材料科学
成核
结晶
钙钛矿(结构)
均质化(气候)
量子效率
二极管
发光二极管
光电子学
化学工程
纳米技术
热力学
生物多样性
生态学
生物
工程类
物理
作者
Yu Xia,Jiacheng Li,Zhipeng Zhang,Nan Li,Y. A. Wang,Yu‐Han Li,Kai‐Li Wang,Chun‐Hao Chen,Jing Chen,Lei Huang,Yutong Yang,Guichuan Xing,Baoquan Sun,Zhao‐Kui Wang
标识
DOI:10.1002/adma.202506413
摘要
Abstract Conventional antisolvent dripping methods face fundamental limitations in controlling crystallization kinetics, particularly manifesting as instantaneous nucleation and severe spatial inhomogeneity in scaled‐up perovskite films. Herein, a microdroplet‐phase antisolvent deposition technique is developed that establishes a controlled crystallization environment through delayed nucleation kinetics via mild antisolvent interaction and uniform microdroplet diffusion across extended substrates. The resulting small‐area (0.1 cm 2 ) device attains an external quantum efficiency (EQE) of 30.98% at 515 nm, ranking among the best‐performing green perovskite light‐emitting diodes (PeLEDs). A remarkable EQE of 23.21% is also realized when the active area expands to 6.25 cm 2 . This work provides a fundamental advancement in perovskite crystallization control and demonstrates a viable pathway toward industrial‐scale production of PeLEDs.
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