Issue 12, 2024

Suppression of the dark current in PbS quantum dot infrared photodetectors through the introduction of a CuInSeS interfacial layer

Abstract

Lead sulfide (PbS) colloidal quantum dot (CQD) materials are extensively utilized in the fabrication of near-infrared detectors. Advanced PbS quantum dot infrared detectors often employ ligand exchange processes to enhance the performance of the active layer. This process involves the replacement of long-chain ligands, which exhibit poor conductivity, with short-chain ligands, such as 1,2-ethanedithiol (EDT) in the treatment of PbS. However, conventional solid-state ligand exchange techniques are prone to cause inherent cracking, resulting in significant leakage currents that limit detector sensitivity. To address this challenge, we introduce a copper indium selenium sulfur (CuInSeS) quantum dot interfacial layer, resulting in the creation of a smooth and crack-free film. This method effectively optimizes the interfacial contact between PbS and ZnO. Additionally, this layer concurrently establishes a gradient energy level, facilitating the transport of charge carriers. This results in a decrease in the dark current to 4.6 × 10−8 mA under a −1 V bias, achieving a detectivity of 1.87 × 1012 Jones. The results demonstrate that the quantum dot interfacial layer effectively suppresses the dark current of the detector, addressing the deficiencies associated with the solid-state ligand exchange technique. This work provides a direction for further research on detectors.

Graphical abstract: Suppression of the dark current in PbS quantum dot infrared photodetectors through the introduction of a CuInSeS interfacial layer

Supplementary files

Article information

Article type
Paper
Submitted
22 Dec 2023
Accepted
22 Feb 2024
First published
07 Mar 2024

J. Mater. Chem. C, 2024,12, 4493-4500

Suppression of the dark current in PbS quantum dot infrared photodetectors through the introduction of a CuInSeS interfacial layer

Z. Chen, T. Huang, B. Zhang, C. Wu, X. Zhang, T. Sun, W. Xu, K. Kang, C. Xiang, T. Zhang and R. Li, J. Mater. Chem. C, 2024, 12, 4493 DOI: 10.1039/D3TC04746F

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