Thawed Gaussian Ehrenfest dynamics

Ehrenfest dynamics is a widely used mixed quantum-classical approach for nonadiabatic molecular dynamics, whereas thawed Gaussian wavepacket dynamics provides an efficient semiclassical description of adiabatic nuclear quantum dynamics. Here, we describe thawed Gaussian Ehrenfest dynamics (TGED), which unifies and generalizes these two methods to capture both electronic nonadiabaticity and nuclear quantum effects within a single framework. The fully variational formulation of TGED is derived by applying the time-dependent variational principle to a Hartree product of electronic and Gaussian nuclear wavepackets. Replacing the effective locally quadratic molecular potential obtained from this variational treatment by alternative effective locally quadratic potentials yields an infinite family of TGED methods, of which we present several members. We analyze the limiting cases of the general formalism and show, in particular, that it reduces to conventional Ehrenfest dynamics in the classical limit for the nuclei and to thawed Gaussian wavepacket dynamics in the absence of electronic coupling. Finally, we present explicit geometric integrators for the entire family of methods and identify the conditions under which the different approximations become exact.

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Publication Details

Journal
The Journal of Chemical Physics
Published
2026-10-06
DOI
https://doi.org/10.1063/5.0352624
Primary Topic
Spectroscopy and Quantum Chemical Studies
Type
article
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article

Thawed Gaussian Ehrenfest dynamics

Jiří J. L. Vaníček
The Journal of Chemical Physics
Spectroscopy and Quantum Chemical Studies
article

Thawed Gaussian Ehrenfest dynamics

Jiří J. L. Vaníček
article en

Abstract

Ehrenfest dynamics is a widely used mixed quantum-classical approach for nonadiabatic molecular dynamics, whereas thawed Gaussian wavepacket dynamics provides an efficient semiclassical description of adiabatic nuclear quantum dynamics. Here, we describe thawed Gaussian Ehrenfest dynamics (TGED), which unifies and generalizes these two methods to capture both electronic nonadiabaticity and nuclear quantum effects within a single framework. The fully variational formulation of TGED is derived by applying the time-dependent variational principle to a Hartree product of electronic and Gaussian nuclear wavepackets. Replacing the effective locally quadratic molecular potential obtained from this variational treatment by alternative effective locally quadratic potentials yields an infinite family of TGED methods, of which we present several members. We analyze the limiting cases of the general formalism and show, in particular, that it reduces to conventional Ehrenfest dynamics in the classical limit for the nuclei and to thawed Gaussian wavepacket dynamics in the absence of electronic coupling. Finally, we present explicit geometric integrators for the entire family of methods and identify the conditions under which the different approximations become exact.

The Journal of Chemical PhysicsVol. 165(13)
École Polytechnique Fédérale de Lausanne (CH)
Openalex Percentile: Top 45%
Spectroscopy and Quantum Chemical Studies
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