化学
八面体
溴化物
铟
橙色(颜色)
结晶学
光化学
晶体结构
无机化学
有机化学
食品科学
作者
Niu Sun,Jiawei Lin,Shihui He,Jindong Cao,Zhongnan Guo,Jing Zhao,Quanlin Liu,Wenxia Yuan
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2023-02-08
卷期号:62 (7): 3018-3025
被引量:19
标识
DOI:10.1021/acs.inorgchem.2c03653
摘要
Zero-dimensional (0D) In-based organic-inorganic metal halides (OIMHs) have received growing interest in recent years as promising luminescent materials. However, the high efficiencies of 0D In-based OIMHs are all dependent on Sb doping in the existing literature. Here, we report a novel 0D In-based OIMH (C10H22N2)2In2Br10, which exhibits intrinsic broadband emission (610 nm), and the photoluminescence quantum yield (PLQY) can reach 70% without Sb doping. (C10H22N2)2In2Br10 shows a typical 0D structure with three different In-Br polyhedra (two octahedra and one tetrahedron) separated by large organic cations. Based on the optical property measurements and theoretical calculations, we demonstrate that (C10H22N2)2In2Br10 is an indirect semiconductor with a band gap of 3.74 eV, and the In-Br inorganic moiety is primarily responsible for the intense emission of (C10H22N2)2In2Br10. Interestingly, the unique double octahedral configuration in (C10H22N2)2In2Br10 may enhance the structural distortion and stimulate the self-trapped excitons (STEs), leading to the related high PLQY. Our work provides a novel 0D In-based OIMH with high-efficiency intrinsic emission, which is helpful for understanding the structure-PL relationships of hybrid halides.
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