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Nanostructured Au Electrode with 100 h Stability for Solar-Driven Electrochemical Reduction of Carbon Dioxide to Carbon Monoxide

[Image: see text] Solar-to-chemical energy conversion is a potential alternative to fossil fuels. A promising approach is the electrochemical (EC) reduction of CO(2) to value-added chemicals, particularly hydrocarbons. Here, we report on the selective EC reduction of CO(2) to CO on a porous Au nanos...

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Detalles Bibliográficos
Autores principales: Bae, Hyojung, Seong, Chaewon, Burungale, Vishal, Seol, Myeongheon, Yoon, Chul Oh, Kang, Soon Hyung, Jung, Wan-Gil, Kim, Bong-Joong, Ha, Jun-Seok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8945059/
https://www.ncbi.nlm.nih.gov/pubmed/35350324
http://dx.doi.org/10.1021/acsomega.1c06720
Descripción
Sumario:[Image: see text] Solar-to-chemical energy conversion is a potential alternative to fossil fuels. A promising approach is the electrochemical (EC) reduction of CO(2) to value-added chemicals, particularly hydrocarbons. Here, we report on the selective EC reduction of CO(2) to CO on a porous Au nanostructure (pAu) cathode in 0.1 M KHCO(3). The pAu cathode anodized at 2.6 V exhibited maximum Faradaic efficiency (FE) for conversion of CO(2) to CO (up to 100% at −0.75 V vs reversible hydrogen electrode (RHE)). Furthermore, commercial Si photovoltaic cells were combined with EC systems (PV-EC) consisting of pAu cathodes and IrO(2) anodes. The triple-junction cell and EC system resulted in a solar-to-CO conversion efficiency (SCE) of 5.3% under 1 sun illumination and was operated for 100 h. This study provides a PV-EC CO(2) reduction system for CO production and indicates the potential of the PV-EC system for the EC reduction of CO(2) to value-added chemicals.