Exciton dynamics and non-linearities in two-dimensional hybrid organic perovskites

被引:39
作者
Abdel-Baki, K. [1 ]
Boitier, F. [1 ]
Diab, H. [1 ]
Lanty, G. [1 ]
Jemli, K. [1 ]
Ledee, F. [1 ]
Garrot, D. [2 ]
Deleporte, E. [1 ]
Lauret, J. S. [1 ]
机构
[1] Univ Paris Saclay, Univ Paris 11, ENS Cachan, CNRS,Lab Aime Cotton, F-91405 Orsay, France
[2] Univ Paris Saclay, CNRS, UVSQ, GEMAC, 45 Ave Etats Unis, F-78035 Versailles, France
关键词
SOLAR-CELLS; STATES; PHOTOLUMINESCENCE;
D O I
10.1063/1.4941345
中图分类号
O59 [应用物理学];
学科分类号
摘要
Due to their high potentiality for photovoltaic applications or coherent light sources, a renewed interest in hybrid organic perovskites has emerged for few years. When they are arranged in two dimensions, these materials can be considered as hybrid quantum wells. One consequence of the unique structure of 2D hybrid organic perovskites is a huge exciton binding energy that can be tailored through chemical engineering. We present experimental investigations of the exciton non-linearities by means of femtosecond pump-probe spectroscopy. The exciton dynamics is fitted with a bi-exponential decay with a free exciton life-time of similar to 100 ps. Moreover, an ultrafast intraband relaxation (<150 fs) is also reported. Finally, the transient modification of the excitonic line is analyzed through the moment analysis and described in terms of reduction of the oscillator strength and linewidth broadening. We show that excitonic non-linearities in 2D hybrid organic perovskites share some behaviours of inorganic semiconductors despite their high exciton binding energy. (C) 2016 AIP Publishing LLC.
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页数:6
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