Recent Approaches for Cleaving the C─C Bond During Ethanol Electro-Oxidation Reaction.
Chenjia LiangRuiyao ZhaoTeng ChenYi LuoJianqiang HuPing QiWeiping DingPublished in: Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2024)
Direct 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.
Keyphrases
- transition metal
- highly efficient
- high efficiency
- metal organic framework
- reduced graphene oxide
- electron transfer
- ionic liquid
- induced apoptosis
- room temperature
- gold nanoparticles
- quality improvement
- nitric oxide
- visible light
- risk assessment
- carbon dioxide
- human health
- cell cycle arrest
- signaling pathway
- cell proliferation