Journal
PHYSICAL REVIEW B
Volume 96, Issue 8, Pages -Publisher
AMER PHYSICAL SOC
DOI: 10.1103/PhysRevB.96.085302
Keywords
-
Funding
- ERC [306719]
- ITN Spin-NANO Marie Sklodowska-Curie [676108]
- LIA ILNACS CNRS-Ioffe Programme Investissements d'Avenir [ANR-11-IDEX-0002-02, ANR-10-LABX-0037-NEXT]
- MEXT, Japan
- JSPS KAKENHI [JP26248061, JP15K21722, JP25106006]
- Russian Science Foundation [14-12-01067]
- ANR MoS2ValleyControl
- Russian Science Foundation [17-12-00030] Funding Source: Russian Science Foundation
- Grants-in-Aid for Scientific Research [25107004] Funding Source: KAKEN
Ask authors/readers for more resources
Charged excitons, or X-+/- trions, in monolayer transition-metal dichalcogenides have binding energies of several tens of meV. Together with the neutral exciton X-0 they dominate the emission spectrum at low and elevated temperatures. We use charge-tunable devices based on WSe2 monolayers encapsulated in hexagonal boron nitride to investigate the difference in binding energy between X+ and X- and the X- fine structure. We find in the charge-neutral regime, the X-0 emission accompanied at lower energy by a strong peak close to the longitudinal optical (LO) phonon energy. This peak is absent in reflectivity measurements, where only the X-0 and an excited state of the X-0 are visible. In the n-doped regime, we find a closer correspondence between emission and reflectivity as the trion transition with a well-resolved fine-structure splitting of 6 meV for X- is observed. We present a symmetry analysis of the different X+ and X- trion states and results of the binding energy calculations. We compare the trion binding energy for the n- and p-doped regimes with our model calculations for low carrier concentrations. We demonstrate that the splitting between the X+ and X- trions as well as the fine structure of the X(-)state can be related to the short-range Coulomb-exchange interaction between the charge carriers.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available