Single-molecule tip-enhanced Raman spectroscopy of C60 on the Si(111)-(7 x 7) surface

被引:1
作者
Cirera, Borja [1 ,2 ]
Liu, Shuyi [1 ,3 ]
Park, Youngwook [1 ]
Hamada, Ikutaro [4 ]
Wolf, Martin [1 ]
Shiotari, Akitoshi [1 ]
Kumagai, Takashi [1 ,5 ]
机构
[1] Fritz Haber Inst, Max Planck Soc, Dept Phys Chem, Faradayweg 4-6, D-14195 Berlin, Germany
[2] Univ Autonoma Madrid, Inst Ciencia Mat Madrid CSIC, Campus Excelencia, C Sor Juana Ines de la Cruz 3, Madrid 28049, Spain
[3] Huazhong Univ Sci & Technol, Wuhan Natl Lab Optoelect, Wuhan, Peoples R China
[4] Osaka Univ, Grad Sch Engn, Dept Precis Engn, 2-1 Yamadaoka, Suita, Osaka 5650871, Japan
[5] Inst Mol Sci, Ctr Mesoscop Sci, Okazaki 4448585, Japan
关键词
SCATTERING;
D O I
10.1039/d4cp01803f
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Tip-enhanced Raman spectroscopy (TERS), combined with low-temperature scanning tunnelling microscopy (STM), has emerged as a highly sensitive method for chemical characterization, offering even sub-molecular resolution. However, its exceptional sensitivity is generally limited to molecules adsorbed onto plasmonic surfaces. Here we demonstrate single-molecule TERS for fullerene (C60) adsorbed on the Si(111)-(7 x 7) reconstructed surface. Distinct adsorption geometries of C60 are manifested in the TERS spectra. In addition, we reveal that formation of a molecular-point-contact (MPC) drastically enhances Raman scattering and leads to the emergence of additional vibrational peaks, including overtones and combinations. In the MPC regime, the anti-Stokes peaks are observed, revealing that vibrationally excited states are populated through optical excitation of the MPC junction, whereas showing no significant vibrational heating by current flow via inelastic electron-vibration scattering. Our results will open up the possibility of applying TERS for semiconducting surfaces and studying microscopic mechanisms of vibrational heating in metal-molecule-semiconductor nanojunctions.
引用
收藏
页码:21325 / 21331
页数:7
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