We investigate valley dynamics associated with trions in monolayer tungsten diselenide (WSe2) using polarization resolved two-color pump-probe spectroscopy. When tuning the pump and probe energy across the trion resonance, distinct trion valley polarization dynamics are observed as a function of energy and attributed to the intra-valley and inter-valley trions in monolayer WSe2. We observe no decay of a near-unity valley polarization associated with the intra-valley trions during ~ 25 ps, while the valley polarization of the inter-valley trions exhibits a fast decay of ~ 4 ps. Furthermore, we show that resonant excitation is a prerequisite for observing the long-lived valley polarization associated with the intra-valley trion. The exceptionally robust valley polarization associated with resonantly created intra-valley trions discovered here may be explored for future valleytronic applications such as valley Hall effects.Keywords: atomically thin semiconductors, valley, trions, ultrafast dynamics PACS:The valley degree of freedom (DoF) indexes the crystal momentum of a local energy minimum within the electronic band structure, and has been proposed as an alternative information carrier, analogous to charge and spin [1]. In atomically thin transition metal dichalcogenides (TMDs), fundamental optical excitations, excitons (electron-hole pairs) and trions (charged excitons), are formed at the hexagonal Brillouin zone boundaries at the ( ′) points. As such, they inherit the valley index which is locked with electron spins in TMDs. Thus, exciton and trion resonances allow optical access and manipulation of the valley DoF in TMDs using circularly polarized light [2][3][4][5][6]. The exceptionally large binding energies of these quasiparticles (i.e. 200-500 meV for excitons and an additional binding energy of 20-40 meV for trions) further promise room temperature valleytronic applications [2,3,[7][8][9][10][11][12][13].High efficiency valley initialization and a long lifetime of valley polarization are preferred in valleytronic applications [14][15][16][17]. Initial experiments based on steadystate photoluminescence have shown the possibility of creating a near-unity valley polarization in MoS2 and WSe2 via exciton resonances [4,18]. Time-resolved measurements soon revealed that exciton valley polarization is quickly lost (~ 1 ps) due to intrinsic electron-hole exchange interaction [19]. The large initial exciton valley polarization observed in the steady-state PL results from the competition between the valley depolarization time (~ 1 ps) and the exciton population relaxation time (~ 100-200 fs) [13,20,21]. On the other hand, trions offer an interesting alternative route for optical manipulation of the valley index for a number of reasons. First, in contrast to the ultrafast exciton population relaxation time, trions exhibit an extended population relaxation time of tens of picoseconds in monolayer TMDs [22][23][24][25][26][27][28][29][30]. Secondly, trions as charged quasiparticles influence both transport and optical...
We investigate the effect of disorder on exciton valley polarization and valley coherence in monolayer WSe 2 . By analyzing polarization properties of photoluminescence, the valley coherence (VC) and valley polarization (VP) is quantified across the inhomogeneously broadened exciton resonance. We find that disorder plays a critical role in the exciton VC, while affecting VP less. For different monolayer samples with disorder characterized by their Stokes Shift (SS), VC decreases in samples with higher SS while VP does not follow a simple trend. These two methods consistently demonstrate that VC as defined by the degree of linearly polarized photoluminescence is more sensitive to disorder, motivating further theoretical studies.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.