Cargando…

Copper-on-nitride enhances the stable electrosynthesis of multi-carbon products from CO(2)

Copper-based materials are promising electrocatalysts for CO(2) reduction. Prior studies show that the mixture of copper (I) and copper (0) at the catalyst surface enhances multi-carbon products from CO(2) reduction; however, the stable presence of copper (I) remains the subject of debate. Here we r...

Descripción completa

Detalles Bibliográficos
Autores principales: Liang, Zhi-Qin, Zhuang, Tao-Tao, Seifitokaldani, Ali, Li, Jun, Huang, Chun-Wei, Tan, Chih-Shan, Li, Yi, De Luna, Phil, Dinh, Cao Thang, Hu, Yongfeng, Xiao, Qunfeng, Hsieh, Pei-Lun, Wang, Yuhang, Li, Fengwang, Quintero-Bermudez, Rafael, Zhou, Yansong, Chen, Peining, Pang, Yuanjie, Lo, Shen-Chuan, Chen, Lih-Juann, Tan, Hairen, Xu, Zheng, Zhao, Suling, Sinton, David, Sargent, Edward H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6148248/
https://www.ncbi.nlm.nih.gov/pubmed/30237471
http://dx.doi.org/10.1038/s41467-018-06311-0
Descripción
Sumario:Copper-based materials are promising electrocatalysts for CO(2) reduction. Prior studies show that the mixture of copper (I) and copper (0) at the catalyst surface enhances multi-carbon products from CO(2) reduction; however, the stable presence of copper (I) remains the subject of debate. Here we report a copper on copper (I) composite that stabilizes copper (I) during CO(2) reduction through the use of copper nitride as an underlying copper (I) species. We synthesize a copper-on-nitride catalyst that exhibits a Faradaic efficiency of 64 ± 2% for C(2+) products. We achieve a 40-fold enhancement in the ratio of C(2+) to the competing CH(4) compared to the case of pure copper. We further show that the copper-on-nitride catalyst performs stable CO(2) reduction over 30 h. Mechanistic studies suggest that the use of copper nitride contributes to reducing the CO dimerization energy barrier—a rate-limiting step in CO(2) reduction to multi-carbon products.