拉曼散射
基质(水族馆)
材料科学
单层
半导体
拉曼光谱
纳米技术
分子
共振(粒子物理)
光电子学
化学
光学
物理
地质学
海洋学
有机化学
粒子物理学
作者
Xiao Tang,Xingce Fan,Jun Zhou,Shuo Wang,Mingze Li,Xiangyu Hou,Kewei Jiang,Zhenhua Ni,Bei Zhao,Qi Hao,Teng Qiu
出处
期刊:Nano Letters
[American Chemical Society]
日期:2023-07-18
卷期号:23 (15): 7037-7045
被引量:26
标识
DOI:10.1021/acs.nanolett.3c01810
摘要
The chemical mechanism (CM) of surface-enhanced Raman scattering (SERS) has been recognized as a decent approach to mildly amplify Raman scattering. However, the insufficient charge transfer (CT) between the SERS substrate and molecules always results in unsatisfying Raman enhancement, exerting a substantial restriction for CM-based SERS. In principle, CT is dominated by the coupling between the energy levels of a semiconductor-molecule system and the laser wavelength, whereas precise tuning of the energy levels is intrinsically difficult. Herein, two-dimensional transition-metal dichalcogenide alloys, whose energy levels can be precisely and continuously tuned over a wide range by simply adjusting their compositions, are investigated. The alloys enable on-demand construction of the CT resonance channels to cater to the requirements of a specific target molecule in SERS. The SERS signals are highly reproducible, and a clear view of the SERS dependences on the energy levels is revealed for different CT resonance terms.
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