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Article Abstract

Conventional Eu-activated phosphors often suffer from severe concentration quenching at high doping levels, significantly limiting their achievable brightness and efficiency. Furthermore, achieving both high color purity and strong emission intensity in the orange-red region remains challenging. In this context, we report the successful synthesis of Eu-activated BaLuBO phosphors via a multistep solid-state reaction under ambient conditions, exhibiting intense reddish-orange emission. Upon near-ultraviolet excitation at 398 nm, the phosphors exhibited dominant emission at 593 nm with a long decay time (about 4.1 ms), attributed to the magnetic dipole-allowed D → F transition of Eu ions occupying inversion-symmetric Lu lattice sites. Remarkably, concentration quenching of Eu luminescence in BaLuEuBO was completely suppressed even at 70 mol % Eu doping ( = 0.70), which can be understood from the unique one-dimensional chain-like architecture of the host lattice that restricts inter-Eu-ion energy migration to defect states. The as-synthesized BaLuEuBO composition demonstrated an internal quantum efficiency of ∼53%, coupled with superior color purity (97.5%) as evidenced by CIE coordinates of (0.605, 0.387). Furthermore, the material displayed outstanding thermal stability, retaining ∼98% of its room-temperature emission intensity at 450 K. These combined attributes position BaLuBO:Eu as a promising phosphor for next-generation warm-white LEDs.

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http://dx.doi.org/10.1021/acs.inorgchem.5c03366DOI Listing

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