电催化剂
催化作用
碳纤维
还原(数学)
氧还原反应
化学
材料科学
纳米技术
化学工程
电化学
电极
物理化学
有机化学
工程类
复合数
数学
复合材料
几何学
作者
Hao Wan,Yan Jiao,Alexander Bagger,Jan Rossmeisl
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2020-12-28
卷期号:11 (2): 533-541
被引量:47
标识
DOI:10.1021/acscatal.0c04878
摘要
A challenge in the electrochemical CO2 reduction reaction (CO2RR) is the lack of efficient and selective electrocatalysts to valuable chemicals. Hydrocarbons and valuable chemicals from the CO2RR have primarily been observed on metallic Cu. Here, 3D carbon electrocatalysts (diporphyrin molecules; i.e., Pacman) have been investigated as potential CO2RR electrocatalysts using density functional theory simulations. This work presents a molecular-level engineering strategy for the development of electrocatalysts toward hydrocarbons. The introduction of a second metal center in the diporphyrins on one hand serves as a proton transfer or CO adsorption site, providing the possibility for the formation of C–H and C–C bonds. On the other hand, the second metal center selectively stabilizes key intermediates like *CH2O, *OCH3, and *OCCHOH, leading to CH4 and C2 species production. It has been found that Pacman (Pac) with Mn or Fe is able to produce CH4. Furthermore, Pac-CoNi, Pac-CoCu, and Pac-CoCo with pyridine coordination catalysts generate CH3OH, while Pac-CoCo might enable C–C coupling, forming C2 species.
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