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单分子尖端增强拉曼光谱中的化学增强与猝灭

Chemical Enhancement and Quenching in Single-Molecule Tip-Enhanced Raman Spectroscopy.

作者信息

Yang Ben, Chen Gong, Ghafoor Atif, Zhang Yu-Fan, Zhang Xian-Biao, Li Hang, Dong Xiao-Ru, Wang Rui-Pu, Zhang Yang, Zhang Yao, Dong Zhen-Chao

机构信息

Hefei National Research Center for Physical Sciences at the Microscale and CAS Center for Excellence in Quantum Information and Quantum Physics, University of Science and Technology of China, Hefei, Anhui, 230026, China.

School of Physics and Department of Chemical Physics, University of Science and Technology of China Hefei, Anhui, 230026, China.

出版信息

Angew Chem Int Ed Engl. 2023 Mar 20;62(13):e202218799. doi: 10.1002/anie.202218799. Epub 2023 Feb 16.

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.

摘要

尽管在表面增强拉曼光谱(SERS)方面进行了深入研究,但化学效应对拉曼信号的影响机制仍然难以捉摸。在此,我们通过对具有不同但可控接触环境的单个平面锌酞菁(ZnPc)分子进行针尖增强拉曼光谱(TERS)来研究此类化学效应。发现当形成针尖 - 分子点接触时,TERS信号会显著增强。提出了一种综合物理化学机制来解释这种增强,即通过产生基态电荷转移诱导的垂直拉曼极化率,该极化率会被纳米腔中的强垂直等离子体激元场进一步增强。相比之下,发现从化学吸附在基底上的扁平ZnPc获得的TERS信号强烈猝灭,这可通过界面动态电荷转移引起的拉曼极化率筛选效应来解释。我们的结果为理解TERS/SERS增强和猝灭中的化学效应提供了深刻见解。

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