格式化
催化作用
甲酸
电化学
金属有机骨架
配体(生物化学)
二氧化碳电化学还原
材料科学
可逆氢电极
铋
电催化剂
吸附
化学工程
无机化学
电极
化学
有机化学
工作电极
一氧化碳
物理化学
生物化学
受体
工程类
冶金
作者
Nanhui Li,Ping Yan,Yuanhao Tang,Sheng Wang,Xin‐Yao Yu,Hao Bin Wu
标识
DOI:10.1016/j.apcatb.2021.120481
摘要
Electrochemical reduction of carbon dioxide provides a feasible solution to the energy and climate crisis. Bi-based catalysts are promising candidates to electrochemically convert carbon dioxide (CO2) into formic acid or formate. Herein, ligand-stabilized Bi nanosheets are obtained from in-situ electrochemical reduction of a Bi-based metal-organic framework, which exhibit remarkable electrocatalytic performance for CO2 reduction. A high Faradic efficiency of 98 % for formate is achieved at a potential of -0.80 V vs. reversible hydrogen electrode (RHE) with an improved durability over 40 h. The remarkable electrocatalytic activity and stability could be attributed to the in-situ generated catalyst with abundant under-coordinated Bi active sites, which are effectively stabilized by residual ligands adsorbed on surface. This study demonstrates that ligand-stabilized under-coordinated surface sites would be facilely generated from in-situ transformation of metal-organic precursors for highly efficient CO2 conversion.
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