Ballistic transport spectroscopy of spin-orbit-coupled bands in monolayer graphene on WSe2

Van der Waals interactions with transition metal dichalcogenides were shown to induce strong spin-orbit coupling (SOC) in graphene, offering great promises to combine large experimental flexibility of graphene with unique tuning capabilities of the SOC. Here, we probe SOC-driven band splitting and e...

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Veröffentlicht in:Nature communications 2023-09, Vol.14 (1), p.6124-6124, Article 6124
Hauptverfasser: Rao, Qing, Kang, Wun-Hao, Xue, Hongxia, Ye, Ziqing, Feng, Xuemeng, Watanabe, Kenji, Taniguchi, Takashi, Wang, Ning, Liu, Ming-Hao, Ki, Dong-Keun
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Sprache:eng
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Zusammenfassung:Van der Waals interactions with transition metal dichalcogenides were shown to induce strong spin-orbit coupling (SOC) in graphene, offering great promises to combine large experimental flexibility of graphene with unique tuning capabilities of the SOC. Here, we probe SOC-driven band splitting and electron dynamics in graphene on WSe 2 by measuring ballistic transverse magnetic focusing. We found a clear splitting in the first focusing peak whose evolution in charge density and magnetic field is well reproduced by calculations using the SOC strength of ~ 13 meV, and no splitting in the second peak that indicates stronger Rashba SOC. Possible suppression of electron-electron scatterings was found in temperature dependence measurement. Further, we found that Shubnikov-de Haas oscillations exhibit a weaker band splitting, suggesting that it probes different electron dynamics, calling for a new theory. Our study demonstrates an interesting possibility to exploit ballistic electron motion pronounced in graphene for emerging spin-orbitronics. By combining graphene with transition metal dichalcogenides, such as WSe2, it is possible to induce a large spin-orbit interaction in the graphene layer. Here, Rao et al study the spin-orbit coupling in graphene/WSe2 heterostructures using the ballistic transport based technique, known transverse magnetic focusing.
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-023-41826-1