Green emitting long afterglow phosphor SrAl₂O₄: Eu²⁺, Dy³⁺ was synthesized via the combustion method. The physical phase analysis was carried out by X-ray diffraction, the results show that the introduction of Eu²⁺ into the lattice of the matrix resulted in a broad green emission centered at 508 nm, which is ascribed to the characteristic 4f⁶5d¹ to 4f⁷ electronic dipole allowed transition of Eu²⁺ ions. The doping of Eu²⁺ and Dy³⁺ did not change the physical phase of the crystals. Dy³⁺, as a coactivator, does not emit light itself, but can generate holes to form a trap energy level, which acts as an electron trap center to capture some of the electrons generated by the excitation of Eu²⁺. After excitation has ceased, let them gradually to transfer to the ground state for long afterglow luminescence. Then, we investigate the optical characterizations of different samples excited by X-ray. We found that SrAl₂O₄: Eu²⁺, 0.5% Dy³⁺ has this higher luminous intensity and afterglow. Its fluorescence lifetime is about 720 ns, and its quantum yield can reach 15.18%. Through search engine marketing (SEM) and energy dispersive X-ray spectroscopy (EDX), it has been proved that the sample has been successfully synthesized and its component content has been confirmed. The Eg value calculated from the diffuse reflectance spectrum is 4.61eV. The prepared SrAl₂O₄: Eu²⁺, Dy³⁺ luminescent powder is combined with Polydimethylsiloxane substrate for anticounterfeiting application, which provides a novel idea and method for the development of the anticounterfeiting field.

A series of long-afterglow luminescent materials (SrAl₂O₄: Eu²⁺ (SAOE), SrAl₂O₄: Eu²⁺, Dy³⁺ (SAOED) and SrAl₂O₄: Eu²⁺, Dy³⁺, Gd³⁺ (SAOEDG)) was synthesized via the combustion method. Temperature and concentration control experiments were conducted on these materials to determine the optimal reaction temperature and ion doping concentration for each sample. The crystal structure and luminescent properties were analyzed via X-ray diffraction (XRD), photoluminescence (PL), and afterglow attenuation curves. The outcomes demonstrate that the kind of crystal structure and the location of the emission peak were unaffected by the addition of ions. The addition of Eu²⁺ to the matrix’s lattice caused a broad green emission with a central wavelength of 508 nm, which was attributed to the characteristic 4f⁶5d¹ to 4f⁷ electronic dipole, which allowed the transition of Eu²⁺ ions. While acting as sensitizers, Dy³⁺ and Gd³⁺ could produce holes to create a trap energy level, which served as an electron trap center to catch some of the electrons produced by the excitation of Eu²⁺ but did not itself emit light. After excitation ceased, this allowed them to gently transition to the ground state to produce long-afterglow luminescence. It was observed that with the addition of sensitizer ions, the luminous intensity of the sample increased, and the afterglow duration lengthened. The elemental structure and valence states of the doped ions were determined with an X-ray photoelectron spectrometer (XPS). Scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDX) were used to characterize the samples. The results show that the sample was synthesized successfully, and the type and content of ions in the fluorescent powder could be determined. The fluorescence lifetime, quantum yield, bandgap value, afterglow decay time, and coordinate position in the coherent infrared energy (CIE) diagram of the three best sample groups were then analyzed and compared. Combining the prepared phosphor with ink provides a new idea and method for the field of anti-counterfeiting through screen printing.

Herein, a series of novel long afterglow nanophosphors BaYAl₃O₇:Eu²⁺, Nd³⁺ was synthesized by the combustion method. The investigation encompassed the characterization of X-ray diffraction, morphology, chemical valence, elemental composition, and photoluminescence behavior of BaYAl₃O₇:Eu²+ and BaYAl₃O₇:Eu²⁺, Nd³⁺ nanoparticles. Under 365 nm excitation, BaYAl₃O₇:Eu²⁺ and BaYAl₃O₇:Eu²⁺, Nd³⁺ show emission bands centered at 497 nm and 492 nm, which are attributed to the 4f⁶5d→4f⁷ transition of Eu²⁺ ions. The optimal samples of BaYAl₃O₇:0.03Eu²⁺ and BaYAl₃O₇:0.03Eu²⁺, 0.02Nd³⁺ have average fluorescence lifetimes of 850 ns and 1149 ns, respectively. The co-doping of Nd³+ ions as the trap centers produced long afterglow luminescence properties, and the afterglow time could reach up to 8 min. Furthermore, the fluorescent powder can be mixed with polyacrylic acid to prepare anti-counterfeiting inks; a clover pattern and snowflake pattern have been successfully printed using screen printing technology, proving its potential application in the field of anti-counterfeiting.

Herein, a series of Ba_0.5Sr_0.5Al₂O₄: xEu²⁺ (x = 0.01, 0.02, 0.03, 0.04, 0.06) nanophosphors were synthesized by a combustion method. The investigation encompassed the characterization of the phase purity, morphology, elemental composition, and photoluminescence behavior of Ba_0.5Sr_0.5Al₂O₄: xEu²⁺ nanoparticles. Under excitation by 303 nm and 365 nm ultraviolet light, the nanoparticles exhibited blue-green emission arising from the 4f⁶5d→4f⁷ transition of Eu²⁺ ions. The optimal doping concentration was determined to be 2%. Notably, the nanoparticles demonstrated fluorescence lifetimes and quantum yields of 1010 ns ($\lambda$_ex = 303 nm), 112 ns ($\lambda$_ex = 365 nm), 10.5%, and 10.3%, respectively. Additionally, a comprehensive analysis of the band structure and electronic density of states was conducted, revealing a theoretical direct band gap of 4.05 eV for the Ba_0.5Sr_0.5Al₂O₄ host. In addition, the prepared fluorescent powder can be used to prepare fluorescent flexible films. This film does not change the characteristic emission of Eu²⁺ ions and has more stable physicochemical properties, which may be more suitable for use in harsh environments. Also, the fluorescent powder can be blended with polyacrylic acid to form colorless anti-counterfeiting ink that can be applied to banknotes as an anti-counterfeiting mark. A clover pattern was successfully printed using screen-printing technology, proving its potential application in the field of anti-counterfeiting.