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Updated: Feb 20, 2026

Scale-up Chemical Synthesis of Thermally-activated Delayed Fluorescence Emitters Based on the Dibenzothiophene-S,S-Dioxide Core
Published on: October 24, 2017
Cristales individuales de bromuro de indio orgánico-inorgánico isómeros con emisión retardada y bicolor
Haichao Zhou1, Kiyonori Takahashi1,2, Takuya Okamoto1,2
1Graduate School of Environmental Science, Hokkaido University, Kita 10, Nishi 5, Sapporo, Hokkaido 060-0810, Japan. biju@es.hokudai.ac.jp.
Abstract:
Hybrid metal halides attract significant attention in materials science, chemistry, and photonics due to their attractive structural, electronic, and optical properties. However, zero-dimensional (0D) hybrid indium halides are still in their infancy. We report the first isomeric 0D indium halide single crystals showing green and delayed yellow emissions. Single-crystal X-ray structures reveal that these emissions originate from crystals with the molecular formula (C10H22N2)4In4Br20, consisting of organic ligands, InBr6 octahedra, and InBr4 tetrahedra. While both crystals carry eight corner-sharing and two face-sharing InBr6 octahedra, the four face-sharing InBr4 tetrahedra in the green-emitting isomer and two inner InBr4 tetrahedra in the yellow-emitting isomer mark the crystal isomerism, leading to distinct optical properties. The green-emitting crystals exhibit short excitonic lifetimes, whereas the radiative recombination in the yellow-emitting crystals is delayed by several hundred nanoseconds and redshifted, indicating a self-trapped exciton behaviour with a large Huang-Rhys factor and high activation energy. The structural and optical properties of the isomeric single crystals offer insights into the importance of developing 0D metal halides with multi-colour and delayed emission for sensors, LEDs, and displays.
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