Floquet engineering of strongly driven excitons in monolayer tungsten disulfide
Interactions of quantum materials with strong laser fields can induce exotic non-equilibrium electronic states 1 – 6 . Monolayer transition metal dichalcogenides, a new class of direct-gap semiconductors with prominent quantum confinement 7 , offer exceptional opportunities for the Floquet engineeri...
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Veröffentlicht in: | Nature physics 2023-02, Vol.19 (2), p.171-176 |
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Sprache: | eng |
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Zusammenfassung: | Interactions of quantum materials with strong laser fields can induce exotic non-equilibrium electronic states
1
–
6
. Monolayer transition metal dichalcogenides, a new class of direct-gap semiconductors with prominent quantum confinement
7
, offer exceptional opportunities for the Floquet engineering of excitons, which are quasiparticle electron–hole correlated states
8
. Strong-field driving has the potential to achieve enhanced control of the electronic band structure and thus the possibility of opening a new realm of exciton light–matter interactions. However, a full characterization of strong-field driven exciton dynamics
4
,
9
has been difficult. Here we use mid-infrared laser pulses below the optical bandgap to excite monolayer tungsten disulfide and demonstrate strong-field light dressing of excitons in excess of a hundred millielectronvolts. Our high-sensitivity transient absorption spectroscopy further reveals the formation of a virtual absorption feature below the 1
s
-exciton resonance, which we assign to a light-dressed sideband from the dark 2
p
-exciton state. Quantum-mechanical simulations substantiate the experimental results and enable us to retrieve real-space movies of the exciton dynamics. This study advances our understanding of the exciton dynamics in the strong-field regime, showing the possibility of harnessing ultrafast, strong-field phenomena in device applications of two-dimensional materials.
The interaction of strong laser fields with tungsten disulfide leads to light-dressed Floquet replica of excitonic states, which manifest as new features in the transient absorption spectrum. |
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ISSN: | 1745-2473 1745-2481 |
DOI: | 10.1038/s41567-022-01849-9 |