Metallic Ni as Electron Acceptor Modulates the Redox of Catalytic Centers at Activated Ni <sup>0</sup> /Ni(OH) <sub>2</sub> Heterojunctions for Efficient Ethanol Electrooxidation

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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Publication Details

Journal
Angewandte Chemie
Published
2025-08-04
DOI
https://doi.org/10.1002/ange.202510285
Citations
1
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
0.36

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article

Metallic Ni as Electron Acceptor Modulates the Redox of Catalytic Centers at Activated Ni 0 /Ni(OH) 2 Heterojunctions for Efficient Ethanol Electrooxidation

Yunchuan Tu, Feng Zeng, Shulong Li, Ruixing Du et al.
1 citations
Angewandte Chemie
Electrocatalysts for Energy Conversion
0.36
article

Metallic Ni as Electron Acceptor Modulates the Redox of Catalytic Centers at Activated Ni 0 /Ni(OH) 2 Heterojunctions for Efficient Ethanol Electrooxidation

Yunchuan Tu, Feng Zeng, Shulong Li, Ruixing Du, Huanhao Chen, Dingsheng S. Wang, Yuchen Lei, Bing Wu, Zhenchen Tang, Wei Zhao, Regina Palkovits, Chalachew Mebrahtu, Weiling Tan, Long Chen, Yifan Ye, Shiming Chen, Zuohuan Chen, Xiaofeng Shi, Zuhui Zhou, Jianjun Wang
article en
1 citations

Abstract

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.

Angewandte ChemieVol. 137(38)
University of Science and Technology of China (CN), Nanjing Tech University (CN), North University of China (CN), Shandong University (CN), Chongqing University (CN), Forschungszentrum Jülich (DE), Nanyang Technological University (SG), Shenzhen University (CN), Chengdu University (CN), National Synchrotron Radiation Laboratory (CN), State Key Laboratory of Crystal Materials, RWTH Aachen University (DE), China Medical University (CN), Tsinghua University (CN)
National Research Foundation, China Postdoctoral Science Foundation, Basic and Applied Basic Research Foundation of Guangdong Province
Openalex Percentile: Top 41%
Electrocatalysts for Energy Conversion
0.36
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