Ultrafine dual‐phased carbide nanocrystals confined in porous nitrogen‐doped carbon dodecahedrons for efficient hydrogen evolution reaction

Designing novel non-noble electrocatalysts with controlled structures and composition remains a great challenge for efficient hydrogen evolution reaction (HER). Herein, a rational synthesis of ultrafine carbide nanocrystals confined in porous nitrogen-doped carbon dodecahedrons (PNCDs) by annealing...

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Main Authors: Lu, Xue Feng, Yu, Le, Zhang, Jintao, Lou, David Xiong Wen
Other Authors: School of Chemical and Biomedical Engineering
Format: Article
Language:English
Published: 2020
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Online Access:https://hdl.handle.net/10356/138565
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1385652023-12-29T06:48:38Z Ultrafine dual‐phased carbide nanocrystals confined in porous nitrogen‐doped carbon dodecahedrons for efficient hydrogen evolution reaction Lu, Xue Feng Yu, Le Zhang, Jintao Lou, David Xiong Wen School of Chemical and Biomedical Engineering Engineering::Chemical engineering Dual-phased Carbides Designing novel non-noble electrocatalysts with controlled structures and composition remains a great challenge for efficient hydrogen evolution reaction (HER). Herein, a rational synthesis of ultrafine carbide nanocrystals confined in porous nitrogen-doped carbon dodecahedrons (PNCDs) by annealing functional zeolitic imidazolate framework (ZIF-8) with molybdate or tungstate is reported. By controlling the substitution amount of MO4 units (M = Mo or W) in the ZIF-8 framework, dual-phase carbide nanocrystals confined in PNCDs (denoted as MC-M2 C/PNCDs) can be obtained, which exhibit superior activity toward the HER to the single-phased MC/PNCDs and M2 C/PNCDs. The evenly distributed ultrafine nanocrystals favor the exposure of active sites. PNCDs as the support facilitate charge transfer and protect the nanocrystals from aggregation during the HER process. Moreover, the strong coupling interactions between MC and M2 C provide beneficial sites for both water dissociation and hydrogen desorption. This work highlights a new feasible strategy to explore efficient electrocatalysts via engineering on nanostructure and composition. NRF (Natl Research Foundation, S’pore) MOE (Min. of Education, S’pore) Accepted version 2020-05-08T06:12:21Z 2020-05-08T06:12:21Z 2019 Journal Article Lu, X. F., Yu, L., Zhang, J., & Lou, D. X. W. (2019). Ultrafine dual‐phased carbide nanocrystals confined in porous nitrogen‐doped carbon dodecahedrons for efficient hydrogen evolution reaction. Advanced Materials, 31(30), 1900699-. doi:10.1002/adma.201900699 0935-9648 https://hdl.handle.net/10356/138565 10.1002/adma.201900699 31168857 2-s2.0-85067601878 30 31 1900699 (1 of 8) 1900699 (8 of 8) en Advanced Materials © 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. All rights reserved. This paper was published in Advanced Materials and is made available with permission of WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. 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
Dual-phased
Carbides
spellingShingle Engineering::Chemical engineering
Dual-phased
Carbides
Lu, Xue Feng
Yu, Le
Zhang, Jintao
Lou, David Xiong Wen
Ultrafine dual‐phased carbide nanocrystals confined in porous nitrogen‐doped carbon dodecahedrons for efficient hydrogen evolution reaction
description Designing novel non-noble electrocatalysts with controlled structures and composition remains a great challenge for efficient hydrogen evolution reaction (HER). Herein, a rational synthesis of ultrafine carbide nanocrystals confined in porous nitrogen-doped carbon dodecahedrons (PNCDs) by annealing functional zeolitic imidazolate framework (ZIF-8) with molybdate or tungstate is reported. By controlling the substitution amount of MO4 units (M = Mo or W) in the ZIF-8 framework, dual-phase carbide nanocrystals confined in PNCDs (denoted as MC-M2 C/PNCDs) can be obtained, which exhibit superior activity toward the HER to the single-phased MC/PNCDs and M2 C/PNCDs. The evenly distributed ultrafine nanocrystals favor the exposure of active sites. PNCDs as the support facilitate charge transfer and protect the nanocrystals from aggregation during the HER process. Moreover, the strong coupling interactions between MC and M2 C provide beneficial sites for both water dissociation and hydrogen desorption. This work highlights a new feasible strategy to explore efficient electrocatalysts via engineering on nanostructure and composition.
author2 School of Chemical and Biomedical Engineering
author_facet School of Chemical and Biomedical Engineering
Lu, Xue Feng
Yu, Le
Zhang, Jintao
Lou, David Xiong Wen
format Article
author Lu, Xue Feng
Yu, Le
Zhang, Jintao
Lou, David Xiong Wen
author_sort Lu, Xue Feng
title Ultrafine dual‐phased carbide nanocrystals confined in porous nitrogen‐doped carbon dodecahedrons for efficient hydrogen evolution reaction
title_short Ultrafine dual‐phased carbide nanocrystals confined in porous nitrogen‐doped carbon dodecahedrons for efficient hydrogen evolution reaction
title_full Ultrafine dual‐phased carbide nanocrystals confined in porous nitrogen‐doped carbon dodecahedrons for efficient hydrogen evolution reaction
title_fullStr Ultrafine dual‐phased carbide nanocrystals confined in porous nitrogen‐doped carbon dodecahedrons for efficient hydrogen evolution reaction
title_full_unstemmed Ultrafine dual‐phased carbide nanocrystals confined in porous nitrogen‐doped carbon dodecahedrons for efficient hydrogen evolution reaction
title_sort ultrafine dual‐phased carbide nanocrystals confined in porous nitrogen‐doped carbon dodecahedrons for efficient hydrogen evolution reaction
publishDate 2020
url https://hdl.handle.net/10356/138565
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