Revealing the mechanisms of p-aminothiophenol and p-nitrothiophenol dimerizing to p,p'-dimercaptoazobenzene on plasmonic metal surfaces by tip-/surface-enhanced Raman spectroscopy

Plasmonics V Pub Date : 2020-10-10 DOI:10.1117/12.2575408
Hong Wei
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Abstract

Surface plasmon-mediated photocatalysis has attracted great interest. One model system is that p-aminothiophenol (PATP) could be dimerized into a new molecule of p,p′-dimercaptoazobenzene on noble metal surfaces under laser illumination. The mechanism of this catalytic reaction has caused wide discussion, but it is not fully understood yet. We performed a series of experiments for PATP and p-nitrothiophenol by tip-enhanced Raman spectroscopy and surface-enhanced Raman spectroscopy in a well-controlled gas environment (high vacuum, air, N2, and O2), and on different substrates (Au, Ag, Cu, Al, and corresponding oxides). The experimental results indicate that the electron acceptor or donor plays a decisive role in whether the reactions can occur or not.
利用尖端/表面增强拉曼光谱揭示对氨基噻吩和对硝基噻吩在等离子体金属表面二聚化成p,p′-二巯基偶氮苯的机理
表面等离子体介导的光催化引起了人们极大的兴趣。一个模型系统是在激光照射下,对氨基噻吩(PATP)在贵金属表面上可以二聚成一个新的p,p ' -二巯基偶氮苯分子。这种催化反应的机理引起了广泛的讨论,但尚未完全了解。我们在控制良好的气体环境(高真空、空气、N2和O2)和不同的底物(Au、Ag、Cu、Al和相应的氧化物)上,通过尖端增强拉曼光谱和表面增强拉曼光谱对PATP和对亚硝基苯酚进行了一系列实验。实验结果表明,电子受体或电子给体对反应能否发生起决定性作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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