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Traditional fluorescent materials used in the anti-counterfeiting field usually exhibit monochromatic luminescence at a single-wavelength excitation, which is easily forged by sophisticated counterfeiters. In this work, Zn

The majority of the fabrication procedures of lanthanide-doped materials involve thermal treatment that often results in crystallite regrowth, stabilizing the specific crystal structure and resulting in luminescence enhancement. The efficiency and intensity of up-conversion luminescence are closely related to the structure and synthesis process of the materials. Herein, well-crystallized and pure tetragonal NaY(MoO4)2 microcrystals with a uniform octahedral shape have been successfully synthesized via an environmentally friendly hydrothermal method, followed by annealing treatment. The phases, structures, morphologies, and compositions of the synthesized products annealed at 500-1000 °C remain unchanged, indicating high thermal stability. Furthermore, the NaY(MoO4)2:Yb3+/Er3+ microcrystals exhibit strong green emission when irradiated using infrared (980 nm) or ultraviolet (378 nm) wavelengths. Upon 980 nm excitation, up to 37-fold luminescence enhancement is achieved when the samples are annealed at about 700 °C. Interestingly, the high colour purity of the strong green emission is not only independent of the dopant concentration and heat treatment temperature, but it is also independent of the excitation conditions, including power and wavelength, and this makes it particularly suitable as a green safety signal light and luminescent security ink in paintings. As-prepared safety inks with NaY(MoO4)2:Yb3+/Er3+ microcrystals were used for visual fingerprint recognition printed on A4 paper with three-level fingerprint security features, significantly increasing the difficulty of illegal imitation and enhancing the levels of anti-counterfeiting.

Hexagonal-phase NaYbF4:Er(3+) upconversion nanoparticles (UCNPs) have been synthesized via a co-precipitation method in high-boiling-point solvents, and remarkably enhanced upconversion luminescence, particularly in red emission bands (650-670 nm) in NaYbF4:Er(3+) UCNPs, has been achieved by Mn(2+) doping. The underlying reason for luminescence enhancement by Mn(2+) doping is explored by a series of controlled experiments, and a mechanism of enhancement based on the decrease of Na(+)-vacancies and organic adsorption is proposed. The Mn(2+) substitution disturbs the equilibrium of the charge and crystal lattice in the hexagonal-phase NaYbF4:Er(3+) UCNPs, which makes the Na(+)-vacancies that quenched luminescence become filled with Na(+) or Mn(2+) to offset the imbalance of the charge and electron cloud distortion. In addition, the Mn(2+) doping at the surface of UCNPs could reduce the organic adsorption on the surface of the UCNPs by an extra F(-) ion on the grain surface resulting in luminescence enhancement. Therefore, the Mn(2+)-doping approach provides a facile strategy for improvement of luminescence, which will impact on the field of bioimaging based on UCNP nanoprobes.

An innovative route to tune upconversion (UC) emission in β-NaYF(4):Yb(3+)/Tm(3+) nanorods through codoping a third rare-earth ion upon continuous wave excitation near 976 nm is reported. The dependence of UC emission on codopant concentration and environment temperature shows that tailored local environment and readjustable depopulation of excited-state ions are responsible for the tuning of UC luminescence. Codopant ions introduce a new distribution of active ions and a modified distance between Tm(3+) and Yb(3+) ions, making UC systems more sensitive to impurity ions than downconversion systems.