Band alignments, conduction band edges and intralayer bandgap renormalisation in MoSe 2 /WSe 2 heterobilayers
Stacking two semiconducting transition metal dichalcogenide (MX 2 ) monolayers to form a heterobilayer creates a new variety of semiconductor junction with unique optoelectronic features, such as hosting long-lived dipolar interlayer excitons. Despite many optical, transport, and theoretical studies...
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Veröffentlicht in: | 2d materials 2024-10, Vol.11 (4), p.45021 |
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Hauptverfasser: | , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Stacking two semiconducting transition metal dichalcogenide (MX 2 ) monolayers to form a heterobilayer creates a new variety of semiconductor junction with unique optoelectronic features, such as hosting long-lived dipolar interlayer excitons. Despite many optical, transport, and theoretical studies, there have been few direct electronic structure measurements of these junctions. Here, we apply angle-resolved photoemission spectroscopy with micron-scale spatial resolution ( µ ARPES) to determine the band alignments in MoSe 2 /WSe 2 heterobilayers, using in-situ electrostatic gating to electron-dope and thus probe the conduction band edges. By comparing spectra from heterobilayers with opposite stacking orders, that is, with either MoSe 2 or WSe 2 on top, we confirm that the band alignment is type II, with the valence band maximum in the WSe 2 and the conduction band minimum in the MoSe 2 . The overall band gap is E G = 1.43 ± 0.03 eV, and to within experimental uncertainty it is unaffected by electron doping. However, the offset between the WSe 2 and MoSe 2 valence bands clearly decreases with increasing electron doping, implying band renormalisation only in the MoSe 2 , the layer in which the electrons accumulate. In contrast, µ ARPES spectra from a WS 2 /MoSe 2 heterobilayer indicate type I band alignment, with both band edges in the MoSe 2 . These insights into the doping-dependent band alignments and gaps of MX 2 heterobilayers will be useful for properly understanding and ultimately utilizing their optoelectronic properties. |
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ISSN: | 2053-1583 2053-1583 |
DOI: | 10.1088/2053-1583/ad7b51 |