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Light-tunable plasmonic nanoarchitectures using gold nanoparticle-Azobenzene-Containing cationic surfactant complexes

dc.contributor.authorLysyakova, Liudmilaen
dc.contributor.authorLomadze, Ninoen
dc.contributor.authorNeher, Dieteren
dc.contributor.authorMaximova, Kseniaen
dc.contributor.authorKabashin, Andrei V.en
dc.contributor.authorSanter, Svetlanaen
dc.date.accessioned2025-12-29T10:40:37Z
dc.date.available2025-12-29T10:40:37Z
dc.date.issued2015-02-19en
dc.description.abstractWhen arranged in a proper nanoaggregate architecture, gold nanoparticles can offer controllable plasmon-related absorption/scattering, yielding distinct color effects that depend critically on the relative orientation and distance between nanoparticle constituents. Herein, we report on the implementation of novel plasmonic nanoarchitectures based on complexes between gold nanoparticles and an azobenzene-modified cationic surfactant that can exhibit a light-tunable plasmonic response. The formation of such complexes becomes possible through the use of strongly negatively charged bare gold nanoparticles (∼10-nm diameter) prepared by the method of laser ablation in deionized water. Driven by electrostatic interactions, the cationic surfactant molecules attach and form a shell around the negatively charged nanoparticles, resulting in neutralization of the particle charge or even overcompensation beyond which the nanoparticles become positively charged. At low and high surfactant concentrations, Au nanoparticles are negatively and positively charged, respectively, and are represented by single species due to electric repulsion effects having absorption peaks around 523-527 nm, whereas at intermediate concentrations, the Au nanoparticles become neutral, forming nanoscale 100-nm clusterlike aggregates and exhibiting an additional absorption peak at λ > 600 nm and a visible change in the color of the solution from red to blue. Because of the presence of the photosensitive azobenzene unit in the surfactant tail that undergoes trans-to-cis isomerization under irradiation with UV light, we then demonstrate a light-controlled nanoclustering of nanoparticles, yielding a switch in the plasmonic absorption band and a related change in the solution color. The formed hybrid architectures with a light-controlled plasmonic response could be important for a variety of tasks, including biomedical, surface-enhanced Raman spectroscopy (SERS), data transmission, and storage applications.en
dc.description.statusPeer-revieweden
dc.format.extent9en
dc.identifier.issn1932-7447en
dc.identifier.otherORCID:/0000-0001-9531-8529/work/162952792en
dc.identifier.scopus84923381569en
dc.identifier.urihttps://hdl.handle.net/1885/733797295
dc.language.isoenen
dc.rightsPublisher Copyright: © 2015 American Chemical Society.en
dc.sourceJournal of Physical Chemistry Cen
dc.titleLight-tunable plasmonic nanoarchitectures using gold nanoparticle-Azobenzene-Containing cationic surfactant complexesen
dc.typeJournal articleen
dspace.entity.typePublicationen
local.bibliographicCitation.lastpage3770en
local.bibliographicCitation.startpage3762en
local.contributor.affiliationLysyakova, Liudmila; University of Potsdamen
local.contributor.affiliationLomadze, Nino; University of Potsdamen
local.contributor.affiliationNeher, Dieter; University of Potsdamen
local.contributor.affiliationMaximova, Ksenia; Aix-Marseille Universitéen
local.contributor.affiliationKabashin, Andrei V.; Aix-Marseille Universitéen
local.contributor.affiliationSanter, Svetlana; University of Potsdamen
local.identifier.citationvolume119en
local.identifier.doi10.1021/jp511232gen
local.identifier.pureb486c3de-3d7b-4fd8-ac26-3238889c0992en
local.identifier.urlhttps://www.scopus.com/pages/publications/84923381569en
local.type.statusPublisheden

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