Comparative luminescence and Judd–Ofelt analysis of Eu3+-doped Ca2GdVO6 and Sr2GdVO6 phosphors for red-emitting applications


İlhan M., Güleryüz L. F., Gökçe S., Demirer H.

MATERIALS SCIENCE & ENGINEERING B: SOLID-STATE MATERIALS FOR ADVANCED TECHNOLOGY, cilt.323, ss.118776, 2026 (SCI-Expanded)

Özet

In this study, Eu3+-activated Ca2Gd1􀀀 xVO6 and Sr2Gd1􀀀 xVO6 (x = 0–30 mol%) red-emitting phosphors were

synthesized via a conventional solid-state reaction route and systematically characterized to assess the effect of

A-site variation on their structural and photoluminescence properties. X-ray diffraction results confirmed the

single phase formation of monoclinic-Ca2GdVO6 (P21/n) and monoclinic-Sr2GdVO6 (P2/m) structures, as further

corroborated by full Rietveld refinements that yielded low-residual fits and reliable lattice parameters. SEM

micrographs revealed similar grain morphologies with marginal differences in average grain sizes. Photoluminescence

excitation spectra exhibited a broad charge transfer band (CTB) centered near 256 nm, attributed

to O2􀀀 → Eu3+ transitions, along with sharp f–f transitions and characteristic Gd3+ absorptions. Emission spectra

under blue excitation (λex = 467 nm) demonstrated dominant 5D0 → 7F2 electric dipole transitions, with higher

asymmetry ratios observed in the Ca-based system, indicating a more distorted local environment. Judd–Ofelt

(JO) analysis further confirmed this distinction through elevated Ω2 parameters, particularly at low doping

levels. The quantum efficiencies (ηQE) calculated using the Judd–Ofelt formalism were 99.56 % and 78.05 % for

the most luminescent Ca-based and Sr-based samples, respectively, while the experimentally measured IQE/EQE

values were 79.82 %/41.69 % (Ca-based) and 65.58 %/36.66 % (Sr-based). Additionally, colorimetric evaluation

revealed that both phosphor systems emitted warm reddish light with high color purity (up to ~85 % for Cabased

and ~96 % for Sr-based) and low correlated color temperature (CCT ~ 1600–2500 K), suitable for

warm-white LED and display applications. These findings highlight the tunable nature of Eu3+-activated vanadate

perovskites via A-site engineering, enabling their use in solid-state lighting, displays, and optical security.