Recent progress of triplet state emission in organic-inorganic hybrid metal halides

被引：17
作者：
Dong, Yiwei [1 ,2 ]
Han, Ying [1 ,3 ]
Chen, Runan [1 ,2 ]
Lin, Yufan [1 ,2 ]
Cui, Bin-Bin [1 ,2 ]
机构：
[1] Beijing Inst Technol BIT, Adv Res Inst Multidisciplinary Sci, Beijing 100081, Peoples R China
[2] BIT, Sch Mat Sci & Engn, Beijing 100081, Peoples R China
[3] BIT, Sch Chem & Chem Engn, Beijing 100081, Peoples R China
来源：
JOURNAL OF LUMINESCENCE | 2022年 / 249卷
关键词：
Room -temperature phosphorescence; Low-dimensional organic-inorganic hybrid; metal halides; Triplet state emission; Self-trapped excitons; Fluorescence; WHITE-LIGHT EMISSION; ROOM-TEMPERATURE PHOSPHORESCENCE; PEROVSKITES; EXCITONS;
D O I：
10.1016/j.jlumin.2022.119013
中图分类号：
O43 [光学];
学科分类号：
070207 ; 0803 ;
摘要：
Due to the high photoluminescence quantum yield (PLQY) and multiple-colored emissions by adjusting their composition and structures, organic-inorganic hybrid metal halides (MHs) have become promising emitters for next-generation light emitting and displays. When separate inorganic metal halides by larger organic cations in crystals, multiple low-dimensional MHs (LDMHs) at the molecular level can be constructed. These LDMHs have been widely reported to exhibit excellent photoluminescence properties which stems from radiative recombination of self-trapped excitons (STEs). Recently, efficient triplet state emission including room-temperature phosphorescence (RTP) originated from organic cations triplet states is also demonstrated in LDMHs, opening a new field for the development of phosphorescence emitters. Herein, we summarize and discuss the new progress in triplet state emission in LDMHs for a better understanding the RTP development of LDMHs for their versatile display applications.
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页数：9
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