钝化
卤化物
油胺
极地的
量子点
钙钛矿(结构)
光致发光
水溶液
结晶
化学
化学工程
无机化学
光化学
纳米技术
材料科学
光电子学
有机化学
图层(电子)
纳米颗粒
物理
工程类
天文
作者
Hong Zhu,Yuexiao Pan,Chengdong Peng,Hongzhou Lian,Jun Lin
标识
DOI:10.1002/anie.202116702
摘要
A crucial challenge is to develop an in situ passivation treatment strategy for CsPbX3 (CPX, X=Cl, Br, and I) quantum dots (QDs) and simultaneously retain their luminous efficiency and wavelength. Here, a facile method to significantly improve the stability of the CPX QDs via in situ crystallization with the synergistic effect of 4-bromo-butyric acid (BBA) and oleylamine (OLA) in polar solvents including aqueous solution and a possible fundamental mechanism are proposed. Monodispersed CsPbBr3 (CPB) QDs obtained in water show high photoluminescence quantum yields (PLQYs) of 86.4 % and their PL features of CPB QDs have no significant change after being dispersed in aqueous solution for 96 h, which implies the structure of CPB QDs is unchanged. The results provide a viable design strategy to synthesize all-inorganic perovskite CPX QDs with strong stability against the attack of polar solvents and shed more light on their surface chemistry.
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