钙钛矿(结构)
材料科学
成核
钝化
氧化铟锡
光电子学
二极管
铟
发光二极管
激子
量子效率
基质(水族馆)
猝灭(荧光)
氧化物
Crystal(编程语言)
纳米技术
带隙
接口(物质)
离子
磁滞
锡
能量转换效率
化学工程
晶体生长
纳米晶
氧化锡
光致发光
作者
Na Jiang,Guoquan Ma,Dandan Song,Bo Qiao,Zheng Xu,Suling Zhao
标识
DOI:10.1002/adom.202503580
摘要
ABSTRACT Blue perovskite light‐emitting diodes (PeLEDs) are a crucial breakthrough toward practical full‐color displays and solid‐state lighting. However, the widely used hole‐injection material, poly(3,4‐ethylenedioxythiophene): poly(styrenesulfonate) (PEDOT: PSS), exhibits high acidity, a sizable energy‐level mismatch that hampers hole injection, and limited conductivity, which undermines device efficiency and operational stability. Herein, a facile buried interface engineering strategy is proposed to manipulate the nucleation and growth of perovskite films through the incorporation of a multifunctional, zwitterionic potassium taurate (KTAU) into PEDOT: PSS. The K + ions act as heterogeneous nucleation sites, promoting uniform surface coverage and preferred crystal orientation. The electron‐donating group SO 3 − can passivate the buried interface defects by coordinating with undercoordinated Pb 2+ and suppress the nonradiative recombination. In addition, the acid‐base neutralization eliminates the In species release from the indium tin oxide substrate, inhibiting exciton quenching at the PEDOT: PSS/perovskite interface. By reorganizing the molecular conformation of PEDOT: PSS, KTAU boosts PEDOT‐rich domains, improving band alignment of the perovskite layer. Benefiting from these synergistic effects, KTAU‐modified blue PeLEDs deliver a maximum external quantum efficiency (EQE) of 7.33%—3.1 × higher than the control one, together with prolonged operational lifetime. The results establish a grain‐growth substrate strategy for efficient and stable blue PeLEDs.
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