A theory for colors of strongly correlated electronic systems

Swagata Acharya (), Dimitar Pashov, Cedric Weber, Mark Schilfgaarde, Alexander I. Lichtenstein and Mikhail I. Katsnelson
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Swagata Acharya: Radboud University
Dimitar Pashov: King’s College London
Cedric Weber: The Australian National University
Mark Schilfgaarde: National Renewable Energy Laboratory
Alexander I. Lichtenstein: University of Hamburg
Mikhail I. Katsnelson: Radboud University

Nature Communications, 2023, vol. 14, issue 1, 1-10

Abstract: Abstract Many strongly correlated transition metal insulators are colored, even though they have band gaps much larger than the highest energy photons from the visible light. An adequate explanation for the color requires a theoretical approach able to compute subgap excitons in periodic crystals, reliably and without free parameters—a formidable challenge. The literature often fails to disentangle two important factors: what makes excitons form and what makes them optically bright. We pick two archetypal cases as examples: NiO with green color and MnF2 with pink color, and employ two kinds of ab initio many body Green’s function theories; the first, a perturbative theory based on low-order extensions of the GW approximation, is able to explain the color in NiO, while the same theory is unable to explain why MnF2 is pink. We show its color originates from higher order spin-flip transitions that modify the optical response, which is contained in dynamical mean-field theory (DMFT). We show that symmetry lowering mechanisms may determine how ‘bright’ these excitons are, but they are not fundamental to their existence.

Date: 2023
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DOI: 10.1038/s41467-023-41314-6

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