Graphene–PbS Quantum Dot Heterostructure for Broadband Photodetector with Enhanced Sensitivity

Author:

Qing Jincheng1,Wang Shicai2,Gu Shuyi1ORCID,Lin Lin2,Xie Qinpei1,Li Daming1,Huang Wen2,Guo Junxiong134ORCID

Affiliation:

1. School of Electronic Information and Electrical Engineering, Institute of Advanced Study, Chengdu University, Chengdu 610106, China

2. School of Integrated Circuit Science and Engineering (Exemplary School of Microelectronics), University of Electronic Science and Technology of China, Chengdu 611731, China

3. School of Materials and Energy, University of Electronic Science and Technology of China, Chengdu 610054, China

4. Chengdu Research Institute of UESTC, Chengdu 610207, China

Abstract

Photodetectors converting light into electrical signals are crucial in various applications. The pursuit of high-performance photodetectors with high sensitivity and broad spectral range simultaneously has always been challenging in conventional semiconductor materials. Graphene, with its zero bandgap and high electron mobility, is an attractive candidate, but its low light absorption coefficient restricts its practical application in light detection. Integrating graphene with light-absorbing materials like PbS quantum dots (QDs) can potentially enhance its photodetection capabilities. Here, this work presents a broadband photodetector with enhanced sensitivity based on a graphene–PbS QD heterostructure. The device leverages the high carrier mobility of graphene and the strong light absorption of PbS QDs, achieving a wide detection range from ultraviolet to near-infrared. Employing a simple spinning method, the heterostructure demonstrates ultrahigh responsivity up to the order of 107 A/W and a specific detectivity on the order of 1013 Jones, showcasing significant potential for photoelectric applications.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Sichuan Province

China Postdoctoral Science Foundation

Key R&D Program of Sichuan Province

Publisher

MDPI AG

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