Systematic improvement of molecular excited state calculations by inclusion of nuclear quantum motion: a mode-resolved picture and the effect of molecular size

Abstract

The energies of molecular excited states arise as solutions to the electronic Schrödinger equation and are often compared to experiment. At the same time, nuclear quantum motion is known to be important and to induce a red-shift of excited state energies. However, it is thus far unclear whether incorporating nuclear quantum motion in molecular excited state calculations leads to a systematic improvement of their predictive accuracy, making further investigation necessary. Here we present such an investigation by employing two first-principles methods for capturing the effect of quantum fluctuations on excited state energies, which we apply to the Thiel set of organic molecules. We show that accounting for zero-point motion leads to much improved agreement with experiment, compared to `static' calculations which only account for electronic effects, and the magnitude of the red-shift can become as large as 1.36 eV. Moreover, we show that the effect of nuclear quantum motion on excited state energies largely depends on the molecular size, with smaller molecules exhibiting larger red-shifts. Our methodology also makes it possible to analyze the contribution of individual vibrational normal modes to the red-shift of excited state energies, and in several molecules we identify a limited number of modes dominating this effect. Overall, our study provides a foundation for systematically quantifying the shift of excited state energies due to nuclear quantum motion, and for understanding this effect at a microscopic level.

References in corpus (5)

• NWChem: Past, Present, and Future
• An assessment of the low-lying excitation energies and triplet instabilities of organic molecules with an ab initio Bethe-Salpeter equation approach
• Vibrational averages along thermal lines
• The impact of exciton delocalization on exciton-vibration interactions in organic semiconductors
• XDFT: an efficient first-principles method for neutral excitations in molecules

Cited by in corpus (3)

• Inverse molecular design from first principles: tailoring organic chromophore spectra for optoelectronic applications
• ExROPPP: Fast, Accurate and Spin-Pure Calculation of the Electronically Excited States of Organic Hydrocarbon Radicals
• Theory of ab initio downfolding with arbitrary range electron-phonon coupling