Long-living nonlinear behavior in CsPbBr3 carrier recombination dynamics

被引:17
作者
Gabelloni, Fabio [1 ]
Biccari, Francesco [1 ,2 ]
Falsini, Naomi [1 ]
Calisi, Nicola [4 ]
Caporali, Stefano [4 ]
Vinattieri, Anna [1 ,2 ,3 ]
机构
[1] Univ Firenze, Dipartimento Fis & Astron, Via G Sansone 1, I-50019 Sesto Fiorentino, Italy
[2] LENS, Via N Carrara 1, I-50019 Sesto Fiorentino, Italy
[3] Ist Nazl Fis Nucl, Sez Firenze, Via G Sansone 1, I-50019 Sesto Fiorentino, Italy
[4] Univ Firenze, Dipartimento Ingn Ind, Via Santa Marta 3, I-50139 Florence, Italy
关键词
inorganic perovskites; CsPbBr3; time-resolved optical spectroscopy; excitons; thermalization; non-linearity; PEROVSKITE SOLAR-CELLS; HOT-ELECTRONS; NANOCRYSTALS; STABILITY; EMISSION; EXCITONS;
D O I
10.1515/nanoph-2019-0013
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
By means of time-resolved photoluminescence (TR-PL) spectroscopy, we present a detailed investigation of the carrier relaxation dynamics in a CsPbBr3 bulk sample and microcrystal ensemble at cryogenic temperature on a picosecond time scale. We provide evidence of a long temperature-dependent cooling rate for the excitons and free carriers population, with an initial cooling time constant of a few tens of picoseconds. A relaxation bottleneck in the thermalization process was found that cannot be explained by the Auger effect or hot phonon population, since we address a very low excitation regime, not commonly investigated in literature, where such processes are not effective. Adding a continuous wave optical bias to the picosecond excitation, we probed the photoinduced PL decrease of the localized states and the photoinduced PL increase of the population in the high energy states. A long recovery time from the photoinduced PL decrease was found for localized states and quite significant differences were detected, depending on the resonance/off resonance bias used in the experiment.
引用
收藏
页码:1447 / 1455
页数:9
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