文摘
LaGaO3:Tm3+, Yb3+ powder was synthesized by a high-energy ball milling (HEB) and a conventional solid state reaction (SSR). The X-ray diffraction patterns confirmed the LaGaO3:Tm3+, Yb3+ powder phosphors to have an orthorhombic structure. The spectrum consisted of 1G4?¡ú?sup>3H6, weak 1G4?¡ú?sup>3F4, and intense 3H4?¡ú?sup>3H6 transition bands within the f12 configuration of Tm3+, together with the 2F5/2?¡ú?sup>2F7/2 transition of Yb3+. Up-converted emission of the LaGaO3:Tm3+, Yb3+ powders were observed under laser diode excitation of 975?nm. The PL intensity of the HEB-LaGaO3:Tm3+, Yb3+ powders sintered at 1300?¡ãC were higher than those of all LaGaO3:Tm3+, Yb3+ powder samples examined. The energy transition probability of HEB-LaGaO3:Tm3+, Yb3+ powders are higher than that of the SSR-LaGaO3:Tm3+, Yb3+ powders. Compared to the solid state reaction method, synthesis by high-energy ball milling is simple and provides improved crystallinity of the host.