化学
铟
电催化剂
二氧化碳
氧化物
异质结
无机化学
二氧化碳电化学还原
纳米技术
催化作用
电极
光电子学
一氧化碳
电化学
有机化学
物理化学
物理
材料科学
作者
Wanfeng Yang,Yong Zhao,Sheng Chen,Wenhao Ren,Xianjue Chen,Chen Jia,Zhen Su,Yuan Wang,Chuan Zhao
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2020-08-21
卷期号:59 (17): 12437-12444
被引量:67
标识
DOI:10.1021/acs.inorgchem.0c01544
摘要
Electrochemical CO2 reduction to fuels and chemicals is a promising approach for CO2 utilization. Developing highly active, selective, and cost-effective electrocatalysts is the key to the large-scale application of this technology. Here, we report that defective indium/indium oxide heterostructures selectively catalyze CO2 electroreduction into C1 products in a broad potential range from -0.7 to -1.2 V vs RHE in aqueous media with the faradaic efficiency approaching 100%. This electrocatalyst enables an efficient CO2-to-formate conversion with excellent selectivity (up to 93%), activity (up to 50.8 mA cm-2), and durability (>25 h). The collaboration between metallic In and In oxide of the heterostructures attributes to the boosted electrochemical CO2 reduction: Metallic In mainly facilitates formate production, while In oxide suppresses the competing hydrogen evolution reaction. This study highlights the integration of different functional components/defects into heterostructures as an effective strategy for enhancing CO2 electrocatalysis.
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