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Surface‐enhanced Raman scattering of M 2 –pyrazine– M 2 (M = Cu, Ag, Au): Analysis by natural perturbation orbitals and density functional theory functional dependence
Author(s) -
Miyamoto Masaya,
Hada Masahiko
Publication year - 2020
Publication title -
journal of computational chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.907
H-Index - 188
eISSN - 1096-987X
pISSN - 0192-8651
DOI - 10.1002/jcc.26205
Subject(s) - atomic orbital , density functional theory , raman scattering , pyrazine , chemistry , perturbation theory (quantum mechanics) , molecular orbital , molecule , raman spectroscopy , molecular physics , intensity (physics) , scattering , computational chemistry , atomic physics , physics , quantum mechanics , stereochemistry , organic chemistry , electron
Here, we propose a new method to analyze various electronic properties of molecules based on natural perturbation orbitals (NPOs). We applied the proposed method to chemical enhancement of the surface‐enhanced Raman scattering (SERS) intensity of M 2 –pyrazine–M 2 (M = Cu, Ag, Au) complexes. The SERS intensity can be effectively decomposed into the contributions of four NPO pairs (1 σ– 1 σ *, 2 σ– 2 σ *, 1 π– 1 π *, and 2 π –2 π *), so NPO analysis makes the SERS intensity much easier to understand than by conventional canonical molecular orbitals. Moreover, we analyzed the dependence of the density functional theory functional on the SERS intensity. For the Ag 2 –pyrazine–Ag 2 complex, the BP86 functional overestimates the Raman intensity by about 23 times compared with coupled‐cluster singles and doubles level of theory, while the CAM‐B3LYP functional gives moderately accurate values. This overestimation arises from the inaccuracy of the energy derivative along the normal vibrational mode.