Abstract

To reduce Schottky-barrier-induced contact and access resistance, and the impact of charged impurity and phonon scattering on mobility in devices based on 2D transition metal dichalcogenides (TMDs), considerable effort has been put into exploring various doping techniques and dielectric engineering using high−κhigh-κ oxides, respectively. The goal of this work is to demonstrate a high−κhigh-κ dielectric that serves as an effective n-type charge transfer dopant on monolayer (ML) molybdenum disulfide (MoS2MoS_{2}). Utilizing amorphous titanium suboxide (ATO) as the 'high−κhigh-κ dopant', we achieved a contact resistance of ~ 180180 Ω.μmΩ.μm which is the lowest reported value for ML MoS2MoS_{2}. An ON current as high as 240240 μA/μmμA/μm and field effect mobility as high as 8383 cm2/V−scm^2/V-s were realized using this doping technique. Moreover, intrinsic mobility as high as 102102 cm2/V−scm^2/V-s at 300300 KK and 501501 cm2/V−scm^2/V-s at 7777 KK were achieved after ATO encapsulation which are among the highest mobility values reported on ML MoS2MoS_{2}. We also analyzed the doping effect of ATO films on ML MoS2MoS_{2}, a phenomenon which is absent when stoichiometric TiO2TiO_{2} is used, using ab initio density functional theory (DFT) calculations which shows excellent agreement with our experimental findings. Based on the interfacial-oxygen-vacancy mediated doping as seen in the case of high−κhigh-κ ATO - ML MoS2MoS_{2}, we propose a mechanism for the mobility enhancement effect observed in TMD-based devices after encapsulation in a high−κhigh-κ dielectric environment.

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