Loading single-Ni atoms on assembled hollow N-rich carbon plates for efficient CO₂ electroreduction

The rational design of catalysts' spatial structure is vitally important to boost catalytic performance through exposing the active sites, enhancing the mass transfer, and confining the reactants. Herein, a dual-linker zeolitic tetrazolate framework-engaged strategy is developed to construct as...

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Main Authors: Li, Yunxiang, Zhang, Song Lin, Cheng, Weiren, Chen, Ye, Luan, Deyan, Gao, Shuyan, Lou, David Xiong Wen
Other Authors: School of Chemical and Biomedical Engineering
Format: Article
Language:English
Published: 2022
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Online Access:https://hdl.handle.net/10356/156848
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1568482023-12-29T06:49:21Z Loading single-Ni atoms on assembled hollow N-rich carbon plates for efficient CO₂ electroreduction Li, Yunxiang Zhang, Song Lin Cheng, Weiren Chen, Ye Luan, Deyan Gao, Shuyan Lou, David Xiong Wen School of Chemical and Biomedical Engineering Engineering::Chemical engineering Electrocatalysis Hollow Carbon The rational design of catalysts' spatial structure is vitally important to boost catalytic performance through exposing the active sites, enhancing the mass transfer, and confining the reactants. Herein, a dual-linker zeolitic tetrazolate framework-engaged strategy is developed to construct assembled hollow plates (AHP) of N-rich carbon (NC), which is loaded with single-Ni atoms to form a highly efficient electrocatalyst (designated as Ni-NC(AHP)). In the carbonization process, the thermally unstable linker (5-aminotetrazole) serves as the self-sacrificial template and the other linker (2-methylimidazole) mainly serves as the carbon and nitrogen source to form hollow NC matrix. The formed Ni-NC(AHP) catalyst possesses enhanced mesoporosity and more available surface area, thus promoting mass transport and affording abundant accessible single-Ni sites. These features contribute to remarkable performance for electrochemical CO2 reduction with exceptionally high selectivity of nearly 100% towards CO in a wide potential range and dramatically enhanced CO partial current density. Ministry of Education (MOE) Submitted/Accepted version X.W.L. acknowledges the funding support from the Ministry of Education of Singapore through the Academic Research Fund (AcRF) Tier-2 grants (MOE2017-T2-2-003; MOE2019-T2-2-049). 2022-04-27T05:59:27Z 2022-04-27T05:59:27Z 2022 Journal Article Li, Y., Zhang, S. L., Cheng, W., Chen, Y., Luan, D., Gao, S. & Lou, D. X. W. (2022). Loading single-Ni atoms on assembled hollow N-rich carbon plates for efficient CO₂ electroreduction. Advanced Materials, 34(1), 2105204-. https://dx.doi.org/10.1002/adma.202105204 0935-9648 https://hdl.handle.net/10356/156848 10.1002/adma.202105204 34610187 2-s2.0-85117469588 1 34 2105204 en MOE2017-T2-2-0039 MOE2019-T2-2-04 Advanced Materials This is the peer reviewed version of the following article: Li, Y., Zhang, S. L., Cheng, W., Chen, Y., Luan, D., Gao, S. & Lou, D. X. W. (2022). Loading single-Ni atoms on assembled hollow N-rich carbon plates for efficient CO₂ electroreduction. Advanced Materials, 34(1), 2105204-, which has been published in final form at https://doi.org/10.1002/adma.202105204. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Engineering::Chemical engineering
Electrocatalysis
Hollow Carbon
spellingShingle Engineering::Chemical engineering
Electrocatalysis
Hollow Carbon
Li, Yunxiang
Zhang, Song Lin
Cheng, Weiren
Chen, Ye
Luan, Deyan
Gao, Shuyan
Lou, David Xiong Wen
Loading single-Ni atoms on assembled hollow N-rich carbon plates for efficient CO₂ electroreduction
description The rational design of catalysts' spatial structure is vitally important to boost catalytic performance through exposing the active sites, enhancing the mass transfer, and confining the reactants. Herein, a dual-linker zeolitic tetrazolate framework-engaged strategy is developed to construct assembled hollow plates (AHP) of N-rich carbon (NC), which is loaded with single-Ni atoms to form a highly efficient electrocatalyst (designated as Ni-NC(AHP)). In the carbonization process, the thermally unstable linker (5-aminotetrazole) serves as the self-sacrificial template and the other linker (2-methylimidazole) mainly serves as the carbon and nitrogen source to form hollow NC matrix. The formed Ni-NC(AHP) catalyst possesses enhanced mesoporosity and more available surface area, thus promoting mass transport and affording abundant accessible single-Ni sites. These features contribute to remarkable performance for electrochemical CO2 reduction with exceptionally high selectivity of nearly 100% towards CO in a wide potential range and dramatically enhanced CO partial current density.
author2 School of Chemical and Biomedical Engineering
author_facet School of Chemical and Biomedical Engineering
Li, Yunxiang
Zhang, Song Lin
Cheng, Weiren
Chen, Ye
Luan, Deyan
Gao, Shuyan
Lou, David Xiong Wen
format Article
author Li, Yunxiang
Zhang, Song Lin
Cheng, Weiren
Chen, Ye
Luan, Deyan
Gao, Shuyan
Lou, David Xiong Wen
author_sort Li, Yunxiang
title Loading single-Ni atoms on assembled hollow N-rich carbon plates for efficient CO₂ electroreduction
title_short Loading single-Ni atoms on assembled hollow N-rich carbon plates for efficient CO₂ electroreduction
title_full Loading single-Ni atoms on assembled hollow N-rich carbon plates for efficient CO₂ electroreduction
title_fullStr Loading single-Ni atoms on assembled hollow N-rich carbon plates for efficient CO₂ electroreduction
title_full_unstemmed Loading single-Ni atoms on assembled hollow N-rich carbon plates for efficient CO₂ electroreduction
title_sort loading single-ni atoms on assembled hollow n-rich carbon plates for efficient co₂ electroreduction
publishDate 2022
url https://hdl.handle.net/10356/156848
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