Well separated trion and neutral excitons on superacid treated MoS2 monolayers
arXiv:1604.05831 · doi:10.1063/1.4954837
Abstract
Developments in optoelectronics and spin-optronics based on transition metal dichalcogenide monolayers (MLs) need materials with efficient optical emission and well-defined transition energies. In as-exfoliated MoS2 MLs the photoluminescence (PL) spectra even at low temperature consists typically of broad, overlapping contributions from neutral, charged excitons (trions) and localized states. Here we show that in superacid treated MoS2 MLs the PL intensity increases by up to 60 times at room temperature. The neutral and charged exciton transitions are spectrally well separated in PL and reflectivity at T=4 K, with linewidth for the neutral exciton of 15 meV, but with similar intensities compared to the ones in as-exfoliated MLs at the same temperature. Time resolved experiments uncover picoseconds recombination dynamics analyzed separately for charged and neutral exciton emission. Using the chiral interband selection rules, we demonstrate optically induced valley polarization for both complexes and valley coherence for only the neutral exciton.
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- Control of Exciton Valley Coherence in Transition Metal Dichalcogenide Monolayers
- Direct exciton emission from atomically thin transition metal dichalcogenide heterostructures near the lifetime limit
- Optical response of monolayer, few-layer and bulk tungsten disulfide
- Exciton Trapping Is Responsible for the Long Apparent Lifetime in Acid-Treated MoS2
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