Observation of quantum-confined exciton states in monolayer WS quantum dots by ultrafast spectroscopy.

Monolayer transition metal dichalcogenide quantum dots (TMDC QDs) could exhibit unique photophysical properties, because of both lateral quantum confinement effect and edge effect. However, there is little fundamental study on the quantum-confined exciton dynamics in monolayer TMDC QDs, to date. Here, by selective excitations of monolayer WS QDs in broadband transient absorption (TA) spectroscopy experiments, the excitation-wavelength-dependent ground state bleaching signals corresponding to the quantum-confined exciton states are directly observed. Compared to the time-resolved photophysical properties of WS nanosheets, the selected monolayer WS QDs only show one ground state bleaching peak with larger initial values for the linear polarization anisotropy of band-edge excitons, probably due to the expired spin-orbit coupling. This suggests a complete change of the band structure for monolayer WS QDs. In the femtosecond time-resolved circular polarization anisotropy experiments, a valley depolarization time of ∼100 fs is observed for WS nanosheets at room temperature, which is not observed for monolayer WS QDs. Our findings suggest a strong state-mixing of band-edge valley excitons responsible for the large linear polarization in monolayer WS QDs, which could be helpful for understanding the exciton relaxation mechanisms in colloidal monolayer TMDC QDs.