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Please use this identifier to cite or link to this item: http://ntour.ntou.edu.tw:8080/ir/handle/987654321/41319

Title: Photoassisted photoluminescence fine-tuning of gold nanodots through free radical-mediated ligand-assembly
Authors: Tseng, Yu-Ting;Cherng, Rochelle;Harroun, Scott G.;Yuan, Zhiqin;Lin, Tai-Yuan;Wu, Chien-Wei;Chang, Huan-Tsung;Huang, Chih-Ching
Contributors: 國立臺灣海洋大學:光電科學研究所
Date: 2016
Issue Date: 2017-02-14T05:54:04Z
Publisher: Nanoscale
Abstract: Abstract: In this study, we have developed a simple photoassisted ligand assembly to fine-tune the photoluminescence (PL) of (11-mercaptoundecyl)-N,N,N-trimethylammonium bromide-capped gold nanodots (11-MUTAB–Au NDs). The 11-MUTAB–Au NDs (size: ca. 1.8 nm), obtained from the reaction of gold nanoparticles (ca. 3 nm) and 11-MUTAB, exhibited weak, near-infrared (NIR) PL at 700 nm with a quantum yield (QY) of 0.37% upon excitation at 365 nm. The PL QY of the Au NDs increased to 11.43% after reaction with 11-mercaptoundecanoic acid (11-MUA) for 30 min under ultraviolet (UV) light, which was accompanied by a PL wavelength shift to the green region (∼520 nm). UV-light irradiation accelerates 11-MUA assembly on the 11-MUTABAu NDs (11-MUA/11-MUTAB−Au NDs) through a radical-mediated reaction. Furthermore, the PL wavelength of the 11-MUA/11-MUTAB−Au NDs can be switched to 640 nm via cysteamine under UV-light irradiation. We propose that the PL of the Au NDs with NIR and visible emissions was originally from the surface thiol–Au complexes and the Au core, respectively. These dramatically different optical properties of the Au NDs were due to variation in the surface ligands, as well as the densities and surface oxidant states of the surface Au atoms/ions. These effects can be controlled by assembling surface thiol ligands and accelerated by UV irradiation.
Relation: 8
URI: http://ntour.ntou.edu.tw:8080/ir/handle/987654321/41319
Appears in Collections:[光電科學研究所] 期刊論文

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