钙钛矿(结构)
卤化物
二极管
材料科学
激子
光电子学
纳米晶
位阻效应
离子
发光二极管
量子点
量子效率
有机发光二极管
纳米技术
金属
卤素
结晶
无机化学
作者
J Zhang,Tianjun Liu,Qichun Gu,Shuailing Lin,Jian Mao,Zimu Wei,Meng Wang,Yang Lu,Bo Cai,Zher Ying Ooi,Alessandro James Mirabelli,Linyuan Lian,Miguel Anaya,Y Y Liu,Mochen Jia,Xu Chen,Yanbing Han,Xinzhen Ji,Y Zhang,Zhuangzhuang Ma
标识
DOI:10.1038/s41467-026-72733-w
摘要
Abstract Metal halide perovskite light-emitting diodes offer a promising platform for low-cost full-color displays, yet achieving high-performance pure-red emission remains challenging. Here, we report a crystallization regulation strategy for mixed bromide/iodide quasi-two-dimensional perovskites using a multifunctional molecule, 4-(trifluoromethyl)benzenesulfonamide, which simultaneously coordinates with organic spacer cations, Pb 2+ ions and halide ions. Moreover, the combination of large steric hindrance and ordered molecular assembly in the precursor solution plays a decisive role in directing the formation of nanocrystals, thereby suppressing defect formation, inhibiting halide ions migration, and enhancing exciton binding energy. The resulting light-emitting diodes exhibited pure-red emission at ~635 nm, delivering a peak external quantum efficiency of 30.2%, a maximum luminance exceeding 25,000 cd m -2 , and a half-lifetime of 8426 min. Achieving perovskite light-emitting diodes with performance comparable to that of quantum-dot or organic light-emitting diodes would mark a major milestone toward commercialization. This work would expand opportunities beyond conventional light-emitting diode technologies.
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