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Single-molecule tip-enhanced Raman spectroscopy of C60 on the Si(111)-(7x7) surface

MPS-Authors
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Cirera,  Borja       
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

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Liu,  Shuyi       
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

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Park,  Youngwook       
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

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Wolf,  Martin       
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

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Shiotari,  Akitoshi       
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

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Kumagai,  Takashi       
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

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Citation

Cirera, B., Liu, S., Park, Y., Ikutaro Hamada, I. H., Wolf, M., Shiotari, A., et al. (2024). Single-molecule tip-enhanced Raman spectroscopy of C60 on the Si(111)-(7x7) surface. Physical Chemistry Chemical Physics, 26(32), 21325-21331. doi:10.1039/D4CP01803F.


Cite as: https://hdl.handle.net/21.11116/0000-000F-B68E-4
Abstract
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)-(7×7) 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.