The linear absorption spectra in monolayers of transition metal dichalcogenides show pronounced signatures of the exceptionally strong exciton-phonon interaction in these materials. To account for both exciton and phonon physics in such optical signals, we compare different theoretical methods to calculate the absorption spectra using the example of MoSe2. In this paper, we derive the equations of motion for the polarization either using a correlation expansion up to 4th Born approximation or a time convolutionless master equation. We show that the Born approximation might become problematic when not treated in high enough order, especially at high temperatures. In contrast, the time convolutionless formulation gives surprisingly good results despite its simplicity when compared to higher-order corrrelation expansion and therefore provides a powerful tool to calculate the lineshape of linear absorption spectra in the very popular monolayer materials.
Transition metal dichalcogenide monolayers have attracted wide attention due to their remarkable optical, electronic and mechanical properties. In these materials local strain distributions effectively form quasi zero-dimensional potentials, whose localized states may be populated by carrier capture from the continuum states. Using a recently developed Lindblad single-particle approach, here we study the phonon-induced carrier capture in a MoSe2 monolayer. Although one decisive control parameter is the energy selection rule, which links the energy of the incoming carriers to that of the final state via the emitted phonon, we show that additionally the spatio-temporal dynamics plays a crucial role. By varying the direction of the incoming carriers with respect to the orientation of the localized potential, we introduce a new control mechanism for the carrier capture: the spatial control.
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