Local Potential Functional Embedding Theory of Molecular Systems: Localized Orbital-Based Embedding from an Exact Density-Functional Perspective

Abstract

Localized orbital-based quantum embedding, as originally formulated in the context of density matrix embedding theory (DMET), is revisited from the perspective of lattice density functional theory (DFT). An in-principle exact (in the sense of full configuration interaction) formulation of the theory, where the occupations of the localized orbitals play the role of the density, is derived for any (model or ab initio) electronic Hamiltonian. From this general formalism we deduce an exact relation between the local Hartree-exchange-correlation (Hxc) potential of the full-size Kohn-Sham (KS) lattice-like system and the embedding chemical potential that is adjusted on each embedded fragment, individually, such that both KS and embedding cluster systems reproduce the exact same local density. When well-identified density-functional approximations (that find their justification in the strongly correlated regime) are applied, a practical self-consistent local potential functional embedding theory (LPFET), where the local Hxc potential becomes the basic variable, naturally emerges from the theory. LPFET differs from previous density embedding approaches by its fragment-dependent embedding chemical potential expression, which is a simple functional of the Hxc potential. Numerical calculations on prototypical systems show the ability of such an ansatz to improve substantially the description of density profiles (localized orbitals occupation numbers in this context) in strongly correlated systems.