等离子体子
表面等离子共振
材料科学
分子
光化学
表面增强拉曼光谱
拉曼光谱
纳米颗粒
纳米技术
拉曼散射
化学
光电子学
有机化学
光学
物理
作者
Zhuoyao Li,Chengyu Zhang,Huixiang Sheng,Jin Wang,Yameng Zhu,Liuyingzi Yu,Junjie Wang,Qiming Peng,Gang Lü
标识
DOI:10.1021/acsami.2c08327
摘要
Localized surface plasmon resonance (LSPR) has been demonstrated to be highly effective in the initialization or acceleration of chemical reactions because of its unique optical properties. However, because of the ultrashort lifetime (fs to ps) of plasmon-generated hot carriers, the potential of LSPR in photochemical reactions has not been fully exploited. Herein, we demonstrate an acceleration of the plasmon-mediated reduction of p-nitrothiophenol (PNTP) molecules on the surface of silver nanoparticles (AgNPs) with in situ Raman spectroscopy. p-Mercaptophenylboronic acid (PMPBA) molecules coadsorbed on AgNP surfaces act as a molecular cocatalyst in the plasmon-mediated reaction, resulting in a boosting of the PNTP reduction. This boosting is attributed to the improved transfer and separation of the plasmon-generated hot carriers at the interface of the AgNPs and coadsorbed PMPBA molecules. Our finding provides a highly simple, cost-effective, and highly effective strategy to promote plasmonic photochemistry by introducing a molecular cocatalyst, and this strategy can be extended to promote various plasmon-mediated reactions.
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