过电位
合理设计
电解质
催化作用
双金属片
选择性
电化学
碳氢化合物
化学
化学工程
无机化学
材料科学
纳米技术
电极
有机化学
工程类
物理化学
作者
Dunfeng Gao,Rosa M. Arán‐Ais,Hyo Sang Jeon,Beatriz Roldán Cuenya
出处
期刊:Nature Catalysis
[Springer Nature]
日期:2019-03-04
卷期号:2 (3): 198-210
被引量:1101
标识
DOI:10.1038/s41929-019-0235-5
摘要
The CO2 electroreduction reaction (CO2RR) to fuels and feedstocks is an attractive route to close the anthropogenic carbon cycle and store renewable energy. The generation of more reduced chemicals, especially multicarbon oxygenate and hydrocarbon products (C2+) with higher energy densities, is highly desirable for industrial applications. However, selective conversion of CO2 to C2+ suffers from a high overpotential, a low reaction rate and low selectivity, and the process is extremely sensitive to the catalyst structure and electrolyte. Here we discuss strategies to achieve high C2+ selectivity through rational design of the catalyst and electrolyte. Current state-of-the-art catalysts, including Cu and Cu–bimetallic catalysts, as well as some alternative materials, are considered. The importance of taking into consideration the dynamic evolution of the catalyst structure and composition are highlighted, focusing on findings extracted from in situ and operando characterizations. Additional theoretical insight into the reaction mechanisms underlying the improved C2+ selectivity of specific catalyst geometries and compositions in synergy with a well-chosen electrolyte are also provided. The electrochemical reduction of carbon dioxide to fuels and feedstocks has received increased attention over the past few years. In this Review, Roldan Cuenya and co-workers discuss strategies to achieve high selectivity towards multicarbon products via rational catalyst and electrolyte design.
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