等离子体子
热点(计算机编程)
激发态
拉曼光谱
拉曼散射
谱线
分子物理学
分子振动
星团(航天器)
斑点
材料科学
分子
化学
化学物理
光学
原子物理学
光电子学
物理
物理化学
操作系统
有机化学
计算机科学
程序设计语言
天文
作者
Hyun-Hang Shin,Gyu Jin Yeon,Han-Kyu Choi,Sang-Min Park,Kang Sup Lee,Zee Hwan Kim
出处
期刊:Nano Letters
[American Chemical Society]
日期:2017-12-05
卷期号:18 (1): 262-271
被引量:100
标识
DOI:10.1021/acs.nanolett.7b04052
摘要
The existence of sub-nanometer plasmonic hot-spots and their relevance in spectroscopy and microscopy applications remain elusive despite a few recent theoretical and experimental evidence supporting this possibility. In this Letter, we present new spectroscopic evidence suggesting that Angstrom-sized hot-spots exist on the surfaces of plasmon-excited nanostructures. Surface-enhanced Raman scattering (SERS) spectra of 4,4'-biphenyl dithiols placed in metallic junctions show simultaneously blinking Stokes and anti-Stokes spectra, some of which exhibit only one prominent vibrational peak. The activated vibrational modes were found to vary widely between junction sites. Such site-specific, single-peak spectra could be successfully modeled using single-molecule SERS induced by a hot-spot with a diameter no larger than 3.5 Å, located at the specific molecular sites. Furthermore, the model, which assumes the stochastic creation of hot-spots on locally flat metallic surfaces, consistently reproduces the intensity distributions and occurrence statistics of the blinking SERS peaks, further confirming that the sources of the hot-spots are located on the metallic surfaces. This result not only provides compelling evidence for the existence of Angstrom-sized hot-spots but also opens up the new possibilities for the vibrational and electronic control of single-molecule photochemistry and real-space visualization of molecular vibration modes.
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