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Phosphorus‐Doped Graphene Aerogel as Self‐Supported Electrocatalyst for CO(2)‐to‐Ethanol Conversion

Electrochemical reduction of carbon dioxide (CO(2)) to ethanol is a promising strategy for global warming mitigation and resource utilization. However, due to the intricacy of C─C coupling and multiple proton–electron transfers, CO(2)‐to‐ethanol conversion remains a great challenge with low activity...

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Detalles Bibliográficos
Autores principales: Yang, Fangqi, Liang, Caihong, Yu, Haoming, Zeng, Zheling, Lam, Yeng Ming, Deng, Shuguang, Wang, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9443446/
https://www.ncbi.nlm.nih.gov/pubmed/35821388
http://dx.doi.org/10.1002/advs.202202006
Descripción
Sumario:Electrochemical reduction of carbon dioxide (CO(2)) to ethanol is a promising strategy for global warming mitigation and resource utilization. However, due to the intricacy of C─C coupling and multiple proton–electron transfers, CO(2)‐to‐ethanol conversion remains a great challenge with low activity and selectivity. Herein, it is reported a P‐doped graphene aerogel as a self‐supporting electrocatalyst for CO(2) reduction to ethanol. High ethanol Faradaic efficiency (FE) of 48.7% and long stability of 70 h are achieved at −0.8 V(RHE). Meanwhile, an outstanding ethanol yield of 14.62 µmol h(−1) cm(−2) can be obtained, outperforming most reported electrocatalysts. In situ Raman spectra indicate the important role of adsorbed *CO intermediates in CO(2)‐to‐ethanol conversion. Furthermore, the possible active sites and optimal pathway for ethanol formation are revealed by density functional theory calculations. The graphene zigzag edges with P doping enhance the adsorption of *CO intermediate and increase the coverage of *CO on the catalyst surface, which facilitates the *CO dimerization and boosts the EtOH formation. In addition, the hierarchical pore structure of P‐doped graphene aerogels exposes abundant active sites and facilitates mass/charge transfer. This work provides inventive insight into designing metal‐free catalysts for liquid products from CO(2) electroreduction.