Haupttitel:
Spin/Valley Coupled Dynamics of Electrons and Holes at the MoS2–MoSe2 Interface
Autor*in:
Kumar, Abhijeet; Iagodkin, Denis; Stetzuhn, Nele; Kovalchuk, Sviatoslav; Melnikov, Alexey; Elliott, Peter; Sharma, Sangeeta; Gahl, Cornelius; Bolotin, Kirill
Datum der Freigabe:
2022-08-22T04:49:35Z
Abstract:
The coupled spin and valley degrees of freedom in transition metal dichalcogenides (TMDs) are considered a promising platform for information processing. Here, we use a TMD heterostructure MoS2–MoSe2 to study optical pumping of spin/valley polarized carriers across the interface and to elucidate the mechanisms governing their subsequent relaxation. By applying time-resolved Kerr and reflectivity spectroscopies, we find that the photoexcited carriers conserve their spin for both tunneling directions across the interface. Following this, we measure dramatically different spin/valley depolarization rates for electrons and holes, ∼30 and <1 ns–1, respectively, and show that this difference relates to the disparity in the spin–orbit splitting in conduction and valence bands of TMDs. Our work provides insights into the spin/valley dynamics of photoexcited carriers unaffected by complex excitonic processes and establishes TMD heterostructures as generators of spin currents in spin/valleytronic devices.
Teil des Identifiers:
ISSN (print): 1530-6984
e-ISSN (online): 1530-6992
Freie Schlagwörter:
Transition metal dichalcogenides (TMDs)
2-D semiconductor heterostructures
Time-resolved Kerr rotation
Spin/valley dynamics
Opto-spintronics
DDC-Klassifikation:
539 Moderne Physik
Publikationstyp:
Wissenschaftlicher Artikel
Jahrgang/Volume:
21 (2021)
Zeitschrift:
Nano Letters
Verlagsort:
Washington, DC
Fachbereich/Einrichtung:
Physik
Institut für Experimentalphysik
Anmerkungen:
"This document is the Accepted Manuscript version of a Published Work that appeared in final form in Nano Lett., copyright © 2021 American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.nanolett.1c01538."