材料科学
法拉第效率
催化作用
电催化剂
电化学
可逆氢电极
硫系化合物
电解
电极
化学工程
金属
纳米技术
化学
光电子学
物理化学
冶金
工作电极
工程类
电解质
生物化学
作者
Fanrong Chen,Xiaoying Lü,Liang Ding,Zhen‐Hua Lyu,Jing Jing,Jiaju Fu,Jin‐Song Hu
标识
DOI:10.1002/smtd.202300957
摘要
Abstract Electrochemically converting CO 2 back into fuels and chemicals is promising in alleviating the greenhouse effect worldwide. Various high‐efficiency catalysts have been achieved, yet the unsatisfied structural stability under CO 2 electrolysis conditions restricts their practical application. Herein, a sub‐5 nm sized CuInS 2 quantum dots (CIS‐QDs) based electrocatalyst for converting CO 2 into CO are developed. Taking advantage of the stable M─Ch (metal‐chalcogenide) covalent bonds, and unique p‐block metal properties, the as‐prepared catalyst exhibits excellent structural stability under large overpotentials and can achieve a high CO Faradaic efficiency (FE) of 86% (total CO 2 reduction FE of 89%) at −0.65 V versus reversible hydrogen electrode with long‐term durability of 40 h and outstanding current densities of 10.6 mA cm −2 simultaneously. Furthermore, detailed electrochemical analyses revealed that the excellent performance of the as‐prepared catalysts shall be attributed to the high‐density active sites and fast charge transfer brought by the ultrasmall size of CIS‐QDs. This work provides insights into the design of high‐density and stable catalytic sites for developing high‐performance electrocatalysts.
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