Interpretation of Coupled-Cluster Many-Electron Dynamics in Terms of Stationary States

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Abstract

We demonstrate theoretically and numerically that laser-driven many-electron dynamics, as described by bivariational time-dependent coupled-cluster (CC) theory, may be analyzed in terms of stationary-state populations. Projectors heuristically defined from linear response theory and equation-of-motion CC theory are proposed for the calculation of stationary-state populations during interaction with laser pulses or other external forces, and conservation laws of the populations are discussed. Numerical tests of the proposed projectors, involving both linear and nonlinear optical processes for He and Be atoms and for LiH, CH+, and LiF molecules show that the laser-driven evolution of the stationary-state populations at the coupled-cluster singles-and-doubles (CCSD) level is very close to that obtained by full configuration interaction (FCI) theory, provided that all stationary states actively participating in the dynamics are sufficiently well approximated. When double-excited states are important for the dynamics, the quality of the CCSD results deteriorates. Observing that populations computed from the linear response projector may show spurious small-amplitude, high-frequency oscillations, the equation-of-motion projector emerges as the most promising approach to stationary-state populations.

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Pedersen, T. B., Kristiansen, H. E., Bodenstein, T., Kvaal, S., & Schøyen, Ø. S. (2021). Interpretation of Coupled-Cluster Many-Electron Dynamics in Terms of Stationary States. Journal of Chemical Theory and Computation, 17(1), 388–404. https://doi.org/10.1021/acs.jctc.0c00977

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