Wafer-Scale Synthesis of WS2 Films with In Situ Controllable p-Type Doping by Atomic Layer Deposition

Author:

Yang Hanjie1ORCID,Wang Yang1,Zou Xingli2,Bai Rongxu1,Wu Zecheng1,Han Sheng1,Chen Tao1,Hu Shen1,Zhu Hao1,Chen Lin1,Zhang David W.1,Lee Jack C.3,Lu Xionggang2,Zhou Peng1,Sun Qingqing1,Yu Edward T.3,Akinwande Deji3ORCID,Ji Li1ORCID

Affiliation:

1. State Key Laboratory of ASIC and System, School of Microelectronics, Fudan University, Shanghai 200433, China

2. State Key Laboratory of Advanced Special Steel, School of Materials Science and Engineering, Shanghai University, Shanghai 200444, China

3. Microelectronics Research Center, Department of Electrical and Computer Engineering, The University of Texas at Austin, Austin, 78758 Texas, USA

Abstract

Wafer-scale synthesis of p-type TMD films is critical for its commercialization in next-generation electro/optoelectronics. In this work, wafer-scale intrinsic n-type WS2 films and in situ Nb-doped p-type WS2 films were synthesized through atomic layer deposition (ALD) on 8-inch α-Al2O3/Si wafers, 2-inch sapphire, and 1 cm2 GaN substrate pieces. The Nb doping concentration was precisely controlled by altering cycle number of Nb precursor and activated by postannealing. WS2 n-FETs and Nb-doped p-FETs with different Nb concentrations have been fabricated using CMOS-compatible processes. X-ray photoelectron spectroscopy, Raman spectroscopy, and Hall measurements confirmed the effective substitutional doping with Nb. The on/off ratio and electron mobility of WS2 n-FET are as high as 105 and 6.85 cm2 V-1 s-1, respectively. In WS2 p-FET with 15-cycle Nb doping, the on/off ratio and hole mobility are 10 and 0.016 cm2 V-1 s-1, respectively. The p-n structure based on n- and p- type WS2 films was proved with a 104 rectifying ratio. The realization of controllable in situ Nb-doped WS2 films paved a way for fabricating wafer-scale complementary WS2 FETs.

Funder

National Natural Science Foundation of China

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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