电催化剂
电解
氧化还原
催化作用
制氢
电化学
可逆氢电极
异质结
无机化学
氢
材料科学
化学工程
化学
电解水
电极
电解质
工作电极
有机化学
物理化学
工程类
光电子学
作者
Ruixing Du,Bing Wu,Weiling Tan,Yuchen Lei,Yunchuan Tu,Chalachew Mebrahtu,Zuohuan Chen,Shulong Li,Zuhui Zhou,Zhenchen Tang,Huanhao Chen,Shiming Chen,Long Chen,Jianjun Wang,Xiaofeng Shi,Yifan Ye,Dingsheng Wang,Regina Palkovits,Wei Zhao,Feng Zeng
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-08-04
卷期号:64 (38): e202510285-e202510285
被引量:14
标识
DOI:10.1002/anie.202510285
摘要
Abstract The coproduction of high‐value‐added acetate and hydrogen fuel by ethanol‐assisted water electrolysis is significant, but the efficiency of ethanol electrooxidation (EOR) is hindered both by sluggish kinetics, primarily dictated by the redox properties of the catalyst. Therefore, the development of efficient EOR electrocatalysts has to target optimized redox properties. Herein, a Ni 0 /Ni(OH) 2 heterostructure was synthesized by inducing a shift from hydrophilic to hydrophobic properties on the electrode surface during electrochemical deposition. The electrocatalyst enabled a current density of 573.7 mA cm −2 at 1.37 V versus RHE for EOR with a solar‐to‐hydrogen conversion efficiency of 14.4% when coupled to a commercial solar panel. Experimental and theoretical results disclosed that the incorporation of Ni 0 facilitates the ethanol to acetate kinetics through enhanced Ni 2+ to Ni 3+ conversion. The strategy, combining hydrogen production with the synthesis of value‐added products, enhances economic viability compared to conventional water electrolysis, underscoring its promise for practical implementation.
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