Optical properties of defects in solids via quantum embedding with good active space orbitals

• DOI: 10.48550/arxiv.2301.09668
• Publication Date: 2024-02-13
• Authors: Bryan T. G. Lau; Brian Busemeyer; Timothy C. Berkel...
• Keywords: Chemical Physics (physics.chem-ph); Condensed Matter - Materials Science; Physics - Chemical Physics; 0103 physical sciences; Materials Science (cond-mat.mtrl-sci); FOS: Physical sciences; 01 natural sciences

8 pages, 4 figures<br/>The study of isolated defects in solids is a natural target for classical or quantum embedding methods that treat the defect at a high level of theory and the rest of the solid at a lower level of theory. Here, in the context of active-space-based quantum embeddings, we study the performance of three active-space orbital selection schemes based on canonical (energy-ordered) orbitals, local orbitals defined in the spirit of density matrix embedding theory, and approximate natural transition orbitals. Using equation-of-motion coupled-cluster theory with single and double excitations (CCSD), we apply these active space selection schemes to the calculation of the vertical singlet excitation energy of a substitutional carbon dimer defect in hexagonal boron nitride, an oxygen vacancy in magnesium oxide, and a carbon vacancy in diamond. Especially when used in combination with a simple composite correction, we find that the best performing schemes can predict the excitation energy to about 0.1-0.2 eV of its converged value using only a few hundred orbitals, even when the full supercell has thousands of orbitals, which amounts to many-orders-of-magnitude computational savings when using correlated electronic structure theories. When compared to assigned experimental spectra and accounting for vibrational corrections, we find that CCSD predicts excitation energies that are accurate to about 0.1-0.3 eV, which is comparable to its performance in molecules and bulk solids.<br/>