Deep-blue thermally activated delayed fluorescence carbon dots with ultralong lifetime

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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Nanoscale 2023-02, Vol.15 (7), p.3337-3344
Hauptverfasser: Jie, Yanni, Wang, Dong, Chen, Runfeng, Zhang, Jingyu, Li, Wenqi, Huang, Jianfeng, Dai, Penggao, Gao, Yang, Li, Fuchun, Fang, Jiawen
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung: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 B 2 O 3 . The temperature-dependent photoluminescence (PL) spectra demonstrated the existence of thermally activated delayed fluorescence in the composite. Further studies revealed that the B 2 O 3 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. Deep blue thermally activated delayed fluorescence of carbon dots with lifetime up to 2.02 s, which the longest, has been achieved.
ISSN:2040-3364
2040-3372
DOI:10.1039/d2nr05104d