Abstract
We present in this contribution the first application of local correlation in the context of multicomponent methods. Multicomponent approaches allow for the targeted simulation of electrons together with other Fermions (most commonly protons) as quantum particles. These methods have become increasingly popular over the last years, particularly for the description of nuclear quantum effects (in strong hydrogen bonds, proton tunneling, and many more). However, most implementations are still based on canonical formulations of wave function theory, which we know for decades to be computationally inefficient for capturing dynamical correlation effects. Local correlation approaches, particularly with the use of pair natural orbitals (PNOs), enable asymptotically linear scaling of computational costs with very little impact on the overall accuracy. In this context, the efficient use of density fitting approximations in the integral calculation proves essential. We start by discussing our implementation of density-fitted NEO-MP2 and NEO-PNO-LMP2, upgrading the electronic correlation treatment up to PNO local coupled cluster level of theory. Several challenging examples are provided to benchmark the method in terms of accuracy as well as computational cost scaling. Following appropriate protocols, anharmonic corrections to localized X-H stretches can be applied routinely with little computational overhead.