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

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 el...

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Main Authors: 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
Other Authors: School of Chemical and Biomedical Engineering
Format: Article
Language:English
Published: 2020
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Online Access:https://hdl.handle.net/10356/140498
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1404982020-05-29T08:52:27Z Atomically dispersed Ni(I) as the active site for electrochemical CO2 reduction 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 School of Chemical and Biomedical Engineering Engineering::Chemical engineering Carbon Capture and Storage Electrocatalysis 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 d9 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. NRF (Natl Research Foundation, S’pore) ASTAR (Agency for Sci., Tech. and Research, S’pore) MOE (Min. of Education, S’pore) 2020-05-29T08:52:26Z 2020-05-29T08:52:26Z 2018 Journal Article Yang, H. B., Hung, S.-F., Liu, S., Yuan, K., Miao, S., Zhang, L., . . . Liu, B. (2018). Atomically dispersed Ni(I) as the active site for electrochemical CO2 reduction. Nature Energy, 3(2), 140-147. doi:10.1038/s41560-017-0078-8 2058-7546 https://hdl.handle.net/10356/140498 10.1038/s41560-017-0078-8 2-s2.0-85041693198 2 3 140 147 en Nature Energy © 2018 Macmillan Publishers Limited, part of Springer Nature. All rights reserved.
institution Nanyang Technological University
building NTU Library
country Singapore
collection DR-NTU
language English
topic Engineering::Chemical engineering
Carbon Capture and Storage
Electrocatalysis
spellingShingle Engineering::Chemical engineering
Carbon Capture and Storage
Electrocatalysis
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
Atomically dispersed Ni(I) as the active site for electrochemical CO2 reduction
description 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 d9 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.
author2 School of Chemical and Biomedical Engineering
author_facet School of Chemical and Biomedical Engineering
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
format Article
author 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
author_sort Yang, Hong Bin
title Atomically dispersed Ni(I) as the active site for electrochemical CO2 reduction
title_short Atomically dispersed Ni(I) as the active site for electrochemical CO2 reduction
title_full Atomically dispersed Ni(I) as the active site for electrochemical CO2 reduction
title_fullStr Atomically dispersed Ni(I) as the active site for electrochemical CO2 reduction
title_full_unstemmed Atomically dispersed Ni(I) as the active site for electrochemical CO2 reduction
title_sort atomically dispersed ni(i) as the active site for electrochemical co2 reduction
publishDate 2020
url https://hdl.handle.net/10356/140498
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