本研究旨在探討鹼土矽酸鹽系螢光粉體的製備與餘輝特性。利用傳統高溫固態反應法製備共摻雜不同稀土元素之BaSi2O5: Eu2+, Dy3+螢光粉體。在製備BaSi2O5母體時,討論添加不同種類的助熔劑、助熔劑添加濃度的差異及不同合成溫度對BaSi2O5母體合成的影響。摻雜激活劑時,利用Eu(NO3)3?6H2O進行水溶液的摻雜方式,以及Dy2O3的摻雜,分別觀察共摻雜Eu2+及Dy3+的先後順序、在還原氣氛下的燒成溫度、摻雜Eu2+及Dy3+濃度比例等實驗參數對其餘輝性質的影響。 實驗結果顯示,助熔劑添加2 wt.% LiF並在大氣中燒成溫度為1250°C,可合成出BaSi2O5母體較純的相,並且具有良好的發光強度。放射光譜量測結果顯示,BaSi2O5: Eu3+, Dy3+螢光粉體,Eu3+為主要的發光中心,其放射峰來自5D0→7FJ(J= 0, 1, 2, 3, 4)的躍遷,呈現橘紅光放射;BaSi2O5: Eu2+, Dy3+螢光粉體,Eu2+為主要的發光中心,其放射峰來自5D0→7FJ(J= 0, 1, 2, 3, 4)的躍遷,呈現藍綠光放射。 BaSi2O5: Eu2+, Dy3+螢光粉體具有餘輝現象,其持續發光時間可達3600秒,甚至比市面上其他餘輝材料有更長的發光時間,具有好的商業應用潛力。
This study is focused on the synthesis and afterglow characteristics of alkaline silicate phosphors. Conventional high-temperature solid state reaction method is adopted to synthesize co-doping earth element BaSi2O5: Eu2+, Dy3+ phosphors. To synthesize BaSi2O5 host, we discuss the effect of different flux, flux concentrations, and firing temperature. In activator doping process Eu(NO3)3?6H2O solution and Dy2O3 for doping, Eu2+, Dy3+ doping sequential, doping atmosphere and firing temperature, doping Eu2+ and Dy3+ concentration ratios on the afterglow properties is observed. Experimental results show that adding 2 wt.% LiF flux in the atmosphere and the firing temperature is 1250°C, can be prepared with relatively pure precursor BaSi2O5, and has a good luminous intensity. Emission spectrum measurement results show, BaSi2O5: Eu3+, Dy3+ phosphors, Eu3+ as the main emission center, radiation peaks from 5D0→7FJ(J= 0, 1, 2, 3, 4) transition, showing orange light radiation; BaSi2O5: Eu2+, Dy3+ phosphors, Eu2+ as the main luminescence centers, and its emission peak from the 5D0→7FJ(J= 0, 1, 2, 3, 4)transition, blue-green emission. BaSi2O5: Eu2+, Dy3+ phosphors with afterglow characteristics, and a presistent time about 3600 s, it has potential application in market.