硫
配体(生物化学)
溴化物
齿合度
热稳定性
量子产额
钙钛矿(结构)
纳米晶
化学
光化学
四唑
高分子化学
材料科学
无机化学
物理化学
有机化学
纳米技术
盐(化学)
荧光
晶体结构
受体
物理
量子力学
生物化学
作者
Yuting Cai,Wenbo Li,Dongjie Tian,Shuchen Shi,Xi Chen,Peng Gao,Rong‐Jun Xie
标识
DOI:10.1002/anie.202209880
摘要
Abstract Herein, we report a new X‐type ligand, i.e., organic sulfonium bromide, for high‐efficiency CsPbBr 3 and MAPbBr 3 (MA=methylammonium) perovskite nanocrystals (PNCs). We first confirmed the facile synthesis of the titled ligands in N,N‐dimethylformamide at room temperature. By reacting dodecylmethylsulfide with allyl bromide, (3‐bromopropyl)trimethoxysilane, and 1,4‐dibromobutane, respectively, three representative ligands (named DAM, DSM, and DMM) are acquired. All of them result in CsPbBr 3 and MAPbBr 3 PNCs with near‐unity photoluminescence quantum yield (PLQY) and decent ambient stability (no less than 90 % PLQY after 2 months) using a room‐temperature ligand‐assisted reprecipitation technique. Among them, DSM and DMM endow CsPbBr 3 PNCs with higher thermal/light stability arising from the cross‐linkable or bidentate ligand structure. Further, DSM‐CsPbBr 3 PNCs can be incorporated into polystyrene through in situ thermal polymerization and the composite shows a record‐high PLQY of 93.8 %.
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