Frequency-Domain Proof of the Existence of Atomic-Scale SERS Hot-Spots

被引:97
作者
Shin, Hyun-Hang [1 ]
Yeon, Gyu Jin [1 ]
Choi, Han-Kyu [1 ]
Park, Sang -Min [1 ]
Lee, Kang Sup [1 ]
Kim, Zee Hwan [1 ]
机构
[1] Seoul Natl Univ, Dept Chem, Seoul 08826, South Korea
关键词
Surface-enhanced Raman scattering; plasmonics; vibrational spectroscopy; ENHANCED RAMAN-SCATTERING; SINGLE-MOLECULE; SURFACE; SPECTROSCOPY; PLASMONS; FIELD; RESOLUTION; NANOOPTICS;
D O I
10.1021/acs.nanolett.7b04052
中图分类号
O6 [化学];
学科分类号
0703 ;
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 angstrom, 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.
引用
收藏
页码:262 / 271
页数:10
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