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In this study, Cr3+‐doped and Mn4+‐Cr3+ co‐doped double perovskite fluoride phosphors K2LiGaF6 are prepared using a simple hydrothermal method. High‐efficiency near‐infrared (NIR) emission near 762 nm is obtained under blue‐light excitation, and the co‐doping effect of Mn4+ on the NIR luminescence properties of Cr3+ is studied. Compared with the Cr3+ single‐doped phosphor, Mn4+, and Cr3+ co‐doped K2LiGaF6 exhibit a sharp increase of 129% in NIR emission, an enhancement in the internal quantum efficiency from 82.5% to 90.0%, and an enhancement in the thermal stability at 425 K from 85.0% to 90.7%. The encapsulated NIR phosphor‐converted light‐emitting diode device at 300 mA exhibits a photoelectric conversion efficiency of 15.3%. These values exceed most previously reported results. This study provides a new approach for enhancing the luminescence properties of Cr3+‐doped fluoride NIR phosphors. [ABSTRACT FROM AUTHOR]

Fluoride phosphors as red components for warm white LEDs have attracted a tremendous amount of research attention. But these phosphors are extremely sensitive to moisture, which seriously limits their practical industrial applications. To tackle this problem, unlike all the straightforward preventive strategies, a reverse strategy "Good comes from bad" was successfully developed to treat the degraded K2SiF6 : Mn4+ (D‐KSFM) phosphor in the present study, which not only completely restores the luminescence properties, but also significantly enhances the moisture resistance at the same time. After treatment with an oxalic acid solution as restoration modifier, the emission intensity of the D‐KSFM phosphor can be restored to 103.7% of the original K2SiF6 : Mn4+ red phosphor (O‐KSFM), and the moisture resistance is remarkably improved. The restored K2SiF6 : Mn4+ (R‐KSFM) maintains approximately 62.3% of its initial relative emission intensity after immersing in deionized water for 300 min, while the reference commercial K2SiF6 : Mn4+ with a protective coating (C‐KSFM) is only 33.2%. As a proof of general applicability, this strategy was also conducted to K2TiF6 : Mn4+ phosphor, which is less moisture‐stable than K2SiF6 : Mn4+. The luminescence intensity of the degraded K2TiF6 : Mn4+ (D‐KTFM) phosphor can be restored to 162.6% of original level of the K2TiF6 : Mn4+ synthesized through a cation exchange approach without any treatment (O‐KTFM). The emission intensity of the restored K2TiF6 : Mn4+ (R‐KTFM) phosphor retains 62.8% of its initial emission intensity after soaking in deionized water for 300 min. Finally, the R‐KSFM phosphors were packaged into white light‐emitting diodes with blue InGaN chips and Y3Al5O12 : Ce3+ yellow phosphors. The WLEDs display excellent color rendition with higher color rendering index, lower color temperature (WLED‐II: Ra=83.6, R9=57.3, 3743 K, ηl=199.68 lm/W; WLED‐III: Ra=90.4, R9=94.2, 2892 K, ηl=183.3 1 m/W). The above results show that the reverse strategy can be applied in those phosphor materials with poor moisture resistance to restore luminescence properties and improve moisture resistance without excessively care about the deterioration during the production, storage and transportation. [ABSTRACT FROM AUTHOR]