Wavefunction matching for solving quantum many-body problems.

Ab initio calculations have an essential role in our fundamental understanding of quantum many-body systems across many subfields, from strongly correlated fermions to quantum chemistry and from atomic and molecular systems to nuclear physics. One of the primary challenges is to perform accurate calculations for systems where the interactions may be complicated and difficult for the chosen computational method to handle. Here we address the problem by introducing an approach called wavefunction matching.

Ab Initio Calculation of the Alpha-Particle Monopole Transition Form Factor.

We present a parameter-free ab initio calculation of the α-particle monopole transition form factor in the framework of nuclear lattice effective field theory. We use a minimal nuclear interaction that was previously used to reproduce the ground state properties of light nuclei, medium-mass nuclei, and neutron matter simultaneously with no more than a few percent error in the energies and charge radii. The results for the monopole transition form factor are in good agreement with recent precision data from Mainz.

Emergent geometry and duality in the carbon nucleus.

The carbon atom provides the backbone for the complex organic chemistry composing the building blocks of life. The physics of the carbon nucleus in its predominant isotope, C, is similarly full of multifaceted complexity. Here we provide a model-independent density map of the geometry of the nuclear states of C using the ab initio framework of nuclear lattice effective field theory.

Harmonic Potential Theorem: Extension to Spin-, Velocity-, and Density-Dependent Interactions.

One of the few exact results for the description of the time evolution of an inhomogeneous, interacting many-particle system is given by the harmonic potential theorem (HPT). The relevance of this theorem is that it sets a tight constraint on time-dependent many-body approximations. In this contribution, we show that the original formulation of the HPT is valid also for the case of spin-, velocity-, and density-dependent interactions.