格式化
电催化剂
金属间化合物
催化作用
法拉第效率
化学
甲酸甲酯
选择性
材料科学
可逆氢电极
无机化学
化学工程
电化学
物理化学
冶金
电极
有机化学
合金
参比电极
工程类
作者
Linfeng Xie,Xuan Liu,Fanyang Huang,Jiashun Liang,Jianyun Liu,Tanyuan Wang,Li‐Ming Yang,Ruiguo Cao,Qing Li
标识
DOI:10.1016/s1872-2067(21)63999-2
摘要
Electrocatalytic CO2 reduction plays an important role in the reduction of the CO2 concentration in atmosphere and consequently the mitigation of greenhouse effects. Pd has been extensively investigated as an electrocatalyst for the CO2 reduction to formate, which is an important raw material in the production of organic chemicals. However, the low selectivity and competitive reaction (hydrogen evolution reaction (HER)) have hindered the performance of monometallic Pd catalysts. In this paper, intermetallic PdBi nanosheets (NSs) are prepared for efficient CO2 reduction to formate. The highest Faradaic efficiency (FE) of formate on fully ordered PdBi NSs reaches 91.9% at −1.0 V vs. RHE, which outperforms that of the disordered PdBi and pure Pd catalysts. Density functional theory calculations suggest that compared to disordered PdBi NSs, the ordered structure can decrease the free energy barrier of *OCHO (a key intermediate of formate formation) and inhibit H2 evolution as well, thereby enhancing the activity and selectivity for formate production.
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