Charge transfer in transition metal dichalcogenide alloy heterostructures

F Fangying Ren (Key Laboratory of Luminescence and Optical Information, Ministry of Education, Institute of Optoelectronic Technology, Beijing Jiaotong University 1 , Beijing 100044,) D Dawei He X Xiaoxian Zhang (National Engineering Research Center for Biomaterials, College of Biomedical Engineering, Sichuan University) G Guili Li (Key Laboratory of Luminescence and Optical Information, Ministry of Education, Institute of Optoelectronic Technology, Beijing Jiaotong University 1 , Beijing 100044,) X Xiaojing Liu (Department of Molecular and Structural Biochemistry) J Jiarong Wang (Department of Materials Science and Engineering) K Kun Zhao J Jiaqi He (Shanghai Key Laboratory of New Drug Design, School of Pharmacy, East China University of Science and Technology) Y Yongsheng Wang (Division of Thoracic Tumor Multimodality Treatment Cancer Center, West China Hospital, Sichuan University) H Hui Zhao (Center of Ionic Liquid and Green Energy, Beijing Key Laboratory of Solid State Battery and Energy Storage Process, State Key Laboratory of Mesoscience and Engineering, Institute of Process Engineering)

Abstract

Two-dimensional (2D) transition metal dichalcogenides and their alloys provide a unique platform for exploring interlayer charge transfer in van der Waals heterostructures. These structures are crucial for advancing the next-generation electronic, optoelectronic, and quantum devices. In this study, interlayer charge transfer in heterostructures composed of MoSe2, MoS2, and their alloy, MoSSe, is investigated using transient absorption, Raman, and photoluminescence spectroscopy. The experimental results reveal that electron transfer in the alloy heterostructures, MoSSe/MoS2 and MoSe2/MoSSe, is faster than in the pure MoSe2/MoS2 heterostructure, despite the smaller conduction band offsets of the alloy systems. Raman spectroscopy confirms that alloy layers support phonon modes matching those of the pure layers, aligning with theoretical models of phonon-assisted interlayer charge transfer. Additionally, efficient hole transfer is observed in both alloy heterostructures. The findings suggest transition metal dichalcogenides alloys can be used for engineering heterostructures with desired charge transfer properties. By leveraging compositionally tunable band gaps and optical properties, alloy-based heterostructures offer opportunities for designing tailored materials suitable for diverse applications such as photodetectors, light-emitting devices, and flexible electronics. Moreover, the ultrafast charge transfer observed in these systems provides insights into the fundamental mechanisms governing interlayer interactions in 2D materials.

Article Details

Volume / Issue Vol. 126, Issue 7
Published February 17, 2025
ISSN 0003-6951
Publisher American Institute of Physics

Journal Info

Applied Physics Letters

American Institute of Physics

ISSN: 0003-6951 Physical Sciences

Authors (10)

F

Fangying Ren

Key Laboratory of Luminescence and Optical Information, Ministry of Education, Institute of Optoelectronic Technology, Beijing Jiaotong University 1 , Beijing 100044,

D

Dawei He

X

Xiaoxian Zhang

National Engineering Research Center for Biomaterials, College of Biomedical Engineering, Sichuan University

G

Guili Li

Key Laboratory of Luminescence and Optical Information, Ministry of Education, Institute of Optoelectronic Technology, Beijing Jiaotong University 1 , Beijing 100044,

X

Xiaojing Liu

Department of Molecular and Structural Biochemistry

J

Jiarong Wang

Department of Materials Science and Engineering

K

Kun Zhao

J

Jiaqi He

Shanghai Key Laboratory of New Drug Design, School of Pharmacy, East China University of Science and Technology

Y

Yongsheng Wang

Division of Thoracic Tumor Multimodality Treatment Cancer Center, West China Hospital, Sichuan University

H

Hui Zhao

Center of Ionic Liquid and Green Energy, Beijing Key Laboratory of Solid State Battery and Energy Storage Process, State Key Laboratory of Mesoscience and Engineering, Institute of Process Engineering