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Exciton-to-Trion Conversion in Monolayer WS2 under Pressure
Beatrice D'Alò1, Mattia Capeccia1, Lilia Boeri1
1Department of Physics, Sapienza University of Rome, Piazzale Aldo Moro 5, Rome 00185, Italy.
High pressure converts excitons to trions in two-dimensional WS2. This substrate-independent process, driven by crystal compression, shifts emission dominance to charged fermions and offers new avenues for optoelectronics.
Area of Science:
- Condensed Matter Physics
- Materials Science
- Optoelectronics
Background:
- Exciton-to-trion conversion in 2D semiconductors transitions optoelectronics from neutral bosons to charged fermions.
- This conversion impacts transport and spin/valley properties, previously induced via gate voltage, chemical doping, or nanoscale strain.
- Understanding this conversion is key for advanced semiconductor applications.
Purpose of the Study:
- To investigate the evolution of the photoluminescence spectrum of monolayer WS2 under high pressure.
- To decouple exciton and trion contributions by analyzing their responses to laser-power variations.
- To explore pressure-induced exciton-to-trion conversion mechanisms independent of external charge injection.
Main Methods:
- High-pressure photoluminescence spectroscopy of monolayer WS2.
- Analysis of spectral changes with varying laser power to distinguish exciton and trion contributions.
- Application of hydrostatic pressure up to several GPa.
Main Results:
- Crystal compression induces a partially reversible exciton-to-trion conversion in monolayer WS2.
- Trion recombination becomes dominant in photoluminescence emission above 3 GPa.
- The conversion mechanism is substrate-independent and driven by pressure-induced changes in intrinsic doping levels.
Conclusions:
- High pressure can effectively drive exciton-to-trion conversion in 2D materials without external charge injection.
- Modulating interatomic interactions via pressure reshapes the crystal potential, enabling trion-based emission.
- This offers a novel pathway for studying and controlling exciton-trion dynamics in 2D materials for future optoelectronics.
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