Abstract
Understanding and controlling the spin degree of freedom in two-dimensional transition metal dichalcogenides offers the potential for designing functional quantum materials. This work investigates the dynamics of photo- and resident carrier spins in an encapsulated MoSe2 monolayer using non-degenerate time-resolved Kerr-rotation microscopy. The lightly doped monolayer exhibits clear exciton and trion resonances with spin-polarizations that are characterized by a fast (~20 ps) decay attributed to photocarrier relaxation and recombination, followed by a slow (~690 ps) decay associated with resident carrier depolarization. Dual-frequency Kerr-rotation spectra directly reveal exciton-trion coupling on ultrashort timescales and within the spin coherence time of the system. Moreover, the distribution of the exciton-trion coupling features exposes inhomogeneous broadening likely arising from different domains within the excitation spot.
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