Optical spectra and exchange-correlation effects in molecular crystals

TL;DR

This paper uses advanced first-principles calculations to analyze the optical spectra and exchange-correlation effects in molecular crystals, specifically rubrene, revealing the nature of excitons and their impact on optical properties.

Contribution

It provides a detailed first-principles analysis of excitonic effects and exchange interactions in molecular crystals, highlighting the role of many-body effects in optical spectra.

Findings

Intermolecular charge-transfer excitons cause yellow-green photoluminescence.

Spin-triplet excitons are localized with predicted red phosphorescence.

Calculated electronic gap is 2.8 eV, matching experimental data.

Abstract

We report first-principles GW-Bethe Salpeter Equation and Quantum Monte Carlo calculations of the optical and electronic properties of molecular and crystalline rubrene (C$_{42}$H$_{28}$). Many-body effects dominate the optical spectrum and quasi-particle gap of molecular crystals. We interpret the observed yellow-green photoluminescence in rubrene microcrystals as a result of the formation of intermolecular, charge-transfer spin-singlet excitons. In contrast, spin-triplet excitons are localized and intramolecular with a predicted phosphorescence at the red end of the optical spectrum. We find that the exchange energy plays a fundamental role in raising the energy of intramolecular spin-singlet excitons above the intermolecular ones. Exciton binding energies are predicted to be around 0.5 eV (spin singlet) to 1 eV (spin triplet). The calculated electronic gap is 2.8 eV. The theoretical absorption spectrum agrees very well with recent ellipsometry data.