Electrochemical Surface-Enhanced Raman Spectroscopy for Aniline Adsorbed on Silver Electrodes: A DFT Study of the Anharmonic Effects of Amino Wagging Vibrational Modes

作者：Hang Shi, Tai-Rui Wu, He‐Tian Qiao, Zi-Rui Gao, Jian‐Zhang Zhou, De‐Yin Wu, Zhong‐Qun Tian · 发表于：The Journal of Physical Chemistry C · 年份：2023 · DOI：10.1021/acs.jpcc.3c02837 · 被引用次数：8 · 研究领域：Gold and Silver Nanoparticles Synthesis and Applications、Electrochemical Analysis and Applications、Chalcogenide Semiconductor Thin Films

Aniline molecules exhibit a special amino wagging vibrational mode on the surface of the silver electrode. The corresponding Raman peak not only displays enhanced Raman signals in surface-enhanced Raman spectroscopy (SERS) experiments but also shows a shift toward higher wavenumbers. This work adopts a molecule-metal cluster model to investigate the normal Raman spectra of aniline molecules and their SERS spectra adsorbed on silver electrode surfaces by density functional theory (DFT) approaches. Based on the harmonic approximation, the influence of anharmonic effects on the normal Raman and SERS spectra of aniline is further considered. Our calculated results of the anharmonic Raman spectra of free aniline molecules show that their anharmonic effect mainly comes from the amino wagging vibrational mode. Then, the anharmonic Raman spectra of aniline binding to neutral and positively charged silver clusters were calculated and compared with the harmonic Raman spectra. It was found that the coupling effect between vibrational modes also greatly affects the Raman spectral characteristics. Finally, the excited state energy gap and pre-resonance Raman spectra of the aniline–silver cluster complexes are studied, and it is believed that there may be a charge-transfer enhancement mechanism.