Ionic Liquid‐Induced Product Switching in CO2 Electroreduction on Copper Reaction Interface

The electrochemical reduction of CO2 (CO2RR) mainly occurs at the three‐phase interface, and the properties of an interface can directly affect the CO2RR pathway. Cu‐based materials can produce considerable amounts of alcohols and hydrocarbons, but it is hard to precisely regulate the reaction inter...

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Veröffentlicht in:Advanced functional materials 2024-10, Vol.34 (41), p.n/a
Hauptverfasser: Cai, Huizhu, Yang, Hengpan, Feng, Jianpeng, Zhou, Kangjie, Liu, Changsha, Hu, Qi, He, Chuanxin
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Sprache:eng
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Zusammenfassung:The electrochemical reduction of CO2 (CO2RR) mainly occurs at the three‐phase interface, and the properties of an interface can directly affect the CO2RR pathway. Cu‐based materials can produce considerable amounts of alcohols and hydrocarbons, but it is hard to precisely regulate the reaction interface and obtain specific target products. Herein, the properties of the Cu surface through a facile strategy of ionic liquid modification are successfully adjusted. According to theoretical calculations and in situ Raman and FTIR spectra characterizations, it is revealed that the introduction of ionic liquids (e.g., [Bmim][PF6]) can control the energy barriers and distribution density of key intermediates on Cu interface, thus totally change the reaction pathway of CO2 electroreduction. Consequently, the dominant products from the Cu catalyst will be dramatically switched between C2H4 with a 71.1% Faraday efficiency (FE) and CH4 with a 67.2% FE. It is rarely seen in previous reports that the CO2RR products can be fundamentally changed through simple interface modifications. This work offers a straightforward approach to tune the interfacial properties and understand the mechanisms in various electrocatalytic reactions. A facile strategy of ionic‐liquid modification is proposed to regulate the surface of the Cu catalyst, which can totally change the reaction pathways and realize the product switching between C2H4 and CH4 in CO2 electroreduction.
ISSN:1616-301X
1616-3028
DOI:10.1002/adfm.202404102