4.6 Article

Energetic Origins of Force Constants: Adding a New Dimension to the Hessian Matrix via Interacting Quantum Atoms

期刊

JOURNAL OF PHYSICAL CHEMISTRY A
卷 126, 期 48, 页码 8945-8954

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpca.2c05798

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  1. Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [2017/22741-3, 2018/08861-9]
  2. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq) [302574/2019-0]

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This paper presents a method for the decomposition of force constants in molecules, revealing their energetic origins through the decomposition of the Hessian matrix. The method is validated for a set of 30 molecules and more than 200 force constants, showing promising results.
The Interacting Quantum Atoms (IQA) energy decomposition scheme divides the total energy of a molecule into intra-and interatomic contributions. While the former relates to the kinetic and potential energies of electrons inside a unique individual atomic basin, the latter contains the Coulomb and exchange-correlation potentials between electrons from two atomic basins. Considering that the molecular energy is a sum of IQA contributions, the Hessian matrix can also be written as a sum of IQA Hessian matrices, whose elements are second derivatives of IQA terms. Herein, we present a mathematical formalism for the IQA decomposition of force constants revealing their energetic origins. The method consists of adding a new dimension to the Hessian matrix, which becomes 3N x 3N x N2, with N being the number of atoms in the molecule and N2 the number of IQA terms. Since there is no analytical method that produces the IQA second derivatives, the three-dimensional IQA Hessian is numerically calculated. When studying molecular vibrations, force constants, providing information about the nature of chemical bond and related to infrared frequencies, can be obtained by Wilson's FG method, which involves detailed manipulations of the Hessian matrix. In this paper, the methodology is reported and validated for a set of 30 molecules and more than 200 force constants and their interactions. Energetic origins of force constants are presented for diatomics and small molecules containing carbon-carbon, oxygen-oxygen, and carbon-oxygen bonds with different bond orders. It is found that bond stability and stiffness can have strikingly different energetic origins.

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