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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Rostami, Habib
University of Bath
in Cooperation with on an Cooperation-Score of 37%
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Publications (7/7 displayed)
- 2019Transient hot electron dynamics in single-layer TaS2citations
- 2019Transient hot electron dynamics in single-layer TaS2citations
- 2019Hot electrons modulation of third harmonic generation in graphene
- 2019Exciton routing in the heterostructure of a transition metal dichalcogenide monolayer on a paraelectric substratecitations
- 2019Transient hot electron dynamics in single-layer TaS 2citations
- 2019Transient hot electron dynamics in single-layer TaS 2citations
- 2015Theory of strain in single-layer transition metal dichalcogenidescitations
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article
Transient hot electron dynamics in single-layer TaS2
Abstract
<p>Using time- and angle-resolved photoemission spectroscopy, we study the response of metallic single-layer TaS2 in the 1H structural modification to the generation of excited carriers by a femtosecond laser pulse. A complex interplay of band structure modifications and electronic temperature increase is observed and analyzed by direct fits of model spectral functions to the two-dimensional (energy and k-dependent) photoemission data. Upon excitation, the partially occupied valence band is found to shift to higher binding energies by up to ≈100meV, accompanied by electronic temperatures exceeding 3000 K. These observations are explained by a combination of temperature-induced shifts of the chemical potential, as well as temperature-induced changes in static screening. Both contributions are evaluated in a semiempirical tight-binding model. The shift resulting from a change in the chemical potential is found to be dominant.</p>