Gorbunova Alina, Votkina Daria E, Semyonov Oleg, Kogolev Dmitry, Joly Jean-Patrick, Marque Sylvain R A, Mokkah Junais Habeeb, Gahlawat Soniya, Valtiner Markus, Chevalier Odile, Postnikov Pavel S, Guselnikova Olga
Research School of Chemistry and Applied Biomedical Sciences, Tomsk Polytechnic University, Tomsk 634050, Russian Federation.
Institute of Applied Physics, Vienna University of Technology, Vienna 1040, Austria.
ACS Catal. 2025 Jun 13;15(13):11163-11176. doi: 10.1021/acscatal.5c01129. eCollection 2025 Jul 4.
The progress in plasmonic chemistry requires research on energy transfer, mechanisms, and materials discovery. In this pursuit, there are >3000 papers applying the azo coupling of 4-nitrothiophenol (PNTP) as a model reaction. Here, we challenge the status of this reaction as a model due to experimental evidence of thiol desorption during plasmon excitation using laser irradiation monitored by X-ray photoelectron spectroscopy (XPS) as an analytic technique. The azo coupling was performed on commonly used Au nanoparticles (NPs) coated with PNTP and confirmed by Raman spectroscopy and XPS. Changes in the N 1s and S 2p spectral regions indicated the cleavage of the Au-S bond, accompanied by thiol oxidation. Based on XPS data, we hypothesized a chemical pathway and a kinetic model that surpasses previously used simple models in complexity, making it challenging to draw reliable conclusions. The dissociation of the Au-S bond is triggered by plasmonic heating, supported by experimentally and theoretically determined local temperatures exceeding the thiol desorption temperature. The azo coupling reaction does not fit within the requirements of the model one, which should be simple and proceed with structurally evidenced products. As one of the alternative reactions, we suggest alkoxyamine homolysis tracked by electron paramagnetic resonance spectroscopy because of known products and the simple kinetic model. Applications of suitable model reactions accelerate discoveries in plasmon catalysis.
等离子体化学的进展需要对能量转移、机制和材料发现进行研究。在这一探索过程中,有超过3000篇论文将4-硝基硫酚(PNTP)的偶氮偶联作为模型反应。在此,我们对该反应作为模型的地位提出质疑,因为使用X射线光电子能谱(XPS)作为分析技术监测激光照射下等离子体激发过程中硫醇解吸的实验证据。偶氮偶联反应在涂有PNTP的常用金纳米颗粒(NPs)上进行,并通过拉曼光谱和XPS进行了确认。N 1s和S 2p光谱区域的变化表明Au-S键的断裂,同时伴有硫醇氧化。基于XPS数据,我们假设了一个化学途径和一个动力学模型,其复杂性超过了先前使用的简单模型,这使得得出可靠结论具有挑战性。Au-S键的解离是由等离子体加热引发的,实验和理论确定的局部温度超过硫醇解吸温度为此提供了支持。偶氮偶联反应不符合模型反应的要求,模型反应应该简单且产物具有结构证据。作为替代反应之一,由于已知产物和简单的动力学模型,我们建议通过电子顺磁共振光谱跟踪烷氧基胺均裂反应。合适的模型反应的应用加速了等离子体催化领域的发现。