Journal
NANO LETTERS
Volume 21, Issue 6, Pages 2363-2369Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.nanolett.0c04204
Keywords
Transition metal dichalcogenides; scanning tunneling microscopy; semiconductor heterostructures; strain engineering; wave function hybridization
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Funding
- Center for Novel Pathways to Quantum Coherence in Materials, an Energy Frontier Research Center - U.S. Department of Energy, Office of Science, Basic Energy Sciences
- National Science Foundation through the Cornell Center for Materials Research MRSEC [DMR-1719875]
- University of Chicago MRSEC [DMR-2011854, DMR-1807233]
- Alexander von Humboldt Foundation
- National Science Foundation Graduate Research Fellowship Program [DGE-1746045]
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This study demonstrates that lateral single-layer TMD heterostructures have promising potential for future ultrathin devices with precise structural and electronic properties. Characterization of strain and electronic effects at the heterojunction interface has been explored, showing a reduction in WS2 bandgap due to uniform built-in strain and type-II band alignment with an ultranarrow electronic transition region.
Lateral single-layer transition metal dichalcogenide (TMD) heterostructures are promising building blocks for future ultrathin devices. Recent advances in the growth of coherent heterostructures have improved the structural precision of lateral heterojunctions, but an understanding of the electronic effects of the chemical transition at the interface and associated strain is lacking. Here we present a scanning tunneling microscopy study of single-layer coherent TMD heterostructures with nearly uniform strain on each side of the heterojunction interface. We have characterized the local topography and electronic structure of single-layer WS2/WSe2 heterojunctions exhibiting ultrasharp coherent interfaces. Uniform built-in strain on each side of the interface arising from lattice mismatch results in a reduction of the bandgap of WS2. By mapping the tunneling differential conductance across the interface, we find type-II band alignment and an ultranarrow electronic transition region only similar to 3 nm in width that arises from wave function mixing between the two materials.
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