A one-step approach to synthesize Na 2SiF 6:Mn 4+and K 2SiF 6:Mn 4+ red phosphors by co-precipitation is reported in this paper.
A one-step approach to synthesize Na 2SiF 6:Mn 4+and K 2SiF 6:Mn 4+ red phosphors by co-precipitation is reported in this paper. The phosphors were precipitated from a silicon fluoride solution with NaF and Na 2MnO 4 (Na 2SiF 6:Mn 4+ preparation) or KF and K 2MnO 4 (K 2SiF 6:Mn 4+ preparation) using H 2O 2 to reduce Mn 7+ to Mn 4+ at room temperature. Na 2SiF 6:Mn 4+ was also prepared through a convenient two-step route with K 2MnF 6 as a raw material. The obtained Na 2SiF 6:Mn 4+ phosphors have hexagonal structures with space group D 3 2- P321 and no impurity phase when they were examined via X-ray diffraction. Photoluminescence, photoluminescence excitation, thermal luminescence, and luminescence decay time were considered to determine the optical properties of the fluoride complexes. The prepared phosphors exhibited bright red emission under 460 nm light excitation and low-thermal quenching (∼92% of the luminescent intensity at 423 K). Increasing the concentration of Mn 4+ enhanced the luminescence intensity. A warm white light LED with high color rendering index ( R a = 86 and R9 = 61) was fabricated by employing Na 2SiF 6:Mn 4+ as red phosphors and commercial Y 3Al 5O 12:Ce 3+ as yellow phosphors on a blue-InGaN chip.