Issue 33, 2017, Issue in Progress

Temperature-dependence studies of organolead halide perovskite-based metal/semiconductor/metal photodetectors

Abstract

In this paper, polycrystalline perovskite (CH3NH3PbIxCl3−x) photodetectors with a structure of Au/CH3NH3PbIxCl3−x/Au are prepared and are shown to have good performance. The measured electrical parameters demonstrate that the current behavior of the perovskite photodetectors is dependent of work temperature from 300 K to 350 K. We find that only space charge limited conduction mechanism fits the current–voltage (IV) curves under small external voltage (0.1–0.7 V) both under darkness and illumination. The lattice vibration scattering plays the major role in the dark, leading to a decreased current as the temperature increases under the same external voltage, and an enlarged current increasing with the temperature is due to the leading role of the ionized impurity scattering. At each temperature, the rising slope of the IV curves decrease with the increase of voltage both under dark and illumination. The values of on/off ratio, responsivity and detectivity increase with the measured temperature, which indicates that the polycrystalline perovskite photodetector can work with better performance at high temperature. However, the stability in the dark gradually becomes weak as the temperature increases, especially at 330 K and above.

Graphical abstract: Temperature-dependence studies of organolead halide perovskite-based metal/semiconductor/metal photodetectors

Supplementary files

Article information

Article type
Paper
Submitted
06 Feb 2017
Accepted
03 Apr 2017
First published
07 Apr 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 20206-20211

Temperature-dependence studies of organolead halide perovskite-based metal/semiconductor/metal photodetectors

Y. Wang, Y. Zhang, Y. Liu, T. Pang, Z. Hu, Y. Zhu, S. Luan and R. Jia, RSC Adv., 2017, 7, 20206 DOI: 10.1039/C7RA01496A

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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