量子点
钙钛矿(结构)
材料科学
光电子学
发光二极管
二极管
纳米技术
化学
结晶学
作者
Xiansheng Li,Hosein Ahangar,Shiyu Yang,Jing Huang,Esmaeil Sheibani,Artem V. Kuklin,Xin Luo,Fatemeh Arami Ghahfarokhi,Changting Wei,Hans Ågren,Glib Baryshnikov,Bo Xu
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-02-11
标识
DOI:10.1021/acsnano.4c11367
摘要
Organic hole-transporting materials (HTMs) with high hole mobility and a defect passivating ability are critical for improving the performance and stability of perovskite optoelectronics, including perovskite quantum dot light-emitting diodes (Pe-QLEDs) and perovskite solar cells. In this study, we designed two small-molecule HTMs, termed X13 and X15, incorporating the methylthio group (SMe) as defect-passivating sites to enhance the interaction between HTMs and the perovskite layer for Pe-QLED applications. Our study highlights that X15, featuring SMe groups at the para-position of the carbazole unit, demonstrates a strong interaction and superior passivation effects with perovskite quantum dots. Consequently, Pe-QLEDs (0.09 cm2) incorporating X15 as the HTM achieve a maximum external quantum efficiency (EQE) of 22.89%. Moreover, employing X15 in large-area Pe-QLEDs (1 cm2) yields an EQE of 21.10% with uniform light emission, surpassing the PTAA-based devices (EQE ∼ 15.03%). Our finding provides crucial insights into the molecular design of defect-passivating small-molecule HTMs for perovskite light-emitting diodes and related optoelectronic devices.
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