Stable Red Light-Emitting Devices Based on Cd:CsMnBr3 With High Photoluminescence Quantum Yield via Cd Incorporation

发光二极管 量子产额 电致发光 钙钛矿(结构) 光致发光 卤化物 光电子学 材料科学 化学 物理 荧光 纳米技术 光学 无机化学 结晶学 图层(电子)
作者
Yong Ma,Xiaodong Zhang,Hongyan Qiu,Jing Guo,Chao Tian,Liqiang Zheng,Chong Shen
出处
期刊:IEEE Transactions on Electron Devices [Institute of Electrical and Electronics Engineers]
卷期号:70 (11): 5751-5756
标识
DOI:10.1109/ted.2023.3314579
摘要

At present, great success has been achieved in the development of perovskite light-emitting devices (LEDs) with red, green, blue, and near-infrared emission. However, red perovskite LEDs, as a key optoelectronic device, are still challenging, principally because under high bias voltage, halide separation will inevitably occur in mixed halide perovskite, resulting in unwanted color changes of the device. In addition, the poor stability and inherent toxicity of traditional lead halide perovskite limit its practical application. Here, the manufacturing of stable red LEDs based on ternary manganese halide CsMnBr3 is reported, which solves the problems of color instability and lead toxicity faced by perovskite red LEDs. The quantum efficiency is effectively improved by Cd $^{{2}+}$ ion doping. Photoluminescence (PL) quantum yield (PLQY) reaches 73.1% and has long-term stability. It can be stored at room temperature in air for more than 300 days. In addition, the red electroluminescent LEDs prepared with Cd:CsMnBr3 nanocrystals (NCs) has the broadband emission of self-trapping excitons centered at 660 nm and a comparable and reasonable low carrier valid mass conducive to charge transmission. The maximum brightness of the prepared red LEDs is 46.2 cd/ $\text{m}^{{2}}$ , showing a long half-life of 90 min at 25 °C, which is due to the excellent heat resistance, moisture resistance and high temperature resistance of Cd:CsMnBr3, as well as oxidation under environmental conditions. The results show that the broadband and stable emission of Cd:CsMnBr3 is compatible with the practical application of LEDs.
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