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Metal Contacts on Physical Vapor Deposited Monolayer MoS

Author(s)
Gong, ChengHuang, ChunmingMiller, JustinCheng, LanxiaHao, YufengCobden, DavidKim, JiyoungRuoff, Rodney S.Wallace, Robert M.Cho, KyeongjaeXu, XiaodongChabal, Yves J.
Issued Date
2013-12
DOI
10.1021/nn4052138
URI
https://scholarworks.unist.ac.kr/handle/201301/47499
Fulltext
https://pubs.acs.org/doi/10.1021/nn4052138
Citation
ACS NANO, v.7, no.12, pp.11350 - 11357
Abstract
The understanding of the metal and transition metal dichalcogenide (TMD) interface is critical for future electronic device technologies based on this new class of two-dimensional semiconductors. Here, we investigate the initial growth of nanometer-thick Pd, Au, and Ag films on monolayer MoS2. Distinct growth morphologies are identified by atomic force microscopy: Pd forms a uniform contact, Au clusters into nanostructures, and Ag forms randomly distributed islands on MoS2. The formation of these different interfaces is elucidated by large-scale spin-polarized density functional theory calculations. Using Raman spectroscopy, we find that the interface homogeneity shows characteristic Raman shifts in E-2g(1) and A(1g) modes. Interestingly, we show that insertion of graphene between metal and MoS2 can effectively decouple MoS2 from the perturbations imparted by metal contacts (e.g., strain), while maintaining an effective electronic coupling between metal contact and MoS2, suggesting that graphene can act as a conductive buffer layer in TMD electronics.
Publisher
AMER CHEMICAL SOC
ISSN
1936-0851
Keyword (Author)
molybdenum disulfidemetal contacthomogeneityatomic force microscopyRaman spectroscopygraphenebuffer layer
Keyword
WORK FUNCTIONGRAPHENEGROWTHENERGY

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