The correlation between phase transition and photoluminescence properties of CsPbX3 (X = Cl, Br, I) perovskite nanocrystals

被引:28
|
作者
Yi, Jun [1 ,2 ]
Ge, Xueying [1 ]
Liu, Exian [1 ,2 ]
Cai, Tong [3 ]
Zhao, Chujun [2 ]
Wen, Shuangchun [2 ]
Sanabria, Hugo [1 ]
Chen, Ou [3 ]
Rao, Apparao M. [1 ]
Gao, Jianbo [1 ]
机构
[1] Clemson Univ, Dept Phys & Astron, Clemson Nanomat Inst, Clemson, SC 29634 USA
[2] Hunan Univ, Hunan Prov Key Lab Low Dimens Struct Phys & Devic, Key Lab Micro Nano Optoelect Devices, Minist Educ,Sch Phys & Elect, Changsha 410082, Peoples R China
[3] Brown Univ, Dept Chem, Providence, RI 02912 USA
来源
NANOSCALE ADVANCES | 2020年 / 2卷 / 10期
关键词
LIGHT-EMITTING-DIODES; HALIDE PEROVSKITES; EMISSION;
D O I
10.1039/d0na00545b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report a correlation between the structural phase transition of CsPbX3 (X = Cl, Br, I) nanocrystals (NCs) and their temperaturedependent steady-state photoluminescence (PL) and time-resolved PL (TRPL). In contrast to CsPbBr3 and CsPbI3 NCs which exhibited a continuous blue-shift in their band gap with increasing temperature, the CsPbCl3 exhibited a blue shift until similar to 193 K, followed by a red shift until room temperature. We attribute this change from a blue to a red shift to a structural phase transition in CsPbCl3, which also manifested in the temperature dependent TRPL. This pronounced phase transition in CsPbCl3 NCs is probably due to the condensation of its vibrational modes at low temperature, and the presence of the weak quantum confinement effect. Notably, the exciton recombination lifetimes showed a similar reverse trend due to the phase transition in CsPbCl3, which has not been reported previously.
引用
收藏
页码:4390 / 4394
页数:5
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