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In relation to this article, we declare that there is no conflict of interest.
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Received June 6, 2019
Accepted August 9, 2019
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Photothermal performance of plasmonic patch with gold nanoparticles embedded on polymer matrix

1Department of Chemical Engineering, Kwangwoon University, 20 Kwangwoon-ro, Nowon-gu, Seoul 01897, Korea 2Department of Chemical Engineering, Ryerson University, 350 Victoria St, Toronto, Ontario M5B 2N2, Canada 3Keenan Research Centre for Biomedical Science, St. Michael’s Hospital, Toronto, Canada
chpark@kw.ac.kr
Korean Journal of Chemical Engineering, October 2019, 36(10), 1746-1751(6), 10.1007/s11814-019-0361-4
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Abstract

Under light irradiation, gold nanoparticles (AuNPs) reveal the surface plasmon feature, i.e., the occurrence of the collective excitation of the free electrons of NPs. Plasmon relaxation, as well as excitation, induced by light absorption, could be used to increase the local temperature via conversion of light to heat. This photothermal effect can be enhanced by control of the morphology and structure of NPs in the near-infrared (NIR) region. Recently, the use of an NP-composited polymer as a heating patch with a good photothermal performance was suggested for biomedical applications. Herein, AuNPs embedded on polydimethylsiloxane (PDMS) films (Au-PDMS) were successfully prepared with an in-situ synthesis method without a reducing agent. Their photothermal performance was measured with an IR camera under 808 nm NIR irradiation, and a mechanical stretching test for the Au-PDMS films was conducted to investigate the effect of the AuNPs’ density on the photothermal performance. The surface temperature of the films, which reached 120 °C within 1min, is also adjustable with mechanical stretching (strain change). This is due to the decrease of the AuNPs density with widening interparticle distance between them.

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