Variational Calculations of the Excited States of the Charged NV-center in Diamond Using a Hybrid Functional

TL;DR

This paper uses a hybrid density functional and variational optimization to accurately calculate the excited states of the NV-center in diamond, improving upon previous methods and aiding quantum technology applications.

Contribution

It introduces a variational approach with hybrid functionals for excited state calculations of NV-centers, achieving high accuracy and better agreement with experiments.

Findings

Triplet excited state energy within 0.1 eV of experimental values

Singlet state relaxation energy estimated at 0.06 eV

Method improves upon local and semi-local functional results

Abstract

The excited electronic states involved in the optical cycle preparation of a pure spin state of the negatively charged NV-defect in diamond are calculated using the HSE06 hybrid density functional and variational optimization of the orbitals. This includes the energy of the excited triplet as well as the two lowest singlet states with respect to the ground triplet state. In addition to the vertical excitation, the effect of structural relaxation is also estimated using analytical atomic forces. The lowering of the energy in the triplet excited state and the resulting zero-phonon line triplet excitation energy are both within 0.1 eV of the experimental estimates. An analogous relaxation in the lower energy singlet state using spin purified atomic forces is estimated to be 0.06 eV. These results, obtained with a hybrid density functional, improve on previously published results using local and semi-local functionals, which are known to underestimate the band gap. The good agreement with experimental estimates demonstrates how time-independent variational calculations of excited states using density functionals can give accurate results and, thereby, provide a powerful screening tool for identifying other defect systems as candidates for quantum technologies.