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Lee M. Thompson

Publications and source records attributed to Lee M. Thompson.

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Resolving Peak Shifting Effects in Real-Time Time-Dependent Orbital Propagation Methods Through Nonorthogonal Expansions

Self-consistent field real-time electronic structure methods are a powerful approach for modeling ultrafast processes but suffer from systematic errors in predicted transition energies, commonly known as peak shifting, that obscure direct comparison with experiment. Although this effect has been explored in single reference methods, a general understanding that extends to multiconfigurational methods remains unresolved. Here, we develop a real-time nonorthogonal multiconfigurational self-consistent field (RT-TD NOMCSCF) formalism in which independently propagated orbital sets generate a compact, nonorthogonal wavefunction. The approach establishes a unified framework for nonlinear real-time electronic structure theories, which we use to reveal the common origin of peak shifting across single and multireference limits. Using this framework, we demonstrate that peak shifting does not arise exclusively from the effect of state averaging over the internal space basis, but also from the accessible external configurational space. By systematically expanding the internal space with independently propagated orbital sets, RT-TD NOMCSCF suppresses this aver- aging, recovers correct transition energies, and distinguishes intrinsic peak shifting from numerical peak drifting caused by propagation errors. Thus, these developments establish nonlinear real-time electronic structure methods that enables more accurate simulations of ultrafast processes.

physics.chem-ph

Natural Excitation Framework for Defining the External Space: Uncontracted and Internally Contracted Multireference Nonorthogonal Wavefunction Theories

In this communication, we examine new formalisms for the construction of the external space when correlating reference wavefunctions built from nonorthogonal determinant expansions. Defining the external space in nonorthogonal approaches is challenging, as every substitution from the reference wavefunction can potentially mix both internal and external configurations. As a result, post-nonorthogonal methods are plagued by internal contamination and linear dependencies in the external space, which may lead to correlation double counting that results from overlap of the external and reference spaces. Removal of these internal configurations and orthonormalization of the excited space basis can be computationally expensive. In particular, as the excitation operators cannot be subdivided by their action on orbital subspaces, the external space cannot be partitioned into non-overlapping subsets as is possible in orthogonal methods. To resolve these issues, we propose both uncontracted and internally-contracted approaches based on a natural excitation framework that allows for reduced scaling, more straightforward separation of excitation types that lead to external and internal spaces, and allows for a facile translation of orthogonal methods to a nonorthogonal framework. Several proofs and a numerical demonstration using vanadium monohydride (VH) are provided to illustrate the viability of the proposed approach, using a method-agnostic presentation to highlight the generality of the approach.

physics.chem-ph