磷化氢
材料科学
胺气处理
对偶(语法数字)
光电子学
纳米技术
有机化学
文学类
艺术
催化作用
化学
作者
Jianxin Deng,Zi-Feng Zhang,Yangyang Bian,Qian Li,Wanying Yang,Fei Chen,Huaibin Shen
标识
DOI:10.1002/adfm.202521226
摘要
Abstract Indium phosphide (InP)‐based quantum dots (QDs) have emerged as highly‐promising, environmentally friendly emitting materials for displays. However, the commonly used phosphorus precursor, tris(trimethylsilyl)phosphine ((TMS) 3 P), is expensive, flammable, and explosive, hindering its commercialization. Although tris(dimethylamino)phosphine ((DMA) 3 P) offers a more economical alternative, the resulting QDs and quantum dot light‐emitting diodes (QLEDs) have low performance because of core surface traps and ligand instability. In this study, a dual‐surface treatment strategy is developed that combines NH 4 PF 6 pre‐treatment of InP cores and OT‐based shell growth. First, NH 4 PF 6 is employed to passivate the In/P dangling bonds and remove the oxidation defects, thereby improving size uniformity. Then, 1‐octanethiol (OT) served as both sulfur source and short‐chain ligand to enhance QD stability. The optimized QDs exhibit a near‐unity photoluminescence quantum yield (PL QY) of 96% and exceptional stability, retaining 98% of their initial PL QY after 1 month in ambient air. Moreover, the OT ligand facilitates an elevated energy‐level alignment, reducing the hole injection barrier and boosting radiative recombination. As a result, the OT‐based red QLEDs achieve a record external quantum efficiency (EQE) of 21.55%, maximum luminance of 95,327 cd m −2 , and long T 50 lifetime (time for the luminance to drop to half of the initial value) of 50,066 h, setting a new state‐of‐the‐art performance for (DMA) 3 P‐based QLEDs.
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