Coherent dynamics and mapping of excitons in single-layer MoSe2 and WSe2 at the homogeneous limit

Coherent dynamics and mapping of excitons in single-layer MoSe2 and WSe2 at the homogeneous limit

Článek WoS

We perform coherent nonlinear spectroscopy of excitons in single-layers of MoSe2 and WSe2 encapsulated between thin films of hexagonal boron nitride. Employing four-wave-mixing microscopy we identify virtually disorder-free areas, generating an exciton optical response at the homogeneous limit. Focussing on such areas, we measure exciton homogeneous broadening as a function of environmental factors, namely temperature and exciton density. Exploiting four-wave-mixing imaging, we find that at such locations, nonlinear absorption of the exciton excited states and their coherent couplings can be observed. Using the WSe2 heterostructure, we infer coherence and density dynamics of the exciton 2S state. Owing to its increased radiative lifetime, at low temperatures, the dephasing of the 2S state is longer than of the 1S transition. While scanning various heterostructures across tens of micrometers, we conclude that the disorder, principally induced by strain variations, remain to be present creating spatially varying inhomogeneous broadening.

We perform coherent nonlinear spectroscopy of excitons in single-layers of MoSe2 and WSe2 encapsulated between thin films of hexagonal boron nitride. Employing four-wave-mixing microscopy we identify virtually disorder-free areas, generating an exciton optical response at the homogeneous limit. Focussing on such areas, we measure exciton homogeneous broadening as a function of environmental factors, namely temperature and exciton density. Exploiting four-wave-mixing imaging, we find that at such locations, nonlinear absorption of the exciton excited states and their coherent couplings can be observed. Using the WSe2 heterostructure, we infer coherence and density dynamics of the exciton 2S state. Owing to its increased radiative lifetime, at low temperatures, the dephasing of the 2S state is longer than of the 1S transition. While scanning various heterostructures across tens of micrometers, we conclude that the disorder, principally induced by strain variations, remain to be present creating spatially varying inhomogeneous broadening.

SPECTROSCOPY

SPECTROSCOPY

BOULE, C.; VÁCLAVKOVÁ, D.; BARTOŠ, M.; NOGAJEWSKI, K.; ZDRAŽIL, L.; TANIGUCHI, T.; WATANABE, K.; POTEMSKI, M.; KASPRZAK, J.

2021

09.03.2020

2475-9953

Physical Review Materials

4

3

Spojené státy americké

034001-1

034001-8

8

https://journals.aps.org/prmaterials/abstract/10.1103/PhysRevMaterials.4.034001