TY - JOUR
T1 - Atomically dispersed Ni(i) as the active site for electrochemical CO2 reduction
AU - Yang, Hong Bin
AU - Hung, Sung-Fu
AU - Liu, Song
AU - Yuan, Kaidi
AU - Miao, Shu
AU - Zhang, Liping
AU - Huang, Xiang
AU - Wang, Hsin-Yi
AU - Cai, Weizheng
AU - Chen, Rong
AU - Gao, Jiajian
AU - Yang, Xiaofeng
AU - Chen, Wei
AU - Huang, Yanqiang
AU - Chen, Hao Ming
AU - Li, Chang Ming
AU - Zhang, Tao
AU - Liu, Bin
N1 - Publication details (e.g. title, author(s), publication statuses and dates) are captured on an “AS IS” and “AS AVAILABLE” basis at the time of record harvesting from the data source. Suggestions for further amendments or supplementary information can be sent to [email protected].
PY - 2018/2/1
Y1 - 2018/2/1
N2 - Electrochemical reduction of CO2 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 CO2 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 CO2 reduction activity, reaching a specific current of 350 A gcatalyst -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. © 2018 The Author(s).
AB - Electrochemical reduction of CO2 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 CO2 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 CO2 reduction activity, reaching a specific current of 350 A gcatalyst -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. © 2018 The Author(s).
UR - https://www.scopus.com/pages/publications/85041693198
UR - https://www.scopus.com/record/pubmetrics.uri?eid=2-s2.0-85041693198&origin=recordpage
U2 - 10.1038/s41560-017-0078-8
DO - 10.1038/s41560-017-0078-8
M3 - RGC 21 - Publication in refereed journal
SN - 2058-7546
VL - 3
SP - 140
EP - 147
JO - Nature Energy
JF - Nature Energy
IS - 2
ER -