Hot-carrier tunable abnormal nonlinear absorption conversion in quasi-2D perovskite

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作者
Gang Wang
Tanghao Liu
Bingzhe Wang
Hao Gu
Qi Wei
Zhipeng Zhang
Jun He
Mingjie Li
Guichuan Xing
机构
[1] Avenida da Universidade,Joint Key Laboratory of the Ministry of Education, Institute of Applied Physics and Materials Engineering, University of Macau
[2] Hong Kong Baptist University,Department of Physics
[3] The Hong Kong Polytechnic University,Department of Applied Physics
[4] Central South University,Hunan Key Laboratory of Nanophotonics and Devices
[5] The Hong Kong Polytechnic University,Photonics Research Institute
[6] Hung Hom,undefined
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摘要
Controlling the high-power laser transmittance is built on the diverse manipulation of multiple nonlinear absorption (NLA) processes in the nonlinear optical (NLO) materials. According to standard saturable absorption (SA) and reverse saturable absorption (RSA) model adapted for traditional semiconductor materials, the coexistence of SA and RSA will result in SA induced transparency at low laser intensity, yet switch to RSA with pump fluence increasing. Here, we observed, in contrast, an unusual RSA to SA conversion in quasi-two-dimensional (2D) perovskite film with a low threshold around 2.6 GW cm−2. With ultrafast transient absorption (TA) spectra measurement, such abnormal NLA is attributed to the competition between excitonic absorption enhancement and non-thermalized carrier induced bleaching. TA singularity from non-thermalized “Fermi Sea” is observed in quasi-2D perovskite film, indicating an ultrafast carrier thermalization within 100 fs. Moreover, the comparative study between the 2D and 3D perovskites uncovers the crucial role of hot-carrier effect to tune the NLA response. The ultrafast carrier cooling of quasi-2D perovskite is pointed out as an important factor to realize such abnormal NLA conversion process. These results provide fresh insights into the NLA mechanisms in low-dimensional perovskites, which may pave a promising way to diversify the NLO material applications.
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