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  Picocavity-enhanced Raman spectroscopy of physisorbed H2 and D2 molecules

Shiotari, A., Liu, S., Trenins, G., Sugimoto, T., Wolf, M., Rossi, M., et al. (2024). Picocavity-enhanced Raman spectroscopy of physisorbed H2 and D2 molecules.

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2411.10994.pdf (Preprint), 2MB
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2411.10994.pdf
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https://arxiv.org/abs/2411.10994 (Preprint)
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 Creators:
Shiotari, A.1, Author
Liu, S.1, 2, Author
Trenins, G.3, Author           
Sugimoto, T.4, Author
Wolf, M.1, Author
Rossi, M.3, Author                 
Kumagai, T.4, Author
Affiliations:
1Department of Physical Chemistry, Fritz-Haber Institute of the Max-Planck Society, ou_persistent22              
2Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology, ou_persistent22              
3Simulations from Ab Initio Approaches, Theory Department, Max Planck Institute for the Structure and Dynamics of Matter, Max Planck Society, ou_3185035              
4nstitute for Molecular Science, National Institutes of Natural Sciences, ou_persistent22              

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Free keywords: Physics, Optics, physics.optics, Condensed Matter, Mesoscale and Nanoscale Physics, cond-mat.mes-hall
 Abstract: We report on tip-enhanced Raman scattering (TERS) of H2 and D2 molecules physisorbed within a plasmonic picocavity at a cryogenic temperature (10 K). The intense Raman peaks resulting from the rotational and vibrational transitions are observed at sub-nanometer gap distances of the junction formed by a Ag tip and Ag(111) surface. We clarify that the predominant contribution of the electromagnetic field enhancement of the picocavity to the detection of a single hydrogen molecule. The gap-distance dependent TERS reveals not only the evolution of the picocavity field, but also the interaction between the molecule and tip/surface, which exhibit nontrivial isotope effects. A significant red-shift and peak broadening of the H-H stretching as the gap distance decreases, while the D-D stretching mode is unaffected. A combination of density functional theory and reduced-dimension models reveals that a distinct anharmonicity in the mode potential of H2 is one cause of the anomalous red-shift, whereas D2 has less anharmonicity due to the geometric isotope effect.

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Language(s): eng - English
 Dates: 2024-11-17
 Publication Status: Published online
 Pages: 31
 Publishing info: -
 Table of Contents: -
 Rev. Type: No review
 Identifiers: arXiv: 2411.10994
 Degree: -

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