卤化物
光致发光
纳米晶
发光
钙钛矿(结构)
齿合度
配体(生物化学)
材料科学
相(物质)
胶体
化学
光化学
纳米技术
无机化学
晶体结构
结晶学
光电子学
物理化学
受体
有机化学
生物化学
作者
Rajesh Kumar Gautam,Sumanta Paul,Anunay Samanta
标识
DOI:10.1002/slct.202402890
摘要
Abstract Colloidal cesium lead halide (CsPbX 3 , X = Cl, Br, I) perovskite nanocrystals (NCs) hold promises in photovoltaic and optoelectronic applications. However, their poor long‐term stability results in degradation of optical properties under ambient conditions. Various methods have been explored to address these issues. In this study, we demonstrate that following 3‐precursor hot‐injection method employing ethylenediammonium dihalide (EDAX 2 ) as an additional ligand/halide source one can obtain phase‐pure, monodispersed, stable, and highly luminescent CsPbX 3 NCs. Our violet‐emitting CsPbCl 3 , blue‐emitting CsPbClBr 2 , Green‐emitting CsPbBr 3 , yellow‐emitting CsPbBr 2 I, and red‐emitting CsPbI 3 NCs show PLQYs of 53%, 97%, 96%, 93%, and 95%, respectively. Moreover, the CsPbI 3 NCs, which are known for their phase instability, exhibit stability for up to two months under ambient conditions. The enhanced stability and photoluminescence are attributed to strong binding of the bidentate ligand (EDA 2+ ) to the surface of the NCs and effective removal of the halide‐deficiency trap states by X − .
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