化学
钙钛矿(结构)
量子点
发光二极管
钝化
电致发光
成核
二极管
光电子学
量子效率
纳米晶
荧光粉
俄歇效应
发光
纳米技术
材料科学
结晶学
螺旋钻
物理
图层(电子)
原子物理学
有机化学
作者
Yuan Liu,Yitong Dong,Tong Zhu,Dongxin Ma,Andrew H. Proppe,Bin Chen,Chao Zheng,Yi Hou,Seungjin Lee,Bin Sun,Eui Hyuk Jung,Fanglong Yuan,Ya‐Kun Wang,Laxmi Kishore Sagar,Sjoerd Hoogland,F. Pelayo Garcı́a de Arquer,Min‐Jae Choi,Kamalpreet Singh,Shana O. Kelley,Oleksandr Voznyy,Zheng‐Hong Lu,Edward H. Sargent
摘要
Light-emitting diodes (LEDs) based on metal halide perovskite quantum dots (QDs) have achieved impressive external quantum efficiencies; however, the lack of surface protection of QDs, combined with efficiency droop, decreases device operating lifetime at brightnesses of interest. The epitaxial incorporation of QDs within a semiconducting shell provides surface passivation and exciton confinement. Achieving this goal in the case of perovskite QDs remains an unsolved challenge in view of the materials' chemical instability. Here, we report perovskite QDs that remain stable in a thin layer of precursor solution of perovskite, and we use strained QDs as nucleation centers to drive the homogeneous crystallization of a perovskite matrix. Type-I band alignment ensures that the QDs are charge acceptors and radiative emitters. The new materials show suppressed Auger bi-excition recombination and bright luminescence at high excitation (600 W cm–2), whereas control materials exhibit severe bleaching. Primary red LEDs based on the new materials show an external quantum efficiency of 18%, and these retain high performance to brightnesses exceeding 4700 cd m–2. The new materials enable LEDs having an operating half-life of 2400 h at an initial luminance of 100 cd m–2, representing a 100-fold enhancement relative to the best primary red perovskite LEDs.
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