Efficient treatment of molecular excitations in the liquid phase environment via stochastic many-body theory

Accurate predictions of charge excitation energies of molecules in the disordered condensed phase are central to the chemical reactivity, stability, and optoelectronic properties of molecules and critically depend on the specific environment. Herein, we develop a stochastic GW method for calculating these charge excitation energies. The approach employs maximally localized electronic states to define the electronic subspace of a molecule and the rest of the system, both of which are randomly sampled. We test the method on three solute-solvent systems: phenol, thymine, and phenylalanine in water. The results are in excellent agreement with the previous high-level calculations and available experimental data. The stochastic calculations for supercells containing up to 1000 electrons representing the solvated systems are inexpensive and require <= 1000 central processing unit hrs. We find that the coupling with the environment accounts for similar to 40% of the total correlation energy. The solvent-to-solute feedback mechanism incorporated in the molecular correlation term causes up to 0.6 eV destabilization of the quasiparticle energy. Simulated photo-emission spectra exhibit red shifts, state-degeneracy lifting, and lifetime shortening. Our method provides an efficient approach for an accurate study of excitations of large molecules in realistic condensed phase environments.

Automated summary

The study demonstrates the development of a stochastic GW method for accurately calculating charge excitation energies of molecules in realistic condensed phase environments. The method has been validated on solute-solvent systems with results in excellent agreement with high-level calculations and experimental data. The coupling with the environment accounts for approximately 40% of the total correlation energy, leading to destabilization of quasiparticle energy and observable effects in simulated photo-emission spectra.