Unlocking of Schottky Barrier Near the Junction of MoS2 Heterostructure Under Electrochemical Potential

Author:

Aydin Kubra12ORCID,Kim Mansu3ORCID,Seok Hyunho12,Bae Chulwoo12,Lee Jinhyoung45,Kim Muyoung367ORCID,Park Jonghwan6,Hupp Joseph T.3ORCID,Whang Dongmok6ORCID,Kim Hyeong‐U78ORCID,Kim Taesung1249ORCID

Affiliation:

1. SKKU Advanced Institute of Nanotechnology (SAINT) Sungkyunkwan University Suwon 16419 Korea

2. Department of Nano Science and Technology Sungkyunkwan University Suwon 16419 Korea

3. Department of Chemistry Northwestern University Evanston Illinois 60208 USA

4. School of Mechanical Engineering Sungkyunkwan University Suwon 16419 Korea

5. Center for Quantum Nanoscience Institute for Basic Science (IBS) Seoul 03760 Korea

6. School of Advanced Material Science and Engineering Sungkyunkwan University Suwon 16419 Korea

7. Semiconductor Manufacturing Research Center Korea Institute of Machinery and Materials (KIMM) Daejeon 34103 Korea

8. Nano‐Mechatronics University of Science & Technology (UST) Daejeon 34113 Korea

9. Department of Nano Engineering Sungkyunkwan University Suwon 16419 Korea

Abstract

The exploration of heterostructures composed of two‐dimensional (2D) transition metal dichalcogenide (TMDc) materials has garnered significant research attention due to the distinctive properties of each individual component and their phase‐dependent unique properties. Using the plasma‐enhanced chemical vapor deposition (PECVD) method, we analyze the fabrication of heterostructures consisting of two phases of molybdenum disulfide (MoS2) in four different cases. The initial hydrogen evolution reaction (HER) polarization curve indicates that the activity of the heterostructure MoS2 is consistent with that of the underlying MoS2, rather than the surface activity of the upper MoS2. This behavior can be attributed to the presence of Schottky barriers, which include contact resistance, which significantly hampers the efficient charge transfer at junctions between the two different phases of MoS2 layers and is mediated by van der Waals bonds. Remarkably, the energy barrier at the junction dissipates upon reaching a certain electrochemical potential, indicating surface activation from the top phase of MoS2 in the heterostructure. Notably, the 1T/2H MoS2 heterostructure demonstrates enhanced electrochemical stability compared to its metastable 1T‐MoS2. This fundamental understanding paves the way for the creation of phase‐controllable heterostructures through an experimentally viable PECVD, offering significant promise for a wide range of applications.

Funder

Northwestern University

Korea Institute of Machinery and Materials

Korea Evaluation Institute of Industrial Technology

National Research Foundation of Korea

Publisher

Wiley

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