Enhancement of Exciton-Phonon Scattering from Monolayer to Bilayer WS 2

Layered transition metal dichalcogenides exhibit the emergence of a direct bandgap at the monolayer limit along with pronounced excitonic effects. In these materials, interaction with phonons is the dominant mechanism that limits the exciton coherence lifetime. Exciton-phonon interaction also facili...

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Veröffentlicht in:Nano letters 2018-10, Vol.18 (10), p.6135-6143
Hauptverfasser: Raja, Archana, Selig, Malte, Berghäuser, Gunnar, Yu, Jaeeun, Hill, Heather M, Rigosi, Albert F, Brus, Louis E, Knorr, Andreas, Heinz, Tony F, Malic, Ermin, Chernikov, Alexey
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Sprache:eng
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Zusammenfassung:Layered transition metal dichalcogenides exhibit the emergence of a direct bandgap at the monolayer limit along with pronounced excitonic effects. In these materials, interaction with phonons is the dominant mechanism that limits the exciton coherence lifetime. Exciton-phonon interaction also facilitates energy and momentum relaxation, and influences exciton diffusion under most experimental conditions. However, the fundamental changes in the exciton-phonon interaction are not well understood as the material undergoes the transition from a direct to an indirect bandgap semiconductor. Here, we address this question through optical spectroscopy and microscopic theory. In the experiment, we study room-temperature statistics of the exciton line width for a large number of mono- and bilayer WS samples. We observe a systematic increase in the room-temperature line width of the bilayer compared to the monolayer of 50 meV, corresponding to an additional scattering rate of ∼0.1 fs . We further address both phonon emission and absorption processes by examining the temperature dependence of the width of the exciton resonances. Using a theoretical approach based on many-body formalism, we are able to explain the experimental results and establish a microscopic framework for exciton-phonon interactions that can be applied to naturally occurring and artificially prepared multilayer structures.
ISSN:1530-6984
1530-6992
DOI:10.1021/acs.nanolett.8b01793