Tunable Chiral Plasmonic Activities Enabled via Stimuli Responsive Micro-Origami.

assemblies chiroptical effects micro-origami plasmonic nanoparticles responsive polymers

Journal

Advanced materials (Deerfield Beach, Fla.)
ISSN: 1521-4095
Titre abrégé: Adv Mater
Pays: Germany
ID NLM: 9885358

Informations de publication

Date de publication:
Nov 2023
Historique:
revised: 21 07 2023
received: 18 04 2023
medline: 25 7 2023
pubmed: 25 7 2023
entrez: 25 7 2023
Statut: ppublish

Résumé

Chiral plasmonic nanomaterials with distinctive circularly polarized light-dependent optical responses over a broad range of frequency have great potential for photonic and biomedical applications. However, it still remains challenging to fabricate 3D plasmonic chiral micro-constructs with readily modulated chiroptical properties over the magnitude of ellipticity, mode frequency, and switchable handedness, especially in the vis-NIR range. In this study, polymeric micro-origami-based 3D plasmonic chiral structures are constructed through self-rolling of gold  nanospheres (AuNSs)-decorated polymeric micro-sheets. Spherical AuNSs are assembled as highly ordered linear chains on 2D rectangular micro-sheets by polydimethylsiloxane-wrinkle assisted assembly. Upon rolling the micro-sheets to micro-tubules, the AuNS chains transform into 3D helices. The AuNS-assembled helices induce collective plasmonic modes propagating in a helical manner, leading to a strong chiral response over the vis-NIR range. The circular dichroism (CD) is measured to be as high as hundreds of millidegree, and the position and sign of CD peaks are actively modulated by controlling the orientated angle of AuNS chains, enabled by tuning the collective plasmonic modes. This micro-origami-based strategy incorporates the incompatible 2D assembly technique with 3D chiral structures, opening up an intriguing way toward constructing chiral plasmonic structures and modulating chiroptical effects based on responsive polymeric materials.

Identifiants

pubmed: 37489842
doi: 10.1002/adma.202303595
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2303595

Subventions

Organisme : National Natural Science Foundation of China
ID : 21975160
Organisme : National Natural Science Foundation of China
ID : 12004344
Organisme : National Natural Science Foundation of China
ID : 21961132023
Organisme : Shanghai Sailing Program
ID : 22YF1428000
Organisme : Double First-Class Initiative Fund of ShanghaiTech University
ID : SYLDX006
Organisme : German Research Foundation
ID : 451785257
Organisme : Alexander von Humboldt Foundation

Informations de copyright

© 2023 Wiley-VCH GmbH.

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Auteurs

Yisheng He (Y)

School of Physical Science and Technology, Shanghai Tech University, 393 Huaxia Middle Rd. Pudong, Shanghai, 201210, China.

Haoyu Li (H)

Department of Physics, University of Science and Technology Beijing, 30 Xueyuan Rd., Beijing, 10008, China.

Anja Maria Steiner (AM)

Institute of Physical Chemistry and Polymer Physics, Leibniz-Institut für Polymerforschung Dresden e.V., Hohe Strasse 6, 01069, Dresden, Germany.

Andreas Fery (A)

Institute of Physical Chemistry and Polymer Physics, Leibniz-Institut für Polymerforschung Dresden e.V., Hohe Strasse 6, 01069, Dresden, Germany.

Yuan Zhang (Y)

Key Laboratory of Material Physics Ministry of Education, School of Physics and Microelectronics, Zhengzhou University, 100 Kexue Ave., Zhengzhou, 450052, China.
Institute of Quantum Materials and Physics, Henan Academy of Sciences, 266 Mingli Rd., Zhengzhou, 450046, China.

Chunhong Ye (C)

School of Physical Science and Technology, Shanghai Tech University, 393 Huaxia Middle Rd. Pudong, Shanghai, 201210, China.

Classifications MeSH