双金属片
化学
催化作用
甲酸
无机化学
格式化
铋
电化学
氧化物
金属有机骨架
法拉第效率
二氧化碳电化学还原
纳米颗粒
煅烧
碳纤维
选择性
电催化剂
化学工程
电极
一氧化碳
有机化学
材料科学
物理化学
吸附
复合材料
复合数
工程类
作者
Qinru Wang,Xiaofeng Yang,Hu Zang,Feiran Chen,Chao Wang,Nan Ye,Baoyou Geng
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2022-07-15
卷期号:61 (30): 12003-12011
被引量:24
标识
DOI:10.1021/acs.inorgchem.2c01961
摘要
Bismuth-based catalysts exhibit excellent activity and selectivity for the electroreduction of carbon dioxide (CO2). However, single-component bismuth-based catalysts are not satisfactory for the electrochemical reduction of CO2 to formic acid, mainly due to their high hydrogen production, low electrical conductivity, and small catalytic current density. Herein, we used a coordination strategy to recombine Bi and In at the molecular level to form Bi/In bimetallic metal-organic frameworks (MOFs), which were then calcined to obtain MOF-derived Bi/In bimetallic oxide nanoparticles embedded in carbon networks. Thanks to the synergistic effect of bimetallic components, high specific surface area, suitable pore size distribution, and high electrical conductivity of the carbon network, the material exhibits excellent activity and selectivity for electroreduction of CO2 to formate. In H-type electrolyzers, the formate Faradaic efficiency reaches 91% at -0.9 V (vs RHE) and does not decrease significantly within 48 h. In situ Fourier transform infrared spectroscopy confirms the reaction intermediates and reveals that CO2 electroreduction is dominant by the *OCHO pathway.
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