TY - JOUR
T1 - Density-Functionalized QM/MM Delivers Chemical Accuracy For Solvated Systems
AU - Chen, Xin
AU - Martinez B, Jessica A.
AU - Shao, Xuecheng
AU - Riera Riambau, Marc
AU - Andreussi, Oliviero
AU - Paesani, Francesco
AU - Pavanello, Michele
N1 - Publisher Copyright:
© 2025 The Authors. Published by American Chemical Society
PY - 2025/10/28
Y1 - 2025/10/28
N2 - We present a reformulation of QM/MM as a fully quantum mechanical theory of interacting subsystems, all treated at the level of density functional theory (DFT). For the MM subsystem, which lacks orbitals, we assign an ad hoc electron density and apply orbital-free DFT functionals to describe its quantum properties. The interaction between the QM and MM subsystems is also treated using orbital-free density functionals, accounting for Coulomb interactions, exchange, correlation, and Pauli repulsion. Consistency across QM and MM subsystems is ensured by employing data-driven, many-body MM force fields that faithfully represent DFT functionals. Applications to water-solvated systems demonstrate that this approach achieves unprecedented, very rapid convergence to chemical accuracy as the size of the QM subsystem increases. We validate the method with several pilot studies, including water bulk, water clusters (prism hexamer and pentamers), solvated glucose, a palladium aqua ion, and a wet monolayer of MoS2.
AB - We present a reformulation of QM/MM as a fully quantum mechanical theory of interacting subsystems, all treated at the level of density functional theory (DFT). For the MM subsystem, which lacks orbitals, we assign an ad hoc electron density and apply orbital-free DFT functionals to describe its quantum properties. The interaction between the QM and MM subsystems is also treated using orbital-free density functionals, accounting for Coulomb interactions, exchange, correlation, and Pauli repulsion. Consistency across QM and MM subsystems is ensured by employing data-driven, many-body MM force fields that faithfully represent DFT functionals. Applications to water-solvated systems demonstrate that this approach achieves unprecedented, very rapid convergence to chemical accuracy as the size of the QM subsystem increases. We validate the method with several pilot studies, including water bulk, water clusters (prism hexamer and pentamers), solvated glucose, a palladium aqua ion, and a wet monolayer of MoS2.
UR - https://www.scopus.com/pages/publications/105019943985
U2 - 10.1021/acs.jctc.5c01440
DO - 10.1021/acs.jctc.5c01440
M3 - Article
C2 - 41091510
AN - SCOPUS:105019943985
SN - 1549-9618
VL - 21
SP - 10340
EP - 10352
JO - Journal of Chemical Theory and Computation
JF - Journal of Chemical Theory and Computation
IS - 20
ER -