Zhu Wenping, Wang Like, Yang Weijie, Chen Yahong, Liu Zengchen, Li Yanxia, Xue Yingying
College of Chemistry and Chemical Eningeering, Henan Key Laboratory of Rare Earth Functional Materials, International Joint Research Laboratory for Biomedical Nanomaterials of Henan, Zhoukou Normal University, 466001, Zhoukou, P. R. China.
J Fluoresc. 2024 Nov;34(6):2601-2612. doi: 10.1007/s10895-023-03462-2. Epub 2023 Oct 20.
Owing to the ultralong afterglow, room temperature decay phosphorescence nanomaterials have aroused enough attention. In the work, by simple one-pot solid-state thermal decomposition reaction, aggregate carbon dots (CDs) was prepared from trimesic and boric acid. Based on the intermolecular hydrogen bonds and intramolecular π-π stacking weak interaction from precursors, CDs was encapsulated in boron oxide matrix and formed aggregation. The aggregate state of CDs facilitated the triplet excited states (Tn), which could induce the room temperature decay phosphorescence properties. By careful investigation, under different excitation wavelengths at 254 and 365 nm, the aggregate CDs showed > 15 s and > 3 s room temperature phosphorescence emission in the naked eye, which was associated with 1516.12 ms and 718.62 ms lifetime respectively. And the aggregate CDs exhibited widespread application in encoding encryption, optical anti-counterfeiting and fingerprint identification etc. The interesting aggregate CDs revealed unexpected ultralong-afterglow room temperature decay phosphorescence properties and the work opened a window for constructing ultralong-afterglow room temperature decay phosphorescence aggregate CDs nanomaterials.
由于超长余辉,室温磷光纳米材料引起了足够的关注。在这项工作中,通过简单的一锅固态热分解反应,由均苯三甲酸和硼酸制备了聚集态碳点(CDs)。基于前驱体分子间的氢键和分子内π-π堆积弱相互作用,CDs被包裹在氧化硼基质中并形成聚集体。CDs的聚集态促进了三重激发态(Tn),从而诱导出室温磷光特性。经过仔细研究,在254和365nm的不同激发波长下,聚集态CDs在肉眼下显示出大于15秒和大于3秒的室温磷光发射,其寿命分别为1516.12毫秒和718.62毫秒。并且聚集态CDs在编码加密、光学防伪和指纹识别等方面展现出广泛应用。有趣的聚集态CDs展现出意想不到的超长余辉室温磷光特性,这项工作为构建超长余辉室温磷光聚集态CDs纳米材料打开了一扇窗口。