法拉第效率
材料科学
电化学
催化作用
微型多孔材料
铜
无机化学
吸附
沸石
化学工程
氧化还原
碳酸盐
电催化剂
固态
燃料电池
多相催化
电极
氧化态
反应机理
过渡金属
作者
Yingying Jin,Jiong Wang
标识
DOI:10.1021/acsami.5c22306
摘要
Electrochemical CO2 reduction reaction (CO2R) in acidic media represents a promising route to CO2 utilization by circumventing the critical concern of carbonate formation in water. Herein, we report that silicalite-1 (S-1) zeolites functioned as a solid support for copper oxides (CuO), which demonstrated superior performance in electrochemical CO2 conversion into hydrocarbons in acidic media. The as-derived catalyst achieved a Faradaic efficiency (FE) above 40% for the production of CH4 and C2H4 at relatively high overpotentials. Systematic control experiments revealed that the microporosity of S-1 zeolite concentrated CO2 through its high physical adsorption ability, while the silica surface stabilized the Cu oxidation state against an extreme reduction environment. Such effects enabled selective and durable CO2 conversion. These results underscore the potential of microporous zeolites as an efficient support for designing high-performance CO2R electrocatalysts.
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