Electronic Structure and Enhanced Charge-Density Wave Order of Monolayer VSe2

• Published in: Nano letters Vol. 18; no. 7; pp. 4493 - 4499
• Main Authors: Feng, Jiagui, Biswas, Deepnarayan, Rajan, Akhil, Watson, Matthew D, Mazzola, Federico, Clark, Oliver J, Underwood, Kaycee, Marković, Igor, McLaren, Martin, Hunter, Andrew, Burn, David M, Duffy, Liam B, Barua, Sourabh, Balakrishnan, Geetha, Bertran, François, Le Fèvre, Patrick, Kim, Timur K, van der Laan, Gerrit, Hesjedal, Thorsten, Wahl, Peter, King, Phil D. C
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 11-07-2018
• Subjects: VSe2; charge-density wave; monolayer; transition-metal dichalcogenide
• ISSN: 1530-6984; 1530-6992
• DOI: 10.1021/acs.nanolett.8b01649

How the interacting electronic states and phases of layered transition-metal dichalcogenides evolve when thinned to the single-layer limit is a key open question in the study of two-dimensional materials. Here, we use angle-resolved photoemission to investigate the electronic structure of monolayer VSe2 grown on bilayer graphene/SiC. While the global electronic structure is similar to that of bulk VSe2, we show that, for the monolayer, pronounced energy gaps develop over the entire Fermi surface with decreasing temperature below T c = 140 ± 5 K, concomitant with the emergence of charge-order superstructures evident in low-energy electron diffraction. These observations point to a charge-density wave instability in the monolayer that is strongly enhanced over that of the bulk. Moreover, our measurements of both the electronic structure and of X-ray magnetic circular dichroism reveal no signatures of a ferromagnetic ordering, in contrast to the results of a recent experimental study as well as expectations from density functional theory. Our study thus points to a delicate balance that can be realized between competing interacting states and phases in monolayer transition-metal dichalcogenides.