摘要
Narrow-band red phosphors excited by blue light are vital for high-color-rendering lighting and wide-color-gamut displays. Nevertheless, the commonly utilized red phosphors exhibit considerable deficiencies in hydrothermal stability and color purity, thus constraining their practical usage. In this study, by using a developed doping strategy with Ca 2+ to regulate a local crystal field and the possible preferential occupation behavior of the Sr 2 YNbO 6 :Eu 3+ red phosphor with a double perovskite structure, it is found that their luminescence intensity and thermal stability are significantly enhanced. High-resolution scanning transmission electron microscope (STEM) measurements equipped with an aberration corrector revealed that Eu 3+ occupied the Sr 2+ or Y 3+ sites, forming two emission centers. This resulted in significant changes in the emission intensity at 594 nm and 611 nm with changes in the excitation wavelength. Furthermore, the introduction of Ca 2+ can increase the proportion of Eu 3+ at the Sr 2+ site, thereby enhancing the emission of the 5 D 0 → 7 F 2 transition at 611 nm. Meanwhile, we have significantly improved the color purity and thermal stability of the obtained red phosphors. The current findings reveal the site-selective luminescence mechanism in Eu 3+ -activated double perovskite structures and propose a cation substitution strategy to optimize excitation and emission simultaneously. This approach may provide an effective pathway for the design of high-performance red phosphors for advanced optoelectronic applications.
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