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Dual Plasmon Resonances and Tunable Electric Field in Structure-Adjustable Au Nanoflowers for Improved SERS and Photocatalysis

Flower-like metallic nanocrystals have shown great potential in the fields of nanophononics and energy conversion owing to their unique optical properties and particular structures. Herein, colloid Au nanoflowers with different numbers of petals were prepared by a steerable template process. The str...

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Autores principales: Zhao, Yi-Xin, Kang, Hao-Sen, Zhao, Wen-Qin, Chen, You-Long, Ma, Liang, Ding, Si-Jing, Chen, Xiang-Bai, Wang, Qu-Quan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8466837/
https://www.ncbi.nlm.nih.gov/pubmed/34578492
http://dx.doi.org/10.3390/nano11092176
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author Zhao, Yi-Xin
Kang, Hao-Sen
Zhao, Wen-Qin
Chen, You-Long
Ma, Liang
Ding, Si-Jing
Chen, Xiang-Bai
Wang, Qu-Quan
author_facet Zhao, Yi-Xin
Kang, Hao-Sen
Zhao, Wen-Qin
Chen, You-Long
Ma, Liang
Ding, Si-Jing
Chen, Xiang-Bai
Wang, Qu-Quan
author_sort Zhao, Yi-Xin
collection PubMed
description Flower-like metallic nanocrystals have shown great potential in the fields of nanophononics and energy conversion owing to their unique optical properties and particular structures. Herein, colloid Au nanoflowers with different numbers of petals were prepared by a steerable template process. The structure-adjustable Au nanoflowers possessed double plasmon resonances, tunable electric fields, and greatly enhanced SERS and photocatalytic activity. In the extinction spectra, Au nanoflowers had a strong electric dipole resonance located around 530 to 550 nm. Meanwhile, a longitudinal plasmon resonance (730~760 nm) was obtained when the number of petals of Au nanoflowers increased to two or more. Numerical simulations verified that the strong electric fields of Au nanoflowers were located at the interface between the Au nanosphere and Au nanopetals, caused by the strong plasmon coupling. They could be further tuned by adding more Au nanopetals. Meanwhile, much stronger electric fields of Au nanoflowers with two or more petals were identified under longitudinal plasmon excitation. With these characteristics, Au nanoflowers showed excellent SERS and photocatalytic performances, which were highly dependent on the number of petals. Four-petal Au nanoflowers possessed the highest SERS activity on detecting Rhodamine B (excited both at 532 and 785 nm) and the strongest photocatalytic activity toward photodegrading methylene blue under visible light irradiation, caused by the strong multi-interfacial plasmon coupling and longitudinal plasmon resonance.
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spelling pubmed-84668372021-09-27 Dual Plasmon Resonances and Tunable Electric Field in Structure-Adjustable Au Nanoflowers for Improved SERS and Photocatalysis Zhao, Yi-Xin Kang, Hao-Sen Zhao, Wen-Qin Chen, You-Long Ma, Liang Ding, Si-Jing Chen, Xiang-Bai Wang, Qu-Quan Nanomaterials (Basel) Article Flower-like metallic nanocrystals have shown great potential in the fields of nanophononics and energy conversion owing to their unique optical properties and particular structures. Herein, colloid Au nanoflowers with different numbers of petals were prepared by a steerable template process. The structure-adjustable Au nanoflowers possessed double plasmon resonances, tunable electric fields, and greatly enhanced SERS and photocatalytic activity. In the extinction spectra, Au nanoflowers had a strong electric dipole resonance located around 530 to 550 nm. Meanwhile, a longitudinal plasmon resonance (730~760 nm) was obtained when the number of petals of Au nanoflowers increased to two or more. Numerical simulations verified that the strong electric fields of Au nanoflowers were located at the interface between the Au nanosphere and Au nanopetals, caused by the strong plasmon coupling. They could be further tuned by adding more Au nanopetals. Meanwhile, much stronger electric fields of Au nanoflowers with two or more petals were identified under longitudinal plasmon excitation. With these characteristics, Au nanoflowers showed excellent SERS and photocatalytic performances, which were highly dependent on the number of petals. Four-petal Au nanoflowers possessed the highest SERS activity on detecting Rhodamine B (excited both at 532 and 785 nm) and the strongest photocatalytic activity toward photodegrading methylene blue under visible light irradiation, caused by the strong multi-interfacial plasmon coupling and longitudinal plasmon resonance. MDPI 2021-08-25 /pmc/articles/PMC8466837/ /pubmed/34578492 http://dx.doi.org/10.3390/nano11092176 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zhao, Yi-Xin
Kang, Hao-Sen
Zhao, Wen-Qin
Chen, You-Long
Ma, Liang
Ding, Si-Jing
Chen, Xiang-Bai
Wang, Qu-Quan
Dual Plasmon Resonances and Tunable Electric Field in Structure-Adjustable Au Nanoflowers for Improved SERS and Photocatalysis
title Dual Plasmon Resonances and Tunable Electric Field in Structure-Adjustable Au Nanoflowers for Improved SERS and Photocatalysis
title_full Dual Plasmon Resonances and Tunable Electric Field in Structure-Adjustable Au Nanoflowers for Improved SERS and Photocatalysis
title_fullStr Dual Plasmon Resonances and Tunable Electric Field in Structure-Adjustable Au Nanoflowers for Improved SERS and Photocatalysis
title_full_unstemmed Dual Plasmon Resonances and Tunable Electric Field in Structure-Adjustable Au Nanoflowers for Improved SERS and Photocatalysis
title_short Dual Plasmon Resonances and Tunable Electric Field in Structure-Adjustable Au Nanoflowers for Improved SERS and Photocatalysis
title_sort dual plasmon resonances and tunable electric field in structure-adjustable au nanoflowers for improved sers and photocatalysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8466837/
https://www.ncbi.nlm.nih.gov/pubmed/34578492
http://dx.doi.org/10.3390/nano11092176
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