The Combination of Upconversion Nanoparticles and Perovskite Quantum Dots with Temperature-Dependent Emission Colors for Dual-Mode Anti-Counterfeiting Applications

8Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.

Abstract

Novel and high-security anti-counterfeiting technology has always been the focus of attention and research. This work proposes a nanocomposite combination of upconversion nanoparticles (UCNPs) and perovskite quantum dots (PeQDs) to achieve color-adjustable dual-mode luminescence anti-counterfeiting. Firstly, a series of NaGdF4: Yb/Tm UCNPs with different sizes were synthesized, and their thermal-enhanced upconversion luminescence performances were investigated. The upconversion luminescence (UCL) intensity of the samples increases with rising temperature, and the UCL thermal enhancement factor rises as the particle size decreases. This intriguing thermal enhancement phenomenon can be attributed to the mitigation of surface luminescence quenching. Furthermore, CsPbBr3 PeQDs were well adhered to the surfaces and surroundings of the UCNPs. Leveraging energy transfer and the contrasting temperature responses of UCNPs and PeQDs, this nanocomposite was utilized as a dual-mode thermochromic anti-counterfeiting system. As the temperature increases, the color of the composite changes from green to pink under 980 nm excitation, while it displays green to non-luminescence under 365 nm excitation. This new anti-counterfeiting material, with its high security and convenience, has great potential in anti-counterfeiting applications.

Cite

CITATION STYLE

APA

Zhang, Q., Gao, Y., Cheng, L., Li, Y., Xu, S., & Chen, B. (2023). The Combination of Upconversion Nanoparticles and Perovskite Quantum Dots with Temperature-Dependent Emission Colors for Dual-Mode Anti-Counterfeiting Applications. Nanomaterials, 13(24). https://doi.org/10.3390/nano13243102

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free