钙钛矿(结构)
光电效应
量子点
材料科学
配体(生物化学)
理论(学习稳定性)
纳米技术
光电子学
化学物理
化学工程
物理
计算机科学
化学
工程类
机器学习
受体
生物化学
作者
Xuyang Li,Qihang Lv,Zitong Xu,Weijun Wang,Zhixin Tang,Xia Shen,Zhaohui Shan,Yanqin Miao,Johnny C. Ho,Pengfei Guo
标识
DOI:10.1002/adom.202502489
摘要
Abstract Perovskite quantum dots (PeQDs) have attracted significant attention as research materials due to their adjustable bandgaps, high photoluminescence quantum yield, and excellent color purity. However, conventional surface ligands often suffer from weak coordination capacity and low conductivity, adversely affecting the stability and photoelectric properties of PeQDs. In this study, a synergistic ligand pair exchange strategy is introduced to enhance the properties of pristine CsPbBr 3 PeQDs. By sequentially incorporating α ‐methyl‐4‐fluoro‐benzylamine and p ‐toluenesulfonic acid, the original OA/OAm ligand pair is successfully replaced, efficiently passivating the A‐ and X‐site vacancies. The modified CsPbBr 3 PeQDs demonstrate notable improvements in photoluminescence intensity and stability when exposed to UV light, high temperatures, and water immersion. Furthermore, this treatment approach is applicable to CsPbI 3 and mixed‐halogen PeQDs. A high‐performance photodetector fabricated from these treated CsPbBr 3 QDs showcases a responsivity of 3.9 mA W −1 and a detectivity of 2.0 × 10 10 Jones, representing a 6‐fold enhancement over untreated counterparts. Also, devices based on treated CsPbBr 3 QDs show potential in optical communications, effectively illustrating encryption and decryption processes. This synergetic ligand pair exchange strategy offers a promising avenue for the broader application of PeQDs in optoelectronics devices and circuits.
科研通智能强力驱动
Strongly Powered by AbleSci AI