2016/04/25 by Alexander Humeniuk, Roland Mitrić, Humeniuk, Alexander +1
Chemistry · Physics and Astronomy · #Advanced Chemical Physics Studies #Chemical Physics (physics.chem-ph) #FOS: Physical sciences #Molecular spectroscopy and chirality #Quantum Physics (quant-ph) #Spectroscopy and Quantum Chemical Studies
paper · pdf · doi:10.48550/arxiv.1604.07185
openalex publication_date 2016/04/25 · openalex created_date 2016/07/22 · openalex updated_date 2026/07/28
Direct dynamics methods using Gaussian wavepackets have to rely only on local properties, such as gradients and hessians at the center of the wavepacket, so as to be compatible with the usual quantum chemistry methods. Matrix elements of the potential energy surfaces between wavepackets therefore usually have to be approximated. It is shown, that if a modified form of valence bond theory is used instead of the usual MO-based theories, the matrix elements can be obtained exactly. This is so because the molecular Hamiltonian only contains the Coulomb potential, for which matrix elements between different basis functions (consisting of Gaussian nuclear and electronic orbitals) are all well-known. In valence bond theory the self-consistent field calculation can be avoided so that the matrix elements are analytical functions of the nuclear coordinates. A method for simulating non-adiabatic quantum dynamics is sketched, where coherent state trajectories are propagated "on the fly" on adiabatic potential energy surfaces without making approximations to the matrix elements responsible for the coupling between trajectories.