Learned free-energy functionals from pair-correlation matching for dynamical density functional theory

Classical density functional theory (cDFT) and dynamical density functional theory (DDFT) are modern statistical mechanical theories for modeling many-body colloidal systems at the one-body density level. The theories hinge on knowing the excess free-energy accurately, which is, however, not feasible for most practical applications. Dijkman et al. [Phys. Rev. Lett. 134, 056103 (2025)0031-900710.1103/PhysRevLett.134.056103] recently showed how a neural excess free-energy functional for cDFT can be learned from bulk simulations via pair-correlation matching. In this article, we demonstrate how this same functional can be applied to DDFT, without any retraining, to simulate nonequilibrium overdamped dynamics of inhomogeneous densities. We evaluate this on a three-dimensional Lennard-Jones system with planar geometry under various complex external potentials, and we observe good agreement of the dynamical densities with those from expensive Brownian dynamic simulations, up to the limit of the adiabatic approximation. We further develop and apply an extension of DDFT based on gradient flows to a grand-canonical system modeled after breakthrough gas adsorption studies, finding similarly good agreement. Our results demonstrate a practical route for leveraging learned free-energy functionals in DDFT, paving the way for accurate and efficient modeling of many-body nonequilibrium systems.