Recent Approaches for Cleaving the C─C Bond During Ethanol Electro‐Oxidation Reaction

Author:

Liang Chenjia1,Zhao Ruiyao1,Chen Teng12ORCID,Luo Yi2,Hu Jianqiang2,Qi Ping2,Ding Weiping1

Affiliation:

1. School of Chemistry and Chemical Engineering Nanjing University Nanjing Jiangsu 210023 China

2. Department of Aviation Oil and Material Air Force Logistics Academy Xuzhou Jiangsu 221000 China

Abstract

AbstractDirect ethanol fuel cells (DEFCs) play an indispensable role in the cyclic utilization of carbon resources due to its high volumetric energy density, high efficiency, and environmental benign character. However, owing to the chemically stable carbon‐carbon (C─C) bond of ethanol, its incomplete electrooxidation at the anode severely inhibits the energy and power density output of DEFCs. The efficiency of C─C bond cleaving on the state‐of‐the‐art Pt or Pd catalysts is reported as low as 7.5%. Recently, tremendous efforts are devoted to this field, and some effective strategies are put forward to facilitate the cleavage of the C─C bond. It is the right time to summarize the major breakthroughs in ethanol electrooxidation reaction. In this review, some optimization strategies including constructing core–shell nanostructure with alloying effect, doping other metal atoms in Pt and Pd catalysts, engineering composite catalyst with interface synergism, introducing cascade catalytic sites, and so on, are systematically summarized. In addition, the catalytic mechanism as well as the correlations between the catalyst structure and catalytic efficiency are further discussed. Finally, the prevailing limitations and feasible improvement directions for ethanol electrooxidation are proposed.

Funder

National Natural Science Foundation of China

China Postdoctoral Science Foundation

Publisher

Wiley

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