首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Plasmon-Enhanced Chemical Reaction at the Hot Spots of End-to-End Assembled Gold Nanorods
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Plasmon-Enhanced Chemical Reaction at the Hot Spots of End-to-End Assembled Gold Nanorods

机译:在端到端组装金纳米棒的热点处的等离子体增强的化学反应

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Herein, we report a centrifugal force-driven end-to-end assembly of gold nanorods (Au NRs) via the H-bonded interaction of para-aminothiophenol (p-ATP) selectively bound to the longitudinal ends of the Au NRs. The plasmonic hot spots generated due to the Au NR assembly served as a catalytic center for carrying out the photochemical coupling reaction of p-ATP to dimercaptoazobenzene (DMAB). We also demonstrate the degradation of DMAB in the presence of hydrogen peroxide (H2O2) at the plasmonic hot spot. The coupling reaction was carried out at the hot spot of the assembled Au NRs upon surface plasmon excitation using a 632.8 nm laser. Surface-enhanced Raman scattering (SERS) kinetic data indicated that the plasmon-mediated coupling reaction was 1.6-fold faster at the plasmonic hot spot of the assembled Au NRs than that on the surface of the longitudinal end of the Au NRs. This, therefore, showed a new way of carrying out photocatalytic reactions at the plasmonic hot spot with a higher reaction rate.
机译:在此,我们通过选择性地结合Au NRS的纵向端,通过对氨基噻吩醇(P-ATP)的H键合相互作用来报告金纳米棒(AU NRS)的离心力驱动的端到端组装。由于AU NR组件而产生的等离子体热点用作催化中心,用于执行P-ATP至二巯基氮苯并苯并苯苯(DMAB)的光化学偶联反应。我们还证明了在等离子体热点的过氧化氢(H2O2)存在下DMAB的降解。在使用632.8nm激光的表面等离子体激发时,在组装的Au nrs的热点进行偶联反应。表面增强的拉曼散射(SERS)动力学数据表明,在组装的Au nrs的子末端热点在组装的Au nrs的旋转热点上的速度比在Au nrs的纵向末端的表面上更快的旋转偶联反应。因此,这显示出具有更高反应速率的等离子体热点处的光催化反应的新方法。

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