钙钛矿(结构)
量子点
材料科学
卤化物
离子
降级(电信)
碘化物
光电子学
发光二极管
化学工程
纳米技术
无机化学
化学
计算机科学
电信
有机化学
工程类
作者
Hanleem Lee,Cuc Kim Trinh,Mo Geun So,Chang‐Lyoul Lee
出处
期刊:Nanoscale
[The Royal Society of Chemistry]
日期:2021-12-29
卷期号:14 (9): 3425-3440
被引量:13
摘要
Perovskite quantum dots (QDs) have been extensively studied as emissive materials for next-generation optoelectronics due to their outstanding optical properties; however, their structural instabilities, specifically those of red perovskite QDs, are critical obstacles in realizing operationally reliable perovskite QD-based optoelectronic devices. Accordingly, herein, we investigated the sequential degradation mechanism of red perovskite QDs upon their exposure to an electric field. Via electrical and chemical characterization, we demonstrated that degradation occurred in the following order: anion-defect-assisted halide migration, cation-defect-assisted migration of I-/Cs+ ions, defective gradient I ion distribution, structural distortion, and ion transport/I2 vaporization with defect proliferation. Among these steps, the defective gradient I ion distribution is the key process in the structural degradation of perovskite QDs. Based on our findings, we designed perovskite/SiO2 core-shell QDs with stable gradient I concentrations. Most notably, the operational stabilities of perovskite QD-light-emitting diodes (PeLEDs) fabricated using the perovskite/SiO2 core-shell QDs were approximately 5000 times those of the PeLEDs constructed using pristine perovskite QDs.
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