Origin of Superlinear Power Dependence of Reaction Rates in Plasmon-Driven Photocatalysis: A Case Study of Reductive Nitrothiophenol Coupling Reactions

被引:12
|
作者
Chen, Kexun [1 ]
Wang, Hui [1 ]
机构
[1] Univ South Carolina, Dept Chem & Biochem, Columbia, SC 29208 USA
基金
美国国家科学基金会;
关键词
plasmonic photocatalysis; power dependence; photothermal transduction; hot electrons; Raman thermometry; surface-enhanced Raman scattering; ALTERNATIVE MECHANISM; ASSISTED PHOTOCATALYSIS; CHEMICAL-REACTION; CHARGE-CARRIER; HOT-CARRIER; CHEM.-SCI; WAVELENGTH; NANOSCALE; CATALYSIS; PATHWAYS;
D O I
10.1021/acs.nanolett.3c00195
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The superlinear dependence of the reaction rate on the power of the excitation light, which may arise from both thermal and nonthermal effects, has been a hallmark of plasmon-driven photocatalysis on nano-structured metal surfaces. However, it remains challenging to distinguish and quantify the thermal and nonthermal effects because even slight uncertainties in measuring the local temperatures at the active surface sites may lead to significant errors in assessing thermal and nonthermal contributions to the overall reaction rates. Here we employ surface-enhanced Raman scattering as a surface-sensitive in situ spectroscopic tool to correlate detailed kinetic features of plasmon-mediated molecular trans-formations to the local temperatures at the active sites on photocatalyst surfaces. Our spectroscopic results clearly reveal that the superlinearity in the power dependence of the reaction rate observed in a plasmon-driven model reaction, specifically the reductive coupling of para-nitrothiophenol adsorbates on Ag nanoparticle surfaces, originates essentially from photothermal heating rather than nonthermal plasmonic effects.
引用
收藏
页码:2870 / 2876
页数:7
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