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Full-spectrum lighting has become the development direction for human-centric illumination. However, the reabsorption effect caused by cyan, green and yellow multiple-phosphor packaging leads to low luminous efficiency. In this work, a broadband cyan-green phosphor is proposed to replace the cyan and yellow phosphors for highly efficient and thermally robust full-spectrum WLEDs. A new family of oxyfluoride garnet phosphors Lu 2 QMg 2 Al 3 O 9 F 3 : Ce3+ (Q = Ca, Sr, Ba) has been developed by incorporating F- into the classic LuAG: Ce3+ green phosphor. The excess charge was compensated by substituting trivalent Lu3+ and Al3+ with divalent alkaline earth element. The low covalency and phonon energy of fluorine-containing system endow these serial phosphors with efficient and thermally stable blue-shifted emission. The representative Lu 2 SrMg 2 Al 3 O 9 F 3 : Ce3+ exhibits a broadband cyan-green emission peaked at 513 nm with a 105 nm FWHM. Furthermore, outstanding quantum efficiency (88.4%) and thermal stability (94.3% @ 423 K) were achieved. This oxyfluoride phosphor was packaged with red phosphor without cyan phosphor on a blue chip. The obtained WLEDs show an excellent color rendering index (R a = 96.8) with luminous efficiency (LE = 106 lm/W). This research might pave a promising avenue for the development of next-generation full-spectrum lighting. • A new family of oxyfluoride garnet cyan-green phosphors was obtained. • The F- incorporation endows the phosphors with efficient and thermally stable blue-shifted emission. • The Lu 2 SrMg 2 Al 3 O 9 F 3 : Ce3+ exhibits a 513 nm centered emission with a 105 nm FWHM. • Ra=96.8 and LE=106 lm/W were achieved by replacing the cyan and yellow phosphor. [ABSTRACT FROM AUTHOR]

Supplement illumination is indispensable in the indoor plant cultivation domain. In this research work, double perovskite Ca 2 LuNbO 6 :Mn4+ phosphors were produced. A strategy of enhancing luminescence performance by utilizing A-site cationic fluoride as a flux was proposed. The structure and morphology of Ca 2 LuNbO 6 :Mn4+ phosphor was characterized. Under the excitation of 360 nm, the emission spectra of Ca 2 LuNbO 6 :Mn4+ phosphor cover from 600 nm to 750 nm peaking at 683 nm. It benefits the red section of chlorophyll absorption band and possesses the wavelengths of 680 nm and 700 nm demanded by photosystem I (PS I) and photosystem II (PS II) to realize Emerson enhancement effect. After adding CaF 2 as flux, the emission intensity increases by 2.5 times. Due to its compatibility with the A-site cation of host, CaF 2 agent not only lower the sintering temperature but also increase the crystallite size, which result in the enhancement of luminescence. The D q /B and optical band gap of Ca 2 LuNbO 6 host is 2.32 and 3.79 eV, respectively, which show that Mn4+ ions locate in the [NbO 6 ] octahedra of strong crystal field and host has the suitable optical band gap for Mn4+ ions. With the help of CaF 2 , the thermal stability, activation energy Δ E a , internal quantum efficiency of Ca 2 LuNbO 6 :Mn4+ phosphors are promoted at 373 K from 64.8% to 70.7% of that at 273 K, from 0.33 to 0.36 eV, and from 9.1% to 23.5%. The luminescence lifetime of Ca 2 LuNbO 6 :Mn4+ is the order of a fraction of a millisecond. Finally, the as-prepared Ca 2 LuNb 0.996 O 6 :0.004Mn4+ phosphor was successfully fabricated through a 365 nm near ultraviolet (NUV) chip, which has the peak wavelengths of 683 nm and possesses 680 nm and 700 nm demanded by PS I and PS II. It is implied that Ca 2 LuNbO 6 :Mn4+ phosphor-converted light emitting diode has prospective market in the domain of supplement illumination of plant cultivation. [ABSTRACT FROM AUTHOR]

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]