格式化
铋
密度泛函理论
材料科学
原位
法拉第效率
催化作用
纳米技术
还原(数学)
可逆氢电极
选择性
化学
化学工程
无机化学
计算化学
电极
物理化学
电化学
有机化学
冶金
生物化学
几何学
数学
参比电极
工程类
作者
Youzeng Li,Jialei Chen,Shan Chen,Xuelong Liao,Tete Zhao,Fangyi Cheng,Huan Wang
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2022-03-23
卷期号:7 (4): 1454-1461
被引量:122
标识
DOI:10.1021/acsenergylett.2c00326
摘要
Metallic bismuth (Bi) shows great promise in electrocatalytic CO2 reduction into formate. However, the direct synthesis of active and stable Bi electrocatalysts remains a grand challenge. Herein, we present an in-plane confined hydrogen-reduction strategy for in situ growth of edge-modified Bi nanoribbons, which enables enhanced and stable reduction of CO2 into formate. Density functional theory calculations suggest that the synergistic effect of a preferentially exposed (113) facet and abundant Bi–O edge sites can contribute to a reduced formation energy for the formate intermediate. Moreover, in situ Raman characterizations reveal the Bi–O edge sites can remain stable during the reaction. Consequently, the Bi nanoribbons exhibit a high formate Faradaic efficiency of over 95% in a wide potential window. More impressively, a negligible degradation in selectivity and activity after more than 100 h of continuous operation can be achieved. This work provides a feasible strategy for fabricating robust catalysts for efficient CO2 reduction.
科研通智能强力驱动
Strongly Powered by AbleSci AI