Third-harmonic scattering optical activity: QED theory, symmetry considerations, and quantum chemistry applications in the framework of response theory

被引:6
|
作者
Bonvicini, Andrea [1 ]
Champagne, Benoit [1 ]
机构
[1] Univ Namur, Namur Inst Struct Matter, Unit Theoret & Struct Phys Chem, Theoret Chem Lab, B-5000 Namur, Belgium
来源
JOURNAL OF CHEMICAL PHYSICS | 2023年 / 159卷 / 11期
关键词
CIRCULAR-DICHROISM; RAMAN-SCATTERING; AB-INITIO; ELECTRODYNAMICS; POLARIZATION; RAYLEIGH; TENSORS; LIGHT; SETS;
D O I
10.1063/5.0165425
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this work, expressions for the third-harmonic scattering optical activity (THS-OA) spectroscopic responses are derived by combining molecular quantum electrodynamics (QED) and response theory, allowing their computational implementation. The QED theory of THS-OA presented here is meant to be an extension of a previous study by Andrews [Symmetry 12, 1466 (2020)]. In particular, the THS-OA phenomena are described within the Power-Zienau-Woolley multipolar Hamiltonian by including the electric-dipole, magnetic-dipole, and electric-quadrupole interactions for the absorption as well as the emission processes between the dynamic electromagnetic field (the photons) and matter. Moreover, we derive the expressions for the differential scattering ratios as a function of the scattering angle defined by the wavevectors of the incident and scattered photons. We show how the pure and mixed second hyperpolarizabilities can be obtained in the framework of response theory as specific cases of a generic cubic response function, thus enabling the computational implementation of THS-OA spectroscopy. We prove the origin-independence of the theory for exact wavefunctions. Preliminary computations on a prototype chiral molecule (methyloxirane) are considered together with an analysis of the basis set convergence and of the origin-dependence.
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页数:16
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