journal article·2024-10

Metal‐Support Interaction Boosts Au Catalysts for Hydrogen Evolution‐Coupled Ethanol Electro‐Oxidation Reaction

Yiquan Yin, Fangwei Gu, Yuxin Wang, Chengjin Chen, Yongsheng Wang, Wei Zhu, Zhongbin Zhuang

ChemNanoMat· Volume 10· Issue 10
Publisher page

Abstract

Abstract Electrochemical hydrogen and acetate cogeneration from ethanol is a promising green hydrogen production technique with low hydrogen production energy consumption and high profitability. However, the poor catalytic stability of the anodic ethanol electro‐oxidation reaction (EOR) retards the device application. We adopted a metal support interaction strategy to reinforce small‐sized Au active sites using cuprous sulfide supports. The Au−Cu2–xS/C showed a superior activity of 1055 mA mgAu−1 at 1.1 V vs. RHE and retained the high activity in the chronopotentiometric test, surpassing the Au/C catalyst. It was demonstrated that the Cu2–xS support facilitated the formation of Au−OH and prevented the gold sites from aggregation, leading to high activity and stability for EOR. Finally, an electrochemical cogeneration electrolyzer assembled with the Au−Cu2–xS/C anodic catalyst continuously ran for over 100 hours, suggesting the device‘s applicability.
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Research context

OpenAlex topics: Electrocatalysts for Energy Conversion · Catalytic Processes in Materials Science · CO2 Reduction Techniques and Catalysts

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

State Key Lab of Organic-Inorganic Composites and Beijing Advanced Innovation Center for Soft Matter Science and Engineering Beijing University of Chemical Technology Beijing 100029 China

State Key Laboratory of Catalytic Materials and Reaction Engineering Research Institute of Petroleum Processing Beijing 100083 China

Beijing Key Laboratory of Energy Environmental Catalysis Beijing University of Chemical Technology Beijing 100029 China

Funding

National Natural Science Foundation of China

References (34)

Show source-provided references
1. 10.1016/j.ijhydene.2022.02.11210.1016/j.ijhydene.2022.02.112 ↗
2.
3. 10.1016/j.cjche.2022.02.01010.1016/j.cjche.2022.02.010 ↗
4. 10.1007/s12274-023-5502-810.1007/s12274-023-5502-8 ↗
5.
6. 10.1039/C8TA03741H10.1039/C8TA03741H ↗
7. Chen W. S. · Chem. J. Chinese U. · 2022 · 43
8. 10.1007/s12274-021-3930-x10.1007/s12274-021-3930-x ↗
9. 10.1007/s12274-023-6023-110.1007/s12274-023-6023-1 ↗
10.
11. Rao L. · Prog. Chem. · 2014 · 26 · 727
12. 10.3390/catal503150710.3390/catal5031507 ↗
13. 10.1016/j.jpowsour.2007.04.00910.1016/j.jpowsour.2007.04.009 ↗
14. 10.1002/cssc.20180306310.1002/cssc.201803063 ↗
15. 10.1039/C4CP00394B10.1039/C4CP00394B ↗
16. 10.1021/ja200976j10.1021/ja200976j ↗
17.
18. 10.1002/adma.20200330010.1002/adma.202003300 ↗
19. 10.1007/s12274-021-3363-610.1007/s12274-021-3363-6 ↗
20. 10.1021/jacs.2c1186110.1021/jacs.2c11861 ↗
21. 10.1002/cnma.20200066510.1002/cnma.202000665 ↗
22. 10.1039/D0NJ03219K10.1039/D0NJ03219K ↗
23.
24. 10.1016/j.chempr.2019.04.02410.1016/j.chempr.2019.04.024 ↗
25. 10.1016/j.cej.2019.12261310.1016/j.cej.2019.122613 ↗
26. 10.1021/acsami.0c1342010.1021/acsami.0c13420 ↗
27. 10.1002/chem.20210139210.1002/chem.202101392 ↗
28. 10.1038/s41467-023-44664-310.1038/s41467-023-44664-3 ↗
29. 10.1351/pac19916305071110.1351/pac199163050711 ↗
30. 10.1039/dt991000312110.1039/dt9910003121 ↗
31. 10.1016/j.jcat.2013.11.02010.1016/j.jcat.2013.11.020 ↗
32.
33. 10.1021/acscatal.9b0013810.1021/acscatal.9b00138 ↗
34. 10.1016/j.apcatb.2016.08.06310.1016/j.apcatb.2016.08.063 ↗