钝化
纳米晶
钙钛矿(结构)
光致发光
二极管
发光二极管
材料科学
氯
发光
光电子学
离子
量子效率
光化学
化学
纳米技术
结晶学
冶金
有机化学
图层(电子)
作者
Le Ma,Xiansheng Li,Xiaoming Li,Jizhong Song,Yingyi Nong,Jing Huang,Changting Wei,Wen‐Hua Zhang,Bo Xu
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-02-26
卷期号:9 (3): 1210-1218
被引量:11
标识
DOI:10.1021/acsenergylett.4c00109
摘要
Mixed Br/Cl-perovskite nanocrystals (Pe-NCs) CsPbBrxCl3–x, synthesized at room temperature (RT), offer several advantages for use in light-emitting diodes (LEDs), including cost-effective processing and a narrow luminescence peak. However, achieving efficient pure blue LEDs using CsPbBrxCl3–x NCs has been proven to be challenging due to a significant number of chlorine defects. In this work, we propose a passivation strategy utilizing hydrazine cations (Hz2+) to eliminate chlorine defects in RT-synthesized Pe-NCs. Our investigation reveals that Hz2+ can capture the isolated chlorine anion (Cl–) to form a Hz–Cl–Cs bridge on the Pe-NC surface, thereby effectively inhibiting the formation of chlorine vacancies. This approach significantly enhances both the photoluminescence efficiency and lifetime of Pe-NCs. Consequently, LEDs fabricated using Hz2+-passivated Pe-NCs achieve an outstanding external quantum efficiency (EQE) of 7.82% at 475 nm. Our findings highlight an effective passivation strategy that significantly mitigates chlorine defects in Pe-NCs, thereby advancing the development of efficient pure blue LEDs.
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