A general soft-enveloping strategy in the templating synthesis of mesoporous metal nanostructures

Metal species have a relatively high mobility inside mesoporous silica; thus, it is difficult to introduce the metal precursors into silica mesopores and suppress the migration of metal species during a reduction process. Therefore, until now, the controlled growth of metal nanocrystals in a confine...

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Main Authors: Fang, Jixiang, Zhang, Lingling, Li, Jiang, Lu, Lu, Ma, Chuansheng, Cheng, Shaodong, Li, Zhiyuan, Xiong, Qihua, You, Hongjun
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2018
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Online Access:https://hdl.handle.net/10356/86477
http://hdl.handle.net/10220/45225
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-864772023-02-28T19:33:37Z A general soft-enveloping strategy in the templating synthesis of mesoporous metal nanostructures Fang, Jixiang Zhang, Lingling Li, Jiang Lu, Lu Ma, Chuansheng Cheng, Shaodong Li, Zhiyuan Xiong, Qihua You, Hongjun School of Physical and Mathematical Sciences Metal Mesoporous Metal species have a relatively high mobility inside mesoporous silica; thus, it is difficult to introduce the metal precursors into silica mesopores and suppress the migration of metal species during a reduction process. Therefore, until now, the controlled growth of metal nanocrystals in a confined space, i.e., mesoporous channels, has been very challenging. Here, by using a soft-enveloping reaction at the interfaces of the solid, liquid, and solution phases, we successfully control the growth of metallic nanocrystals inside a mesoporous silica template. Diverse monodispersed nanostructures with well-defined sizes and shapes, including Ag nanowires, 3D mesoporous Au, AuAg alloys, Pt networks, and Au nanoparticle superlattices are successfully obtained. The 3D mesoporous AuAg networks exhibit enhanced catalytic activities in an electrochemical methanol oxidation reaction. The current soft-enveloping synthetic strategy offers a robust approach to synthesize diverse mesoporous metal nanostructures that can be utilized in catalysis, optics, and biomedicine applications. Published version 2018-07-25T05:54:09Z 2019-12-06T16:22:55Z 2018-07-25T05:54:09Z 2019-12-06T16:22:55Z 2018 Journal Article Fang, J., Zhang, L., Li, J., Lu, L., Ma, C., Cheng, S., et al. (2018). A general soft-enveloping strategy in the templating synthesis of mesoporous metal nanostructures. Nature Communications, 9(1), 521-. https://hdl.handle.net/10356/86477 http://hdl.handle.net/10220/45225 10.1038/s41467-018-02930-9 en Nature Communications © 2018 The Author(s). This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/ licenses/by/4.0/. 9 p. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Metal
Mesoporous
spellingShingle Metal
Mesoporous
Fang, Jixiang
Zhang, Lingling
Li, Jiang
Lu, Lu
Ma, Chuansheng
Cheng, Shaodong
Li, Zhiyuan
Xiong, Qihua
You, Hongjun
A general soft-enveloping strategy in the templating synthesis of mesoporous metal nanostructures
description Metal species have a relatively high mobility inside mesoporous silica; thus, it is difficult to introduce the metal precursors into silica mesopores and suppress the migration of metal species during a reduction process. Therefore, until now, the controlled growth of metal nanocrystals in a confined space, i.e., mesoporous channels, has been very challenging. Here, by using a soft-enveloping reaction at the interfaces of the solid, liquid, and solution phases, we successfully control the growth of metallic nanocrystals inside a mesoporous silica template. Diverse monodispersed nanostructures with well-defined sizes and shapes, including Ag nanowires, 3D mesoporous Au, AuAg alloys, Pt networks, and Au nanoparticle superlattices are successfully obtained. The 3D mesoporous AuAg networks exhibit enhanced catalytic activities in an electrochemical methanol oxidation reaction. The current soft-enveloping synthetic strategy offers a robust approach to synthesize diverse mesoporous metal nanostructures that can be utilized in catalysis, optics, and biomedicine applications.
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Fang, Jixiang
Zhang, Lingling
Li, Jiang
Lu, Lu
Ma, Chuansheng
Cheng, Shaodong
Li, Zhiyuan
Xiong, Qihua
You, Hongjun
format Article
author Fang, Jixiang
Zhang, Lingling
Li, Jiang
Lu, Lu
Ma, Chuansheng
Cheng, Shaodong
Li, Zhiyuan
Xiong, Qihua
You, Hongjun
author_sort Fang, Jixiang
title A general soft-enveloping strategy in the templating synthesis of mesoporous metal nanostructures
title_short A general soft-enveloping strategy in the templating synthesis of mesoporous metal nanostructures
title_full A general soft-enveloping strategy in the templating synthesis of mesoporous metal nanostructures
title_fullStr A general soft-enveloping strategy in the templating synthesis of mesoporous metal nanostructures
title_full_unstemmed A general soft-enveloping strategy in the templating synthesis of mesoporous metal nanostructures
title_sort general soft-enveloping strategy in the templating synthesis of mesoporous metal nanostructures
publishDate 2018
url https://hdl.handle.net/10356/86477
http://hdl.handle.net/10220/45225
_version_ 1759853096538734592