Synthesis of substrate-bound Au nanowires via an active surface growth mechanism

Advancing synthetic capabilities is important for the development of nanoscience and nanotechnology. The synthesis of nanowires has always been a challenge, as it requires asymmetric growth of symmetric crystals. Here, we report a distinctive synthesis of substrate-bound Au nanowires. This template-...

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Main Authors: Wang, Xinglong, Wu, Xuesong, He, Jiating, Tao, Xiaolin, Li, Hongyan, Zhao, Gui, Wang, Yawen, Chen, Hongyu
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2018
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Online Access:https://hdl.handle.net/10356/89758
http://hdl.handle.net/10220/46508
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-897582023-02-28T19:33:19Z Synthesis of substrate-bound Au nanowires via an active surface growth mechanism Wang, Xinglong Wu, Xuesong He, Jiating Tao, Xiaolin Li, Hongyan Zhao, Gui Wang, Yawen Chen, Hongyu School of Physical and Mathematical Sciences Metal Nanowire DRNTU::Science::Chemistry Gold Advancing synthetic capabilities is important for the development of nanoscience and nanotechnology. The synthesis of nanowires has always been a challenge, as it requires asymmetric growth of symmetric crystals. Here, we report a distinctive synthesis of substrate-bound Au nanowires. This template-free synthesis employs thiolated ligands and substrate adsorption to achieve the continuous asymmetric deposition of Au in solution at ambient conditions. The thiolated ligand prevented the Au deposition on the exposed surface of the seeds, so the Au deposition only occurs at the interface between the Au seeds and the substrate. The side of the newly deposited Au nanowires is immediately covered with the thiolated ligand, while the bottom facing the substrate remains ligand-free and active for the next round of Au deposition. We further demonstrate that this Au nanowire growth can be induced on various substrates, and different thiolated ligands can be used to regulate the surface chemistry of the nanowires. The diameter of the nanowires can also be controlled with mixed ligands, in which another "bad" ligand could turn on the lateral growth. With the understanding of the mechanism, Au nanowire-based nanostructures can be designed and synthesized. Published version 2018-11-01T03:58:05Z 2019-12-06T17:32:48Z 2018-11-01T03:58:05Z 2019-12-06T17:32:48Z 2018 Journal Article Wang, X., Wu, X., He, J., Tao, X., Li, H., Zhao, G., . . . Chen, H. (2018). Synthesis of substrate-bound Au nanowires via an active surface growth mechanism. Journal of Visualized Experiments, 137, e57808-. doi:10.3791/57808 https://hdl.handle.net/10356/89758 http://hdl.handle.net/10220/46508 10.3791/57808 en Journal of Visualized Experiments © 2018 Journal of Visualized Experiments. This paper was published in Journal of Visualized Experiments and is made available as an electronic reprint (preprint) with permission of Journal of Visualized Experiments. The published version is available at: [http://dx.doi.org/10.3791/57808]. One print or electronic copy may be made for personal use only. Systematic or multiple reproduction, distribution to multiple locations via electronic or other means, duplication of any material in this paper for a fee or for commercial purposes, or modification of the content of the paper is prohibited and is subject to penalties under law. 7 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 Nanowire
DRNTU::Science::Chemistry
Gold
spellingShingle Metal Nanowire
DRNTU::Science::Chemistry
Gold
Wang, Xinglong
Wu, Xuesong
He, Jiating
Tao, Xiaolin
Li, Hongyan
Zhao, Gui
Wang, Yawen
Chen, Hongyu
Synthesis of substrate-bound Au nanowires via an active surface growth mechanism
description Advancing synthetic capabilities is important for the development of nanoscience and nanotechnology. The synthesis of nanowires has always been a challenge, as it requires asymmetric growth of symmetric crystals. Here, we report a distinctive synthesis of substrate-bound Au nanowires. This template-free synthesis employs thiolated ligands and substrate adsorption to achieve the continuous asymmetric deposition of Au in solution at ambient conditions. The thiolated ligand prevented the Au deposition on the exposed surface of the seeds, so the Au deposition only occurs at the interface between the Au seeds and the substrate. The side of the newly deposited Au nanowires is immediately covered with the thiolated ligand, while the bottom facing the substrate remains ligand-free and active for the next round of Au deposition. We further demonstrate that this Au nanowire growth can be induced on various substrates, and different thiolated ligands can be used to regulate the surface chemistry of the nanowires. The diameter of the nanowires can also be controlled with mixed ligands, in which another "bad" ligand could turn on the lateral growth. With the understanding of the mechanism, Au nanowire-based nanostructures can be designed and synthesized.
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Wang, Xinglong
Wu, Xuesong
He, Jiating
Tao, Xiaolin
Li, Hongyan
Zhao, Gui
Wang, Yawen
Chen, Hongyu
format Article
author Wang, Xinglong
Wu, Xuesong
He, Jiating
Tao, Xiaolin
Li, Hongyan
Zhao, Gui
Wang, Yawen
Chen, Hongyu
author_sort Wang, Xinglong
title Synthesis of substrate-bound Au nanowires via an active surface growth mechanism
title_short Synthesis of substrate-bound Au nanowires via an active surface growth mechanism
title_full Synthesis of substrate-bound Au nanowires via an active surface growth mechanism
title_fullStr Synthesis of substrate-bound Au nanowires via an active surface growth mechanism
title_full_unstemmed Synthesis of substrate-bound Au nanowires via an active surface growth mechanism
title_sort synthesis of substrate-bound au nanowires via an active surface growth mechanism
publishDate 2018
url https://hdl.handle.net/10356/89758
http://hdl.handle.net/10220/46508
_version_ 1759854666119643136