Sum-frequency generation spectroscopy of the libration mode at the air/water interface: Electric quadrupole effects

Based on ab initio molecular dynamics simulations and quantum chemistry calculations, we compute the sum-frequency generation (SFG) spectroscopy of the interfacial water libration mode by incorporating the electric dipole, electric quadrupole, and magnetic dipole contributions. The results demonstrate that the electric quadrupole contribution dominates the spectrum, while the magnetic dipole contribution is non-negligible. In contrast, the electric dipole contribution is minimal due to the weak polarizability derivative. These findings are consistent with experimental SFG spectroscopy featuring a prominent peak at 834 cm-1, which can only be accurately reproduced when both the electric quadrupole and magnetic dipole terms are included. The dominance of the electric quadrupole effect is attributed to the delocalized electron density distribution inherent to librational motion, which extends beyond individual water molecules via hydrogen-bonding networks.

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Publication Details

Journal
The Journal of Chemical Physics
Published
2026-03-09
DOI
https://doi.org/10.1063/5.0322043
Primary Topic
Spectroscopy and Quantum Chemical Studies
Type
article
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article

Sum-frequency generation spectroscopy of the libration mode at the air/water interface: Electric quadrupole effects

Wang Wei, Ren-Hui Zheng
The Journal of Chemical Physics
Spectroscopy and Quantum Chemical Studies
article

Sum-frequency generation spectroscopy of the libration mode at the air/water interface: Electric quadrupole effects

Wang Wei, Ren-Hui Zheng
article en

Abstract

Based on ab initio molecular dynamics simulations and quantum chemistry calculations, we compute the sum-frequency generation (SFG) spectroscopy of the interfacial water libration mode by incorporating the electric dipole, electric quadrupole, and magnetic dipole contributions. The results demonstrate that the electric quadrupole contribution dominates the spectrum, while the magnetic dipole contribution is non-negligible. In contrast, the electric dipole contribution is minimal due to the weak polarizability derivative. These findings are consistent with experimental SFG spectroscopy featuring a prominent peak at 834 cm-1, which can only be accurately reproduced when both the electric quadrupole and magnetic dipole terms are included. The dominance of the electric quadrupole effect is attributed to the delocalized electron density distribution inherent to librational motion, which extends beyond individual water molecules via hydrogen-bonding networks.

The Journal of Chemical PhysicsVol. 164(10)
Anhui Medical University (CN), Chinese Academy of Sciences (CN), Beijing National Laboratory for Molecular Sciences (CN)
Clean water and sanitation
Openalex Percentile: Top 27%
Spectroscopy and Quantum Chemical Studies
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