Vu Thi Kim Lien, Le Thi Phuong, Vu Van Thu, Nguyen Dac Dien, Le Thi Oanh, Do Thi Lan Chi, Pham Thi Lien, Chu Anh Tuan, Pham Van Tuan, Hoang Gia Chuc, Manh Trung Tran, Le Tien Ha
In this study, Eu3+-doped SrY2O4 red-emitting phosphors were successfully synthesized via a conventional solid-state reaction route, and their structural, optical and luminescence properties were systematically investigated. X-ray diffraction analysis confirmed the formation of a single-phase orthorhombic SrY2O4 host, while microscopic and spectroscopic studies revealed high crystallinity and homogeneous incorporation of Eu3+ ions into the lattice. Increasing the Eu3+ concentration from 1 to 6 mol% induced a slight lattice expansion and reduced the optical band gap from 6.13 to 5.30 eV. Under near-ultraviolet and blue-light excitation, the phosphors exhibited intense red emission dominated by the 5D0 → 7FJ transition of Eu3+ ions, indicating the occupation of non-centrosymmetric lattice sites. Judd-Ofelt analysis was employed to evaluate the local environment and radiative emission properties of Eu3+ ions; the results indicate that Eu3+ ions occupy non-centrosymmetric sites with local asymmetry at C s sites, with the Ω 2 value increasing slightly from 2.623 × 10-20 to 2.795 × 10-20 cm2 as the Eu concentration rises from 1% to 5%. The optimum emission intensity was achieved at 5 mol% Eu3+, beyond which concentration quenching occurred through non-radiative energy transfer between neighboring activator ions. The phosphors demonstrated excellent thermal stability with an average activation energy of 0.242 eV, high color purity exceeding 85%, and an internal quantum efficiency of 67.74%. These results highlight the potential of SrY2O4:Eu3+ phosphors as efficient red-emitting components for warm white light-emitting diode (WLED) technologies.