We present an approach to parameterize DFT+U+V from hybrid-functional calculations using Wannier-function projections. The method constructs a common localized Wannier basis for both semilocal DFT and hybrid-functional calculations, then determines effective on-site (U) and intersite (V) Hubbard parameters by minimizing the Hamiltonian mismatch within the correlated subspace. This procedure yields interaction parameters that reproduce the hybrid-functional electronic structure at a fraction of the computational cost and allow efficient structural relaxations and further many-body calculations. We validate the workflow on three oxide systems with different electronic characters: MgO (wide-gap insulator), NiO (antiferromagnetic charge-transfer insulator), and V2O5 (d0 transition-metal oxide). In all cases, the mapped DFT+U+V parameters reproduce hybrid-functional band gaps, densities of states, and magnetic moments and improve upon semilocal DFT while maintaining computational efficiency.
@article{arxiv.2602.20814,
title = {Parameterizing DFT+U+V from Hybrid Functionals: A Wannier-Function-Based Approach for Strongly Correlated Materials},
author = {Dmitry M. Korotin and Anna A. Anisimova and Vladimir I. Anisimov},
journal= {arXiv preprint arXiv:2602.20814},
year = {2026}
}