Publications by authors named "J TOULOUSE"

Article Synopsis
  • The research introduces a real-time, time-dependent approach to analyze high-harmonic generation (HHG) signals in molecules by focusing on individual molecular orbital (MO) contributions.
  • It utilizes the time-dependent Schrödinger equation with complex energies to account for ionization and employs specialized Gaussian basis sets for calculating high-energy states.
  • The findings reveal how MO contributions correlate with laser pulse symmetries, affecting the HHG spectra of CO2 and H2O, and provide insights into the roles of different orbitals based on laser polarization directions.
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Using GPU-accelerated state-vector emulation, we propose to embed a quantum computing ansatz into density-functional theory via density-based basis-set corrections to obtain quantitative quantum-chemistry results on molecules that would otherwise require brute-force quantum calculations using hundreds of logical qubits. Indeed, accessing a quantitative description of chemical systems while minimizing quantum resources is an essential challenge given the limited qubit capabilities of current quantum processors. We provide a shortcut towards chemically accurate quantum computations by approaching the complete-basis-set limit through coupling the density-based basis-set corrections approach, applied to any given variational ansatz, to an on-the-fly crafting of basis sets specifically adapted to a given system and user-defined qubit budget.

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We present the first application to real molecular systems of the recently proposed linear-response theory for the density-based basis-set correction method [, , 234107 (2023)]. We apply this approach to accelerate the basis-set convergence of excitation energies in the equation-of-motion coupled-cluster singles and doubles (EOM-CCSD) method. We use an approximate linear-response framework that neglects the second-order derivative of the basis-set correction density functional and consists in simply adding to the usual Hamiltonian the one-electron potential generated by the first-order derivative of the functional.

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This work reports an efficient density-fitting implementation of the density-based basis-set correction (DBBSC) method in the MOLPRO software. This method consists in correcting the energy calculated by a wave-function method with a given basis set by an adapted basis-set correction density functional incorporating the short-range electron correlation effects missing in the basis set, resulting in an accelerated convergence to the complete-basis-set limit. Different basis-set correction density-functional approximations are explored and the complementary-auxiliary-basis-set single-excitation correction is added.

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Background And Objective: Patients with presumed nonlesional focal epilepsy-based on either MRI or histopathologic findings-have a lower success rate of epilepsy surgery compared with lesional patients. In this study, we aimed to characterize a large group of patients with focal epilepsy who underwent epilepsy surgery despite a normal MRI and had no lesion on histopathology. Determinants of their postoperative seizure outcomes were further studied.

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