拉曼光谱
化学物理
分子
猝灭(荧光)
光谱学
化学
光化学
材料科学
纳米技术
光学
荧光
有机化学
量子力学
物理
作者
Ben Yang,Chen Gong,Atif Ghafoor,Yu‐Fan Zhang,Xianbiao Zhang,Hang Li,Xiao‐Ru Dong,Rui‐Pu Wang,Yang Zhang,Yao Zhang,Zhen‐Chao Dong
标识
DOI:10.1002/anie.202218799
摘要
Abstract Despite intensive research in surface enhanced Raman spectroscopy (SERS), the influence mechanism of chemical effects on Raman signals remains elusive. Here, we investigate such chemical effects through tip‐enhanced Raman spectroscopy (TERS) of a single planar ZnPc molecule with varying but controlled contact environments. TERS signals are found dramatically enhanced upon making a tip–molecule point contact. A combined physico‐chemical mechanism is proposed to explain such an enhancement via the generation of a ground‐state charge‐transfer induced vertical Raman polarizability that is further enhanced by the strong vertical plasmonic field in the nanocavity. In contrast, TERS signals from ZnPc chemisorbed flatly on substrates are found strongly quenched, which is rationalized by the Raman polarizability screening effect induced by interfacial dynamic charge transfer. Our results provide deep insights into the understanding of the chemical effects in TERS/SERS enhancement and quenching.
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