拉曼光谱
材料科学
分子
表面增强拉曼光谱
光谱学
纳米技术
曲面(拓扑)
化学物理
拉曼散射
化学
光学
物理
有机化学
几何学
数学
量子力学
作者
Makayla Maxine Schmidt,Alexandre G. Brolo,Nathan C. Lindquist
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-09-11
被引量:2
标识
DOI:10.1021/acsnano.4c09483
摘要
Single-molecule surface-enhanced Raman spectroscopy (SM-SERS) is a powerful experimental technique for label-free sensing, imaging, and chemical analysis. Although Raman spectroscopy itself is an extremely "feeble" phenomenon, the intense interaction of optical fields with metallic nanostructures in the form of plasmonic hotspots can generate Raman signals from single molecules. While what constitutes a true single-molecule signal has taken some years for the scientific community to establish, many SERS experiments, even those not specifically attempting single-molecule sensitivity, have observed fluctuation in both the SERS intensity and spectral features. In this Perspective, we discuss the impact that fluctuating SERS signals have had on the continuing advancement of SM-SERS, along with challenges and current and potential future applications.
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