Key Laboratory of Luminescent and Real-Time Analytical Chemistry (Southwest University), Ministry of Education, College of Pharmaceutical Sciences, Southwest University , Chongqing 400716, P. R. China.
College of Chemistry and Chemical Engineering, Southwest University , Chongqing 400715, P. R. China.
ACS Nano. 2017 Feb 28;11(2):2085-2093. doi: 10.1021/acsnano.6b08282. Epub 2017 Jan 31.
Understanding the photoinduced electron transfer (PET) mechanism is vital to improving the photoelectric conversion efficiency for solar energy materials and photosensitization systems. Herein, we visually demonstrate the PET process by real-time monitoring the photoinduced chemical transformation of p-aminothiophenol (p-ATP), an important SERS signal molecule, to 4,4'-dimercaptoazobenzene on single silver nanoparticles (AgNPs) with a localized surface plasmon resonance (LSPR) spectroscopy coupled dark-field microscopy. The bidirectional LSPR scattering spectral shifts bathochromically at first and hypsochromically then, which are caused by the electron transfer delay of p-ATP, disclose the PET path from p-ATP to O through AgNPs during the reaction, and enable us to digitalize the corresponding electron loss and gain on the surface of AgNP at different time periods. This visualized PET process could provide a simple and efficient approach to explore the nature of PET and help to interpret the SERS mechanism in terms of p-ATP.
了解光诱导电子转移(PET)机制对于提高太阳能材料和光敏化系统的光电转换效率至关重要。在这里,我们通过实时监测局部表面等离子体共振(LSPR)光谱与暗场显微镜联用下,p-氨基苯硫酚(p-ATP)这种重要的 SERS 信号分子向 4,4'-二巯基偶氮苯的光诱导化学转化,直观地展示了 PET 过程。p-ATP 的电子转移延迟导致 LSPR 散射光谱先红移后蓝移,揭示了反应过程中 p-ATP 通过 AgNPs 向 O 的 PET 途径,并使我们能够在不同时间段对 AgNP 表面上相应的电子损耗和增益进行数字化。这种可视化的 PET 过程为探索 PET 的本质提供了一种简单而有效的方法,并有助于根据 p-ATP 来解释 SERS 机制。