The metastable garnet lattice of Gd 3 Al 5 O 12 is stabilized by doping with smaller Lu 3+ , which then allows an effective incorporation of larger Eu 3+ activators. The [(Gd 1−x Lu x ) 1−y Eu y ] 3 Al 5 O 12 (x = 0.1-0.5, y = 0.01-0.09) garnet solid solutions, calcined from their precursors synthesized via carbonate coprecipitation, exhibit strong luminescence at 591 nm (the 5 D 0 → 7 F 1 magnetic dipole transition of Eu 3+ ) upon UV excitation into the charge transfer band (CTB) at ∼239 nm, with CIE chromaticity coordinates of x = 0.620 and y = 0.380 (orange-red). The quenching concentration of Eu 3+ was estimated at ∼5 at.% (y = 0.05), and the quenching was attributed to exchange interactions. Partial replacement of Gd 3+ with Lu 3+ up to 50 at.% (x = 0.5) while keeping Eu 3+ at the optimal content of 5 at.% does not significantly alter the peak positions of the CTB and 5 D 0 → 7 F 1 emission bands but slightly weakens both bands owing to the higher electronegativity of Lu 3+ . The effects of processing temperature (1000-1500• C) and Lu/Eu contents on the intensity, quantum efficiency, lifetime and asymmetry factor of luminescence were thoroughly investigated. The [(Gd 0.7 Lu 0.3 ) 0.95 Eu 0.05 ] 3 Al 5 O 12 phosphor processed at 1500• C exhibits a high internal quantum efficiency of ∼83.2% under 239 nm excitation, which, in combination with the high theoretical density, favors its use as a new type of photoluminescent and scintillation material.