This work demonstrates improved accuracy in modeling strongly correlated systems using DMRG-in-DFT embedding, indicating better chemical predictions.
The projection-based wave function in density functional theory (WF-in-DFT) embedding enables an efficient description of both the energetics and properties of large and complex chemical systems, with accuracy exceeding that of pure DFT. Recently, we have proposed using the density matrix renormalization group (DMRG) as the WF method for molecules containing strongly correlated fragments [Beran, P. J. Phys. Chem. Lett. 2023, 14, 716-722]. In this work, we demonstrate that the accuracy of the DMRG-in-DFT approach is primarily limited by the approximate treatment of the coupling between the active component and its environment through nonadditive exchange-correlation functionals. To address this issue, we combine exact exchange to reduce the nonadditive exchange error with a multireference adiabatic connection (AC) scheme to recover nonadditive correlation. The performance of the improved DMRG-in-DFT embedding is illustrated on two prototypical strongly correlated systems: the dissociation of the H₂₀ chain and the cleavage of a triple CN bond in propionitrile.
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Monino et al. (2026) studied this question.
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