Photoswitchable WO<sub>3−<i>x</i></sub> QD/Cu NC composite films for efficient UV detection and dual-mode anticounterfeiting
Photoswitchable fluorescent materials (PFMs) have attracted considerable attention owing to their intrinsic advantages of non-contact operation, cleanliness, and non-invasiveness. Conventional PFMs always require complicated preparation processes with poor fluorescence switching properties, which are affected by the Föster resonance energy transfer (FRET) or photoinduced electron transfer (PET) mechanism. Herein, WO<sub>3-<i>x</i></sub> QD/Cu NC composite films were prepared on different substrates <i>via</i> a solution casting method and display outstanding fluorescence switching properties owing to the super photochromic performance of WO<sub>3-<i>x</i></sub> QDs and aggregation-induced fluorescence of Cu NCs. The composite film exhibits reversible on/off switchable fluorescence under UV light irradiation and heat treatment based on the inner filter effect (IFE) mechanism. The composite film shows dynamic variations in dual-mode signals, and the applications of UV sensing and anti-counterfeiting are analyzed. Sensitive dual-mode detection is achieved in UV sensing, particularly for UVB. The composite film exhibits a dual-modal imaging capability with good reproducibility and high resolution for security information encryption and anti-counterfeiting. This work provides a novel strategy for fabricating advanced PFMs for multiple optical applications.
Authors
- Hualei Cheng
- Hongxi Gu (ORCID: https://orcid.org/0000-0003-4848-8204)
- Juan Du (ORCID: https://orcid.org/0000-0002-2990-5343)
- Dengwei Hu (ORCID: https://orcid.org/0000-0001-7961-7115)
- Jia Li (ORCID: https://orcid.org/0000-0002-5433-1521)
- Lijun Ren
- Qingshan Mu
Institutions
- Baoji University of Arts and Sciences (CN)
Publication Details
- Journal
- Dalton Transactions
- Published
- 2025-01-01
- DOI
- https://doi.org/10.1039/d5dt00440c
- Primary Topic
- Photochromic and Fluorescence Chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.00