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Bulletin of the American Physical Society

Long Time Behavior of Time-Dependent Density Functional Theory

Normand A. Modine, Cheng‐Wei Lee, André Schleife

Published Mar 5, 2018• 0 citations
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arXiv:2403.04458•Physical Review Letters•Dec 23, 2024•1 citation
A long-standing challenge in the time-dependent density functional theory is to efficiently solve the exact time-dependent optimized effective potential (TDOEP) integral equation derived from orbital-dependent functionals, especially for the study of nonadiabatic dynamics in time-dependent external fields. In this Letter, we formulate a completely equivalent time-local TDOEP equation that admits a unique real-time solution in terms of time-dependent Kohn-Sham and effective memory orbitals. The time-local formulation is numerically implemented, with the incorporation of exponential memory loss to address the unaccounted for correlation component in the exact-exchange-only functional, to enable the study of the many-electron dynamics of a one-dimensional hydrogen chain. It is shown that the long time behavior of the electric dipole converges correctly and the zero-force theorem is fulfilled in the current implementation.
Time-dependent density functional theory (TDDFT) is widely used for understanding and predicting properties and behaviors of matter. As one of the fundamental theorems in TDDFT, Van Leeuwen theorem [Phys. Rev. Lett. 82, 3863 (1999)PRLTAO0031-900710.1103/PhysRevLett.82.3863] guarantees how to construct a unique potential with the same one-body density evolution. Here we extend Van Leeuwen theorem by exploring truncation criteria in Bogoliubov-Born-Green-Kirkwood-Yvon (BBGKY) hierarchy. Our generalized theorem demonstrates the existence of a unique nonlocal potential to accurately reconstruct the multibody density evolution in binary interacting systems. Under nonstringent conditions, truncation of the BBGKY-hierarchy equations aligns with the behavior of multibody density evolution and maintains consistency in the reduced equations. Based on this theorem, we further construct a static many-body potential and extend the well-known Casida equation for multiple-excitation energy. The extended TDDFT provides an accurate and first-principles framework capable of describing the kinetic processes of correlated systems, including strongly coupled particle transport, multiple-excitation, and ionization processes.