Modulating the Plasmon-Mediated Decarboxylation Reaction on Silver Nanoparticles by Changing the Surface Adsorption of Molecular Cocatalysts of p-Hydroxythiophenol

被引:4
|
作者
Wang, Kaili [1 ,2 ]
Zhu, Yameng [1 ,2 ]
Yu, Liuyingzi [1 ,2 ]
Jiang, Lu [1 ,2 ]
Chen, Xinya [1 ,2 ]
Lu, Zhihao [1 ,2 ]
Gao, Kun [1 ,2 ]
Kang, Xing [1 ,2 ]
Gong, Zhongyan [1 ,2 ]
Peng, Qiming [1 ,2 ]
Lu, Gang [1 ,2 ]
机构
[1] Nanjing Tech Univ, Nanjing Tech, Key Lab Flexible Elect KLOFE, Nanjing 211816, Peoples R China
[2] Nanjing Tech Univ, Nanjing Tech, Inst Adv Mat IAM, Nanjing 211816, Peoples R China
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2024年 / 128卷 / 08期
基金
中国国家自然科学基金;
关键词
CARBOXYLIC-ACID DERIVATIVES; COUPLING REACTIONS; MONOLAYERS; FUNCTIONALIZATION; NANOSTRUCTURES; HYDROGENATION; CONVERSION; SOLAR; GOLD;
D O I
10.1021/acs.jpcc.3c07887
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The decarboxylation reaction can be accelerated with the assistance of localized surface plasmon resonance under mild conditions, benefiting from the enhanced light utilization and excitation of high-energy hot carriers. However, the reaction rate remains far below the theoretical limit since plasmon-excited hot carriers easily recombine due to their ultrashort lifetime. Herein, we effectively accelerate the decarboxylation reaction of p-mercaptobenzoic acid (PMBA) on the surface of silver nanoparticles (AgNPs) by coadsorbing p-hydroxythiophenol (PHTP) molecules as molecular cocatalysts. More importantly, the period of this coadsorption is crucial to the obtained reaction rate acceleration. Compared with short-period coadsorption, long-period coadsorption could lead to a larger acceleration in reaction rate, due to the further promoted separation of plasmon-generated hot carriers. This work provides a simple, convenient, and effective strategy to boost the decarboxylation reactions on silver surfaces. This strategy holds potential for developing a variety of highly efficient plasmon-based catalysts in the near future.
引用
收藏
页码:3361 / 3369
页数:9
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