Microscopically-based energy density functionals for nuclei using the density matrix expansion: Full optimization and validation

Abstract

We seek to obtain a usable form of the nuclear energy density functional that is rooted in the modern theory of nuclear forces. We thus consider a functional obtained from the density matrix expansion of local nuclear potentials from chiral effective field theory. We propose a parametrization of this functional carefully calibrated and validated on selected ground-state properties that is suitable for large-scale calculations of nuclear properties. The first component of this functional is a non-local functional of the density and corresponds to the direct part (Hartree term) of the expectation value of local chiral potentials on a Slater determinant. A second component is a local functional of the density and is obtained by applying the density matrix expansion to the exchange part (Fock term) of the expectation value of the local chiral potential. We apply the UNEDF2 optimization protocol to determine the coupling constants of this energy functional. We obtain a set of microscopically-constrained functionals for local chiral potentials from leading-order up to next-to-next-to-leading order with and without three-body forces and contributions from $Δ$ excitations. These functionals are validated on the calculation of nuclear and neutron matter, nuclear mass tables, single-particle shell structure in closed-shell nuclei and the fission barrier of $^{240}$Pu. Quantitatively, they perform noticeable better than the more phenomenological Skyrme functionals. The inclusion of higher-order terms in the chiral perturbation expansion seems to produce a systematic improvement in predicting nuclear binding energies. This result is especially promising since all the fits have been performed at the single reference level of the energy density functional approach, where important collective correlations such as center-of-mass correction have not been taken into account yet.