光致发光
材料科学
荧光
激子
光化学
肉眼
发色团
光电子学
纳米技术
化学
光学
量子力学
物理
作者
Yanni Jie,Dong Wang,Runfeng Chen,Jingyu Zhang,Wenqi Li,Jianfeng Huang,Penggao Dai,Yang Gao,Fuchun Li,Jiawen Fang
出处
期刊:Nanoscale
[The Royal Society of Chemistry]
日期:2023-01-01
卷期号:15 (7): 3337-3344
被引量:22
摘要
Carbon dots (CDs) with deep-blue thermally activated delayed fluorescence (TADF) of more than 2 s were developed, exhibiting the longest lifetime to date. In contrast to the established deep-blue TADF systems, this developed CD-based system (BNCDs) could be facilely and effectively synthesized, and more impressively, the emission lasted for more than 16 s (to the naked eye). XRD, TEM, FT-IR, and XPS analyses were conducted, and structural characterizations indicated that the CDs formed hydrogen bonding with B2O3. The temperature-dependent photoluminescence (PL) spectra demonstrated the existence of thermally activated delayed fluorescence in the composite. Further studies revealed that the B2O3 matrix restricted the vibration and rotation of CD chromophores and suppressed the non-radiative recombination of triplet excitons. Last but not least, potential applications in bioimaging, anti-counterfeiting, and information encryption were also explored. This work can provide new insights for developing metal-free and ultralong lifetime afterglow materials.
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