Engineering the Bandgap and Surface Structure of CsPbCl3 Nanocrystals to Achieve Efficient Ultraviolet Luminescence

被引:52
|
作者
Zhang, Yunqin [1 ,2 ,3 ]
Cheng, Xiyue [1 ,2 ]
Tu, Datao [1 ,2 ,4 ]
Gong, Zhongliang [1 ,2 ]
Li, Renfu [1 ,2 ,4 ]
Yang, Yingjie [1 ,2 ,3 ]
Zheng, Wei [1 ,2 ,4 ]
Xu, Jin [1 ,2 ,4 ]
Deng, Shuiquan [1 ,2 ,3 ,4 ]
Chen, Xueyuan [1 ,2 ,3 ,4 ]
机构
[1] Chinese Acad Sci, Fujian Inst Res Struct Matter, CAS Key Lab Design & Assembly Funct Nanostruct, Fujian Key Lab Nanomat, Fuzhou 350002, Fujian, Peoples R China
[2] Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Fujian, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[4] Fujian Sci & Technol Innovat Lab Optoelect Inform, Fuzhou 350108, Fujian, Peoples R China
关键词
band gap; CsPbCl3; lead halide perovskite nanocrystals; surface passivation; ultraviolet luminescence;
D O I
10.1002/anie.202017370
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Herein, we report the design of novel ultraviolet luminescent CsPbCl3 nanocrystals (NCs) with the emission peak at 381 nm through doping of cadmium ions. Subsequently, a surface passivation strategy with CdCl2 is adopted to improve their photoluminescence quantum yield (PLQY) with the maximum value of 60.5 %, which is 67 times higher than that of the pristine counterparts. The PLQY of the surface passivated NCs remains over 50 % after one week while the pristine NCs show negligible emission. By virtue of density functional theory calculations, we reveal that the higher PLQY and better stability after surface passivation may result from the significant elimination of surface chloride vacancy (V-Cl) defects. These findings provide fundamental insights into the optical manipulation of metal ion-doped CsPbCl3 NCs.
引用
收藏
页码:9693 / 9698
页数:6
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