光探测
激子
钙钛矿(结构)
材料科学
光电子学
光致发光
光电探测器
宽带
化学物理
纳米技术
光学
凝聚态物理
物理
化学
结晶学
作者
Gefei Li,Yong Zhang,Wenhui Wang,Lei Gao,Yukun Ren,Junyan Che,Chunjing Mo,Hongwei Liu,Weijie Zhao,Junpeng Lü,Zhenhua Ni
标识
DOI:10.1002/adom.202200223
摘要
Abstract Self‐trapped excitons (STEs) exert a profound impact on the optical properties and device applications of 2D halide perovskites. Particularly distinct exciton self‐trapping and detrapping processes can facilitate the intelligent design of perovskite optoelectronic devices with emerging functionalities. Thus, a comprehensive understanding and regulation of exciton trapping and detrapping dynamics are highly desired. Herein, the authors report a 2D lead halide perovskite (BEA 2 PbBr 4 where BEA is 2‐bromine ethylamine) with exceptional broadband photoluminescence (PL), which originates from multiple STE states. In particular, the unique energy‐level configuration of STEs with respect to free excitons is revealed by exploiting optical spectroscopy. Consequently, these distinct phenomena empower the broadband photodetection capability of BEA 2 PbBr 4 photodetectors over a wide range from ultraviolet to near‐infrared wavelengths. These results provide an essential understanding of the intriguing photophysics of STEs and shed new light on the future development of single‐component perovskite broadband optoelectronic devices.
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