Host Latties 图形.doc

Host Lattices Preparation Route Morphology and size PEP Addition BaWO4:Pr3+ Hydrothermal method Egg-shape, olive-like, quasi-sphere micro-crystals. Size: several micro-meter (m) 642nm CTAB, PVA, EDTA-2Na,citric acid CaWO4:Pr3+ Typical high-temperature solid-state method Enlarged crystal size: 20 -40m with addition of H3BO3 617nm 648nm 603nm Addition of H3BO3 as assistant flux CaMoO4:Pr3+,Pr4+, CaWO4:Pr3+, Pr4+ High-temperature solid-state method Powder phosphors, 651nm Pr3+,Pr4+ co-doping BaMoO4:Pr3+ a convenient solid-state method. A strong red emission 643 nm 3P0→3F2 transition of Pr3+ adding an alkali chloride as charge compensation reagent obviously improve emission intensity Ln1.9Pr0.1(WO4)3 (Ln= Gd or La) Sol-gel approach Powder immobilized in silica xero-gel, phosphor galsses 648nm EDTA, PEG400, TMOS Pr2(MoO4)3 Standard ceramic route Crystal 649nm Crystal structure refinement Ca9Pr(PO4)7 Solid-state reaction Powder Preheated at 400℃ for 6h 650nm Calcinated about 1150℃ K2YZr(PO4)3: Pr3+,Mn2+ Solid-state reaction Single-phase powder 631nm 980℃ for 8h in C reducing atm LaPO4:Gd3+,Pr3+ under vacuum-ultraviolet (vuv) light excitation (La0.65Gd0.35)0.95Pr0.05PO4 a filtered Hg lamp Pr3+-sensitized LaPO4:Gd3+ is a candidate of uv-B phosphors for xenon-excimer discharge vuv lamps. ZnS:Pr3+,Mn2+ Complementary blending and co-doping (solid-state) Powder KCl flux CIE coordinates (0.36,0.32) Brightness:17.9cd/m2 Tube furnace 800-1200℃ for 1h in an N2 atmosphere CaS: Pr3+ Conventional solid-state reaction Powder, activated charcoal as reducing agent Thermoluminescence glow curves analysis CaS: Pr3+ chemical co-precipitation route NaCl, KCl and NH4Cl as flux. Powder, and post-annealing process. Pseudo-spherical shape 496nm 900℃ for 1 h duration SrS:Pr3+ SrS and PrF mixed with Nacl as flux Annealing in vacuum The highest luminescence Then, by roasting the mix in a dry nitrogen atmosphere with an addition of sulfur vapor Pr concentration, the tempera