Reduced density matrix dynamics in multistate harmonic models via time-convolution and time-convolutionless quantum master equations with quantum-mechanical and semiclassical kernels.

In this work, we explore the electronic reduced density matrix (RDM) dynamics using time-convolution (TC) and time-convolutionless (TCL) quantum master equations (QMEs) that are based on perturbative electronic couplings within the framework of multistate harmonic (MSH) models. The MSH model Hamiltonian consistently incorporates the electronic-vibrational correlations between all pairs of states by satisfying the pairwise reorganization energies directly obtained from all-atom simulations, representing the globally heterogeneous environments that couple to the multiple states differently. We derive the exact quantum-mechanical and a hierarchy of semiclassical approximate expressions for the kernels in TC and TCL QMEs that project the full RDM for general shifted harmonic systems, including the MSH model. These QMEs are applied to simulate RDM dynamics of photoinduced charge transfer (PICT) in organic photovoltaic carotenoid-porphyrin-fullerene triad solvated in tetrahydrofuran solution and the excitation energy transfer (EET) dynamics in photosynthetic Fenna-Matthews-Olson complexes from C. tepidum and P. aestuarii. Our results show that while both TC and TCL QMEs capture similar phenomena in PICT and EET processes, TC QME generally provides more accurate results than TCL QME, particularly in the initial oscillation of EET population dynamics. This study highlights the effectiveness of the TC and TCL QMEs in modeling RDM dynamics of nonadiabatic processes, offering insights for realistic condensed phase systems.