Atomically dispersed Ni(i) as the active site for electrochemical CO2 reduction

Electrochemical reduction of CO 2 to chemical fuel offers a promising strategy for managing the global carbon balance, but presents challenges for chemistry due to the lack of effective electrocatalyst. Here we report atomically dispersed nickel on nitrogenated graphene as an efficient and durable e...

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Veröffentlicht in:Nature energy 2018-02, Vol.3 (2), p.140-147
Hauptverfasser: Yang, Hong Bin, Hung, Sung-Fu, Liu, Song, Yuan, Kaidi, Miao, Shu, Zhang, Liping, Huang, Xiang, Wang, Hsin-Yi, Cai, Weizheng, Chen, Rong, Gao, Jiajian, Yang, Xiaofeng, Chen, Wei, Huang, Yanqiang, Chen, Hao Ming, Li, Chang Ming, Zhang, Tao, Liu, Bin
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Sprache:eng
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Zusammenfassung:Electrochemical reduction of CO 2 to chemical fuel offers a promising strategy for managing the global carbon balance, but presents challenges for chemistry due to the lack of effective electrocatalyst. Here we report atomically dispersed nickel on nitrogenated graphene as an efficient and durable electrocatalyst for CO 2 reduction. Based on operando X-ray absorption and photoelectron spectroscopy measurements, the monovalent Ni( i ) atomic center with a d 9 electronic configuration was identified as the catalytically active site. The single-Ni-atom catalyst exhibits high intrinsic CO 2 reduction activity, reaching a specific current of 350 A g catalyst −1 and turnover frequency of 14,800 h −1 at a mild overpotential of 0.61 V for CO conversion with 97% Faradaic efficiency. The catalyst maintained 98% of its initial activity after 100 h of continuous reaction at CO formation current densities as high as 22 mA cm −2 . Electrocatalysts with improved activity and stability for the conversion of CO 2 to CO are being sought. Using operando spectroscopies, the authors identify atomically dispersed Ni( i ) as the active site in a nitrogenated-graphene-supported catalyst with high intrinsic activity and stability over 100 hours.
ISSN:2058-7546
2058-7546
DOI:10.1038/s41560-017-0078-8