| Autor: |
Dehai Liang, Saif M. H. Qaid, Xin Yang, Shuangyi Zhao, Binbin Luo, Wensi Cai, Qingkai Qian, Zhigang Zang |
| Jazyk: |
angličtina |
| Rok vydání: |
2024 |
| Předmět: |
|
| Zdroj: |
Opto-Electronic Advances, Vol 7, Iss 3, Pp 1-11 (2024) |
| Druh dokumentu: |
article |
| ISSN: |
2096-4579 |
| DOI: |
10.29026/oea.2024.230197 |
| Popis: |
The Sb3+ doping strategy has been proven to be an effective way to regulate the band gap and improve the photophysical properties of organic-inorganic hybrid metal halides (OIHMHs). However, the emission of Sb3+ ions in OIHMHs is primarily confined to the low energy region, resulting in yellow or red emissions. To date, there are few reports about green emission of Sb3+-doped OIHMHs. Here, we present a novel approach for regulating the luminescence of Sb3+ ions in 0D C10H22N6InCl7·H2O via hydrogen bond network, in which water molecules act as agents for hydrogen bonding. Sb3+-doped C10H22N6InCl7·H2O shows a broadband green emission peaking at 540 nm and a high photoluminescence quantum yield (PLQY) of 80%. It is found that the intense green emission stems from the radiative recombination of the self-trapped excitons (STEs). Upon removal of water molecules with heat, C10H22N6In1-xSbxCl7 generates yellow emission, attributed to the breaking of the hydrogen bond network and large structural distortions of excited state. Once water molecules are adsorbed by C10H22N6In1-xSbxCl7, it can subsequently emit green light. This water-induced reversible emission switching is successfully used for optical security and information encryption. Our findings expand the understanding of how the local coordination structure influences the photophysical mechanism in Sb3+-doped metal halides and provide a novel method to control the STEs emission. |
| Databáze: |
Directory of Open Access Journals |
| Externí odkaz: |
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