电催化剂
二氧化碳
催化作用
电化学
还原(数学)
乙醇
铜
晶界
二氧化碳电化学还原
材料科学
氧化物
电极
氧化铜
无机化学
冶金
化学工程
化学
一氧化碳
微观结构
数学
物理化学
有机化学
工程类
几何学
作者
Chao Yang,Hanchen Shen,Anxiang Guan,Junlang Liu,Tengfei Li,Yali Ji,Abdullah M. Al‐Enizi,Lijuan Zhang,Linping Qian,Gengfeng Zheng
标识
DOI:10.1016/j.jcis.2020.03.017
摘要
Electrochemical CO2 reduction with rationally designed copper-based electrocatalysts is a promising approach to reduce CO2 emission and produce value-added products. Grain boundaries and micron-strains inside catalysts have been proposed as active catalytic sites, while the controlled formation of these sites has remained highly challenging. In this work, we developed a strategy of creating high-density grain boundaries and micron-strains inside CuO electrocatalysts by fast cooling with liquid nitrogen. Compared to samples with slower cooling rates, the fast cooled CuO showed clear difference in their crystal domain sizes, micro-strain densities, and the chemisorption capacities of CO2 and CO. This micro-strain-rich CuO electrocatalyst exhibited a high total current density over 300 mA·cm-2, and an outstanding Faradaic efficiency for C2 products (with a majority to ethanol) at -1.0 V vs. reversible hydrogen electrode. Our work suggests a facile approach of tuning grain boundaries and micro-strains inside Cu-based electrocatalysts to scale up electrochemical CO2 reduction for high value-added products.
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