4.8 Article

Boosting the Performance of Self-Powered CsPbCl3-Based UV Photodetectors by a Sequential Vapor-Deposition Strategy and Heterojunction Engineering

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 13, 期 38, 页码 45744-45757

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c15013

关键词

CsPbCl3; vapor deposition; self-powered photodetector; interface modification; image sensing

资金

  1. National Natural Science Foundation of China [51975226, 51905203]

向作者/读者索取更多资源

This study demonstrates a novel sequential vapor-deposition technique to fabricate high-quality CsPbCl3 polycrystalline film for the first time, leading to the construction of a self-powered photodetector with excellent UV detection performance. The device shows fast response time, high on/off ratio, and high responsivity under 375 nm UV illumination. Furthermore, the introduction of a PbS buffer layer improves device performance and stability.
All-inorganic CsPbCl3 perovskite in ultraviolet (UV) detection is drawing increasing interest owing to its UV-matchable optical band gap, ultrahigh UV stability, and superior inherent optoelectronic properties. Almost all of the reported CsPbCl3 photodetectors employ CsPbCl3 nano- or microstructures as sensitive components, while CsPbCl3 polycrystalline film-based self-powered photodetectors are rarely studied on account of the terrible precursor solubility. Herein, a novel sequential vapor-deposition technique is demonstrated to fabricate CsPbCl3 polycrystalline film for the first time. High-quality CsPbCl3 films with excellent optical, electronic, and morphological features are obtained. A self-powered photodetector based on the CsPbCl3 film is constructed without any charge transport layer, showing a high UV detection performance. A thin p-type PbS buffer layer is further introduced to passivate the surface defects of the CsPbCl3 layer and decrease the interfacial energy barrier by forming a type-II heterojunction, contributing to a faster hole extraction rate and a suppressed dark current level. The best-performing device achieves an ultrafast response time of 1.92 mu s, an ultrahigh on/off ratio of 2.22 x 10(5), and a responsivity of 0.22 A/W upon 375 nm UV illumination at 0 V bias. This comprehensive performance is the best among all of the CsPbCl3 photodetectors reported to date. The as-prepared photodetectors also present an eminent UV irradiation and long-term durability in ambient air. Furthermore, a large-area and uniform 625-pixel UV image sensor is fabricated and attains a prominent imaging capability. Our work opens a new avenue for the scalable production of CsPbCl3-based optoelectronics.

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