Ultrafine molybdenum carbide nanocrystals confined in carbon foams via a colloid-confinement route for efficient hydrogen production

Precise size‐controlled synthesis and multiscale assembly of ultrafine non‐noble‐metal‐based catalysts play a key role in electrochemical energy conversion. Herein, a novel colloid‐confinement strategy for facile synthesis of ultrafine molybdenum carbide nanocrystals with sub‐2 nm average size assem...

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Main Authors: Kou, Zongkui, Wang, Tingting, Cai, Yi, Guan, Cao, Pu, Zonghua, Zhu, Changrong, Hu, Yating, Elshahawy, Abdelnaby M., Wang, John, Mu, Shichun
Other Authors: School of Materials Science & Engineering
Format: Article
Language:English
Published: 2020
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Online Access:https://hdl.handle.net/10356/138469
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1384692020-06-01T10:26:45Z Ultrafine molybdenum carbide nanocrystals confined in carbon foams via a colloid-confinement route for efficient hydrogen production Kou, Zongkui Wang, Tingting Cai, Yi Guan, Cao Pu, Zonghua Zhu, Changrong Hu, Yating Elshahawy, Abdelnaby M. Wang, John Mu, Shichun School of Materials Science & Engineering Engineering::Materials Colloid Confinement Hydrogen Evolution Reaction Precise size‐controlled synthesis and multiscale assembly of ultrafine non‐noble‐metal‐based catalysts play a key role in electrochemical energy conversion. Herein, a novel colloid‐confinement strategy for facile synthesis of ultrafine molybdenum carbide nanocrystals with sub‐2 nm average size assembled in carbon foams (uf‐Mo2C/CF) is reported. First, uniformly sized colloidal SiO2 nanospheres are chosen to confine the metal source (NH4)6Mo7O24 molecules and the glucose is as carbon source. Subsequently, by a high temperature reduction–carbonization, Mo2C nanocrystals are achieved and uniformly assembled on the in situ formed amorphous carbon foams. The as formed uf‐Mo2C/CF demonstrates superior hydrogen evolution activity and outstanding stability in the whole pH range. These results indicate the validity of size control and multiscale structural assembly of metal carbide nanocrystals by consideration of the overall mass transport, accessibility, and quantity, as well as the capability of the active sites toward efficient electrocatalytic hydrogen evolution reaction. This strategy can also be expanded to other energy‐related application. MOE (Min. of Education, S’pore) 2020-05-06T08:39:10Z 2020-05-06T08:39:10Z 2018 Journal Article Kou, Z., Wang, T., Cai, Y., Guan, C., Pu, Z., Zhu, C., . . . Mu, S. (2018). Ultrafine molybdenum carbide nanocrystals confined in carbon foams via a colloid-confinement route for efficient hydrogen production. Small Methods, 2(4), 1700396-. doi:10.1002/smtd.201700396 2366-9608 https://hdl.handle.net/10356/138469 10.1002/smtd.201700396 4 2 en Small Methods © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. All rights reserved.
institution Nanyang Technological University
building NTU Library
country Singapore
collection DR-NTU
language English
topic Engineering::Materials
Colloid Confinement
Hydrogen Evolution Reaction
spellingShingle Engineering::Materials
Colloid Confinement
Hydrogen Evolution Reaction
Kou, Zongkui
Wang, Tingting
Cai, Yi
Guan, Cao
Pu, Zonghua
Zhu, Changrong
Hu, Yating
Elshahawy, Abdelnaby M.
Wang, John
Mu, Shichun
Ultrafine molybdenum carbide nanocrystals confined in carbon foams via a colloid-confinement route for efficient hydrogen production
description Precise size‐controlled synthesis and multiscale assembly of ultrafine non‐noble‐metal‐based catalysts play a key role in electrochemical energy conversion. Herein, a novel colloid‐confinement strategy for facile synthesis of ultrafine molybdenum carbide nanocrystals with sub‐2 nm average size assembled in carbon foams (uf‐Mo2C/CF) is reported. First, uniformly sized colloidal SiO2 nanospheres are chosen to confine the metal source (NH4)6Mo7O24 molecules and the glucose is as carbon source. Subsequently, by a high temperature reduction–carbonization, Mo2C nanocrystals are achieved and uniformly assembled on the in situ formed amorphous carbon foams. The as formed uf‐Mo2C/CF demonstrates superior hydrogen evolution activity and outstanding stability in the whole pH range. These results indicate the validity of size control and multiscale structural assembly of metal carbide nanocrystals by consideration of the overall mass transport, accessibility, and quantity, as well as the capability of the active sites toward efficient electrocatalytic hydrogen evolution reaction. This strategy can also be expanded to other energy‐related application.
author2 School of Materials Science & Engineering
author_facet School of Materials Science & Engineering
Kou, Zongkui
Wang, Tingting
Cai, Yi
Guan, Cao
Pu, Zonghua
Zhu, Changrong
Hu, Yating
Elshahawy, Abdelnaby M.
Wang, John
Mu, Shichun
format Article
author Kou, Zongkui
Wang, Tingting
Cai, Yi
Guan, Cao
Pu, Zonghua
Zhu, Changrong
Hu, Yating
Elshahawy, Abdelnaby M.
Wang, John
Mu, Shichun
author_sort Kou, Zongkui
title Ultrafine molybdenum carbide nanocrystals confined in carbon foams via a colloid-confinement route for efficient hydrogen production
title_short Ultrafine molybdenum carbide nanocrystals confined in carbon foams via a colloid-confinement route for efficient hydrogen production
title_full Ultrafine molybdenum carbide nanocrystals confined in carbon foams via a colloid-confinement route for efficient hydrogen production
title_fullStr Ultrafine molybdenum carbide nanocrystals confined in carbon foams via a colloid-confinement route for efficient hydrogen production
title_full_unstemmed Ultrafine molybdenum carbide nanocrystals confined in carbon foams via a colloid-confinement route for efficient hydrogen production
title_sort ultrafine molybdenum carbide nanocrystals confined in carbon foams via a colloid-confinement route for efficient hydrogen production
publishDate 2020
url https://hdl.handle.net/10356/138469
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