B48F-1D18A9856A87
last_name: Calcabrini
orcid: 0000-0003-4566-5877
- first_name: Christine
full_name: Fiedler, Christine
id: bd3fceba-dc74-11ea-a0a7-c17f71817366
last_name: Fiedler
- first_name: Sharona
full_name: Horta, Sharona
id: 03a7e858-01b1-11ec-8b71-99ae6c4a05bc
last_name: Horta
- first_name: Daniel
full_name: Balazs, Daniel
id: 302BADF6-85FC-11EA-9E3B-B9493DDC885E
last_name: Balazs
orcid: 0000-0001-7597-043X
- first_name: Marissa J.
full_name: Strumolo, Marissa J.
last_name: Strumolo
- first_name: Roger
full_name: Hasler, Roger
last_name: Hasler
- first_name: Jordi
full_name: Llorca, Jordi
last_name: Llorca
- first_name: Michael
full_name: Tkadletz, Michael
last_name: Tkadletz
- first_name: Richard L.
full_name: Brutchey, Richard L.
last_name: Brutchey
- first_name: Maria
full_name: Ibáñez, Maria
id: 43C61214-F248-11E8-B48F-1D18A9856A87
last_name: Ibáñez
orcid: 0000-0001-5013-2843
citation:
ama: 'Kleinhanns T, Milillo F, Calcabrini M, et al. A route to high thermoelectric
performance: Solution‐based control of microstructure and composition in Ag2Se.
Advanced Energy Materials. 2024. doi:10.1002/aenm.202400408'
apa: 'Kleinhanns, T., Milillo, F., Calcabrini, M., Fiedler, C., Horta, S., Balazs,
D., … Ibáñez, M. (2024). A route to high thermoelectric performance: Solution‐based
control of microstructure and composition in Ag2Se. Advanced Energy Materials.
Wiley. https://doi.org/10.1002/aenm.202400408'
chicago: 'Kleinhanns, Tobias, Francesco Milillo, Mariano Calcabrini, Christine Fiedler,
Sharona Horta, Daniel Balazs, Marissa J. Strumolo, et al. “A Route to High Thermoelectric
Performance: Solution‐based Control of Microstructure and Composition in Ag2Se.”
Advanced Energy Materials. Wiley, 2024. https://doi.org/10.1002/aenm.202400408.'
ieee: 'T. Kleinhanns et al., “A route to high thermoelectric performance:
Solution‐based control of microstructure and composition in Ag2Se,” Advanced
Energy Materials. Wiley, 2024.'
ista: 'Kleinhanns T, Milillo F, Calcabrini M, Fiedler C, Horta S, Balazs D, Strumolo
MJ, Hasler R, Llorca J, Tkadletz M, Brutchey RL, Ibáñez M. 2024. A route to high
thermoelectric performance: Solution‐based control of microstructure and composition
in Ag2Se. Advanced Energy Materials., 2400408.'
mla: 'Kleinhanns, Tobias, et al. “A Route to High Thermoelectric Performance: Solution‐based
Control of Microstructure and Composition in Ag2Se.” Advanced Energy Materials,
2400408, Wiley, 2024, doi:10.1002/aenm.202400408.'
short: T. Kleinhanns, F. Milillo, M. Calcabrini, C. Fiedler, S. Horta, D. Balazs,
M.J. Strumolo, R. Hasler, J. Llorca, M. Tkadletz, R.L. Brutchey, M. Ibáñez, Advanced
Energy Materials (2024).
date_created: 2024-03-25T08:57:40Z
date_published: 2024-03-13T00:00:00Z
date_updated: 2024-03-25T09:21:05Z
day: '13'
department:
- _id: MaIb
- _id: LifeSc
doi: 10.1002/aenm.202400408
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1002/aenm.202400408
month: '03'
oa: 1
oa_version: Published Version
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 Energy Materials
publication_identifier:
eissn:
- 1614-6840
issn:
- 1614-6832
publication_status: epub_ahead
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'A route to high thermoelectric performance: Solution‐based control of microstructure
and composition in Ag2Se'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2024'
...
---
_id: '15166'
abstract:
- lang: eng
text: Reducing defects boosts room-temperature performance of a thermoelectric device
acknowledgement: The authors thank the Werner-Siemens-Stiftung and the Institute of
Science and Technology Austria for financial support.
article_processing_charge: No
article_type: letter_note
author:
- first_name: Navita
full_name: Navita, Navita
id: 6ebe278d-ba0b-11ee-8184-f34cdc671de4
last_name: Navita
- first_name: Maria
full_name: Ibáñez, Maria
id: 43C61214-F248-11E8-B48F-1D18A9856A87
last_name: Ibáñez
orcid: 0000-0001-5013-2843
citation:
ama: Jakhar N, Ibáñez M. Electron highways are cooler. Science. 2024;383(6688):1184.
doi:10.1126/science.ado4077
apa: Jakhar, N., & Ibáñez, M. (2024). Electron highways are cooler. Science.
American Association for the Advancement of Science. https://doi.org/10.1126/science.ado4077
chicago: Jakhar, Navita, and Maria Ibáñez. “Electron Highways Are Cooler.” Science.
American Association for the Advancement of Science, 2024. https://doi.org/10.1126/science.ado4077.
ieee: N. Jakhar and M. Ibáñez, “Electron highways are cooler,” Science, vol.
383, no. 6688. American Association for the Advancement of Science, p. 1184, 2024.
ista: Jakhar N, Ibáñez M. 2024. Electron highways are cooler. Science. 383(6688),
1184.
mla: Jakhar, Navita, and Maria Ibáñez. “Electron Highways Are Cooler.” Science,
vol. 383, no. 6688, American Association for the Advancement of Science, 2024,
p. 1184, doi:10.1126/science.ado4077.
short: N. Jakhar, M. Ibáñez, Science 383 (2024) 1184.
date_created: 2024-03-24T23:00:58Z
date_published: 2024-03-14T00:00:00Z
date_updated: 2024-03-25T10:31:20Z
day: '14'
department:
- _id: MaIb
doi: 10.1126/science.ado4077
intvolume: ' 383'
issue: '6688'
language:
- iso: eng
month: '03'
oa_version: None
page: '1184'
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: Science
publication_identifier:
eissn:
- 1095-9203
issn:
- 0036-8075
publication_status: published
publisher: American Association for the Advancement of Science
quality_controlled: '1'
scopus_import: '1'
status: public
title: Electron highways are cooler
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 383
year: '2024'
...
---
_id: '12832'
abstract:
- lang: eng
text: The development of cost-effective, high-activity and stable bifunctional catalysts
for the oxygen reduction and evolution reactions (ORR/OER) is essential for zinc–air
batteries (ZABs) to reach the market. Such catalysts must contain multiple adsorption/reaction
sites to cope with the high demands of reversible oxygen electrodes. Herein, we
propose a high entropy alloy (HEA) based on relatively abundant elements as a
bifunctional ORR/OER catalyst. More specifically, we detail the synthesis of a
CrMnFeCoNi HEA through a low-temperature solution-based approach. Such HEA displays
superior OER performance with an overpotential of 265 mV at a current density
of 10 mA/cm2, and a 37.9 mV/dec Tafel slope, well above the properties of a standard
commercial catalyst based on RuO2. This high performance is partially explained
by the presence of twinned defects, the incidence of large lattice distortions,
and the electronic synergy between the different components, being Cr key to decreasing
the energy barrier of the OER rate-determining step. CrMnFeCoNi also displays
superior ORR performance with a half-potential of 0.78 V and an onset potential
of 0.88 V, comparable with commercial Pt/C. The potential gap (Egap) between the
OER overpotential and the ORR half-potential of CrMnFeCoNi is just 0.734 V. Taking
advantage of these outstanding properties, ZABs are assembled using the CrMnFeCoNi
HEA as air cathode and a zinc foil as the anode. The assembled cells provide an
open-circuit voltage of 1.489 V, i.e. 90% of its theoretical limit (1.66 V), a
peak power density of 116.5 mW/cm2, and a specific capacity of 836 mAh/g that
stays stable for more than 10 days of continuous cycling, i.e. 720 cycles @ 8
mA/cm2 and 16.6 days of continuous cycling, i.e. 1200 cycles @ 5 mA/cm2.
acknowledged_ssus:
- _id: EM-Fac
acknowledgement: 'The authors thank the support from the project COMBENERGY, PID2019-105490RB-C32,
from the Spanish Ministerio de Ciencia e Innovación. The authors acknowledge funding
from Generalitat de Catalunya 2021 SGR 01581 and 2021 SGR 00457. ICN2 acknowledges
the Severo Ochoa program from Spanish MINECO (Grant No. SEV-2017-0706). IREC and
ICN2 are funded by the CERCA Programme from the Generalitat de Catalunya. ICN2 is
supported by the Severo Ochoa program from Spanish MCIN / AEI (Grant No.: CEX2021-001214-S).
ICN2 acknowledges funding from Generalitat de Catalunya 2017 SGR 327. This study
was supported by MCIN with funding from European Union NextGenerationEU (PRTR-C17.I1)
and Generalitat de Catalunya. The authors thank the support from the project NANOGEN
(PID2020-116093RB-C43), funded by MCIN/ AEI/10.13039/501100011033/ and by “ERDF
A way of making Europe”, by the “European Union”. Part of the present work has been
performed in the frameworks of Universitat de Barcelona Nanoscience PhD program.
This research was supported by the Scientific Service Units (SSU) of IST Austria
through resources provided by Electron Microscopy Facility (EMF). S. Lee. and M.
Ibáñez acknowledge funding by IST Austria and the Werner Siemens Foundation. J.
Llorca is a Serra Húnter Fellow and is grateful to ICREA Academia program and projects
MICINN/FEDER PID2021-124572OB-C31 and GC 2017 SGR 128. L. L.Yang thanks the China
Scholarship Council (CSC) for the scholarship support (202008130132). Z. F. Liang
acknowledges funding from MINECO SO-FPT PhD grant (SEV-2013-0295-17-1). J. W. Chen
and Y. Xu thank the support from The Key Research and Development Program of Hebei
Province (No. 20314305D) and the cooperative scientific research project of the
“Chunhui Program” of the Ministry of Education (2018-7). This work was supported
by the Natural Science Foundation of Sichuan province (NSFSC) and funded by the
Science and Technology Department of Sichuan Province (2022NSFSC1229).'
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: Xiang
full_name: Wang, Xiang
last_name: Wang
- first_name: Seungho
full_name: Lee, Seungho
id: BB243B88-D767-11E9-B658-BC13E6697425
last_name: Lee
orcid: 0000-0002-6962-8598
- first_name: Ting
full_name: Zhang, Ting
last_name: Zhang
- first_name: Lingxiao
full_name: Li, Lingxiao
last_name: Li
- first_name: Zhifu
full_name: Liang, Zhifu
last_name: Liang
- first_name: Jingwei
full_name: Chen, Jingwei
last_name: Chen
- first_name: Junshan
full_name: Li, Junshan
last_name: Li
- first_name: Ahmad
full_name: Ostovari Moghaddam, Ahmad
last_name: Ostovari Moghaddam
- 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: Jordi
full_name: Arbiol, Jordi
last_name: Arbiol
- first_name: Ying
full_name: Xu, Ying
last_name: Xu
- first_name: Andreu
full_name: Cabot, Andreu
last_name: Cabot
citation:
ama: He R, Yang L, Zhang Y, et al. A CrMnFeCoNi high entropy alloy boosting oxygen
evolution/reduction reactions and zinc-air battery performance. Energy Storage
Materials. 2023;58(4):287-298. doi:10.1016/j.ensm.2023.03.022
apa: He, R., Yang, L., Zhang, Y., Wang, X., Lee, S., Zhang, T., … Cabot, A. (2023).
A CrMnFeCoNi high entropy alloy boosting oxygen evolution/reduction reactions
and zinc-air battery performance. Energy Storage Materials. Elsevier. https://doi.org/10.1016/j.ensm.2023.03.022
chicago: He, Ren, Linlin Yang, Yu Zhang, Xiang Wang, Seungho Lee, Ting Zhang, Lingxiao
Li, et al. “A CrMnFeCoNi High Entropy Alloy Boosting Oxygen Evolution/Reduction
Reactions and Zinc-Air Battery Performance.” Energy Storage Materials.
Elsevier, 2023. https://doi.org/10.1016/j.ensm.2023.03.022.
ieee: R. He et al., “A CrMnFeCoNi high entropy alloy boosting oxygen evolution/reduction
reactions and zinc-air battery performance,” Energy Storage Materials,
vol. 58, no. 4. Elsevier, pp. 287–298, 2023.
ista: He R, Yang L, Zhang Y, Wang X, Lee S, Zhang T, Li L, Liang Z, Chen J, Li J,
Ostovari Moghaddam A, Llorca J, Ibáñez M, Arbiol J, Xu Y, Cabot A. 2023. A CrMnFeCoNi
high entropy alloy boosting oxygen evolution/reduction reactions and zinc-air
battery performance. Energy Storage Materials. 58(4), 287–298.
mla: He, Ren, et al. “A CrMnFeCoNi High Entropy Alloy Boosting Oxygen Evolution/Reduction
Reactions and Zinc-Air Battery Performance.” Energy Storage Materials,
vol. 58, no. 4, Elsevier, 2023, pp. 287–98, doi:10.1016/j.ensm.2023.03.022.
short: R. He, L. Yang, Y. Zhang, X. Wang, S. Lee, T. Zhang, L. Li, Z. Liang, J.
Chen, J. Li, A. Ostovari Moghaddam, J. Llorca, M. Ibáñez, J. Arbiol, Y. Xu, A.
Cabot, Energy Storage Materials 58 (2023) 287–298.
date_created: 2023-04-16T22:01:07Z
date_published: 2023-04-01T00:00:00Z
date_updated: 2023-08-01T14:08:02Z
day: '01'
department:
- _id: MaIb
doi: 10.1016/j.ensm.2023.03.022
external_id:
isi:
- '000967601700001'
intvolume: ' 58'
isi: 1
issue: '4'
language:
- iso: eng
month: '04'
oa_version: None
page: 287-298
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: Energy Storage Materials
publication_identifier:
eissn:
- 2405-8297
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: A CrMnFeCoNi high entropy alloy boosting oxygen evolution/reduction reactions
and zinc-air battery performance
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 58
year: '2023'
...