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Aggregation of Gold Nanoparticles for Controlling Emission Polarization : Implications for Applications in Photonics

Zhou, Wenjin ; Shi, Juanzi LU ; Chen, Ruiyun LU ; Zhang, Guofeng ; Qin, Chengbing ; Hu, Jianyong ; Scheblykin, Ivan G. LU orcid and Xiao, Liantuan (2024) In ACS Applied Nano Materials 7(13). p.15025-15034
Abstract

Manipulating the light polarization properties of gold nanoparticle aggregates can facilitate their applications in sensing and imaging. However, control of the intrinsic light polarization on demand at the nanoscale is hindered by the lack of a fundamental understanding of the structure-dependent plasmon coupling in the aggregates. Here, the polarization properties of intrinsic photoluminescence (PL) and scattering of gold nanoparticle dimers and trimers are studied experimentally and computationally at the single-aggregate level. We find that the PL excitation and emission polarization degrees of the aggregates are highly correlated to the shift of their PL and scattering spectra. The results suggest that the degree of PL polarization... (More)

Manipulating the light polarization properties of gold nanoparticle aggregates can facilitate their applications in sensing and imaging. However, control of the intrinsic light polarization on demand at the nanoscale is hindered by the lack of a fundamental understanding of the structure-dependent plasmon coupling in the aggregates. Here, the polarization properties of intrinsic photoluminescence (PL) and scattering of gold nanoparticle dimers and trimers are studied experimentally and computationally at the single-aggregate level. We find that the PL excitation and emission polarization degrees of the aggregates are highly correlated to the shift of their PL and scattering spectra. The results suggest that the degree of PL polarization is dominated by the strength of the longitudinal plasmon resonance mode arising from the plasmon coupling between the two closest particles in the aggregate. While the PL direction is always along the two most strongly interacting particles in the trimers, changing the arrangement can modify the PL polarization degree. This work provides further insights into the mechanism of the plasmon coupling-induced polarized optical response of aggregated metal nanoparticles and suggests routes to achieve on-demand control of the PL light polarization. This paves the way to using the polarized optical response of plasmonic nanostructures for applications in photonics including sensing and imaging.

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author
; ; ; ; ; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
gold nanoparticle aggregates, photoluminescence, plasmon coupling, polarization, scattering, self-assembly
in
ACS Applied Nano Materials
volume
7
issue
13
pages
10 pages
publisher
The American Chemical Society (ACS)
external identifiers
  • scopus:85197601537
ISSN
2574-0970
DOI
10.1021/acsanm.4c01558
language
English
LU publication?
yes
id
b79a7da6-afe8-4884-a2d7-cfcb07f78073
date added to LUP
2024-09-23 15:29:52
date last changed
2024-09-23 15:29:52
@article{b79a7da6-afe8-4884-a2d7-cfcb07f78073,
  abstract     = {{<p>Manipulating the light polarization properties of gold nanoparticle aggregates can facilitate their applications in sensing and imaging. However, control of the intrinsic light polarization on demand at the nanoscale is hindered by the lack of a fundamental understanding of the structure-dependent plasmon coupling in the aggregates. Here, the polarization properties of intrinsic photoluminescence (PL) and scattering of gold nanoparticle dimers and trimers are studied experimentally and computationally at the single-aggregate level. We find that the PL excitation and emission polarization degrees of the aggregates are highly correlated to the shift of their PL and scattering spectra. The results suggest that the degree of PL polarization is dominated by the strength of the longitudinal plasmon resonance mode arising from the plasmon coupling between the two closest particles in the aggregate. While the PL direction is always along the two most strongly interacting particles in the trimers, changing the arrangement can modify the PL polarization degree. This work provides further insights into the mechanism of the plasmon coupling-induced polarized optical response of aggregated metal nanoparticles and suggests routes to achieve on-demand control of the PL light polarization. This paves the way to using the polarized optical response of plasmonic nanostructures for applications in photonics including sensing and imaging.</p>}},
  author       = {{Zhou, Wenjin and Shi, Juanzi and Chen, Ruiyun and Zhang, Guofeng and Qin, Chengbing and Hu, Jianyong and Scheblykin, Ivan G. and Xiao, Liantuan}},
  issn         = {{2574-0970}},
  keywords     = {{gold nanoparticle aggregates; photoluminescence; plasmon coupling; polarization; scattering; self-assembly}},
  language     = {{eng}},
  number       = {{13}},
  pages        = {{15025--15034}},
  publisher    = {{The American Chemical Society (ACS)}},
  series       = {{ACS Applied Nano Materials}},
  title        = {{Aggregation of Gold Nanoparticles for Controlling Emission Polarization : Implications for Applications in Photonics}},
  url          = {{http://dx.doi.org/10.1021/acsanm.4c01558}},
  doi          = {{10.1021/acsanm.4c01558}},
  volume       = {{7}},
  year         = {{2024}},
}