Tip-enhanced sum frequency generation spectroscopy using temporally asymmetric pulse for detecting weak vibrational signals

A Atsunori Sakurai (Institute for Molecular Science, National Institutes of Natural Sciences 1 , Okazaki 444-8585,) S Shota Takahashi T Tatsuto Mochizuki (Institute for Molecular Science, National Institutes of Natural Sciences 1 , Okazaki 444-8585,) T Tomonori Hirano (Department of Chemistry, Graduate School of Science) A Akihiro Morita (Department of Chemistry, Graduate School of Science) T Toshiki Sugimoto (Institute for Molecular Science, National Institutes of Natural Sciences 1 , Okazaki 444-8585,)

Abstract

Vibrational sum frequency generation (SFG) spectroscopy is a powerful technique for investigating molecular structures, orientations, and dynamics at surfaces. However, its spatial resolution is fundamentally restricted to the micrometer scale by the optical diffraction limit. Tip-enhanced SFG (TE-SFG) using a scanning tunneling microscope has been developed to overcome this limitation. The acquired spectra exhibit characteristic dips originating from vibrational responses located within the strong broadband non-resonant background (NRB), which distorts and obscures the molecular signals. By making the second pulse temporally asymmetric and introducing a controlled delay between the first and second laser pulses, the NRB was effectively suppressed, which led to an optimized ratio between the resonant and non-resonant signals, thereby maximizing the contrast of an interferometric signal and improving the detectability of weak vibrational signals. This interference also made it possible to determine absolute molecular orientations. Furthermore, forward- and backward-scattered signals were simultaneously detected, conclusively confirming that the observed signals originated from tip enhancement rather than far-field contributions. Finally, the signal enhancement factor in TE-SFG was estimated to be 6.3 × 106 − 1.3 × 107, based on the experimental data. This TE-SFG technique overcomes the optical diffraction limit and enables the investigation of molecular vibrations at surfaces with unprecedented detail.

Article Details

Volume / Issue Vol. 164, Issue 7
Published February 21, 2026
ISSN 0021-9606
Publisher American Institute of Physics

Journal Info

The Journal of Chemical Physics

American Institute of Physics

ISSN: 0021-9606 Physical Sciences

Authors (6)

A

Atsunori Sakurai

Institute for Molecular Science, National Institutes of Natural Sciences 1 , Okazaki 444-8585,

S

Shota Takahashi

T

Tatsuto Mochizuki

Institute for Molecular Science, National Institutes of Natural Sciences 1 , Okazaki 444-8585,

T

Tomonori Hirano

Department of Chemistry, Graduate School of Science

A

Akihiro Morita

Department of Chemistry, Graduate School of Science

T

Toshiki Sugimoto

Institute for Molecular Science, National Institutes of Natural Sciences 1 , Okazaki 444-8585,