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Steering surface reconstruction of copper with electrolyte additives for CO(2) electroreduction

Electrocatalytic CO(2) reduction to value-added hydrocarbon products using metallic copper (Cu) catalysts is a potentially sustainable approach to facilitate carbon neutrality. However, Cu metal suffers from unavoidable and uncontrollable surface reconstruction during electrocatalysis, which can hav...

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Detalles Bibliográficos
Autores principales: Han, Zishan, Han, Daliang, Chen, Zhe, Gao, Jiachen, Jiang, Guangyi, Wang, Xinyu, Lyu, Shuaishuai, Guo, Yong, Geng, Chuannan, Yin, Lichang, Weng, Zhe, Yang, Quan-Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9174297/
https://www.ncbi.nlm.nih.gov/pubmed/35672315
http://dx.doi.org/10.1038/s41467-022-30819-1
Descripción
Sumario:Electrocatalytic CO(2) reduction to value-added hydrocarbon products using metallic copper (Cu) catalysts is a potentially sustainable approach to facilitate carbon neutrality. However, Cu metal suffers from unavoidable and uncontrollable surface reconstruction during electrocatalysis, which can have either adverse or beneficial effects on its electrocatalytic performance. In a break from the current catalyst design path, we propose a strategy guiding the reconstruction process in a favorable direction to improve the performance. Typically, the controlled surface reconstruction is facilely realized using an electrolyte additive, ethylenediamine tetramethylenephosphonic acid, to substantially promote CO(2) electroreduction to CH(4) for commercial polycrystalline Cu. As a result, a stable CH(4) Faradaic efficiency of 64% with a partial current density of 192 mA cm(−2), thus enabling an impressive CO(2)-to-CH(4) conversion rate of 0.25 µmol cm(−2) s(−1), is achieved in an alkaline flow cell. We believe our study will promote the exploration of electrochemical reconstruction and provide a promising route for the discovery of high-performance electrocatalysts.