金属与支撑物的相互作用促进了金催化剂在氢气进化耦合乙醇电氧化反应中的应用

IF 2.6 4区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY ChemNanoMat Pub Date : 2024-07-12 DOI:10.1002/cnma.202400267
Yiquan Yin, Dr. Fangwei Gu, Yuxin Wang, Chengjin Chen, Yongsheng Wang, Prof. Wei Zhu, Prof. Zhongbin Zhuang
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引用次数: 0

摘要

利用乙醇进行电化学制氢和醋酸联产是一种前景广阔的绿色制氢技术,具有制氢能耗低、收益高的特点。然而,阳极乙醇电氧化反应(EOR)的催化稳定性较差,阻碍了该装置的应用。我们采用金属支撑相互作用策略,利用硫化亚铜支撑强化小尺寸金活性位点。Au-Cu2-xS/C 在 1.1 V 对 RHE 时显示出 1055 mA mgAu-1 的卓越活性,并在计时电位测试中保持了高活性,超过了 Au/C 催化剂。研究表明,Cu2-xS 支持物促进了 Au-OH 的形成,并阻止了金位点的聚集,从而提高了 EOR 的活性和稳定性。最后,使用 Au-Cu2-xS/C 阳极催化剂组装的电化学热电联产电解槽连续运行了 100 多个小时,表明了该装置的适用性。
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Metal-Support Interaction Boosts Au Catalysts for Hydrogen Evolution-Coupled Ethanol Electro-Oxidation Reaction

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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来源期刊
ChemNanoMat
ChemNanoMat Energy-Energy Engineering and Power Technology
CiteScore
6.10
自引率
2.60%
发文量
236
期刊介绍: ChemNanoMat is a new journal published in close cooperation with the teams of Angewandte Chemie and Advanced Materials, and is the new sister journal to Chemistry—An Asian Journal.
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