将硝酸钇铕和较便宜的水溶性含硫燃烧剂溶于乙醇-水溶液,通过新的乙醇辅助燃烧法合成了一次粒径约20nm的硫氧化钇(Y2O2S:Eu)发光材料。研究结果表明:采用硫代乙酰胺作为燃烧剂时,燃烧反应产物为Y2O2S:Eu及微量的Y2O3:Eu。而采用硫脲作为燃烧剂,燃烧反应产物为Y2O3:Eu,Y2O2S:Eu和/或Y2O2SO4:Eu的混合物。利用Eu^3+离子的。D0→Fi.跃迁导致的红色发光作为荧光探针,根据其在Y2O3(λem=610nm),Y2O2S(λem1=625nm,λem2=615nm),Y2O2SO4(λem1=613,λem2=615nm)基质中的光致发光光谱和X射线发光光谱位置和强度不同,来确定生成物中Y2O3:Eu,Y2O2S:Eu,Y2O2SO4:Eu物相的组成。
Y2O2S : Eu nano crystallines with primary particle size about 20nm were prepared by a modified ethanol-assisted combustion synthesis method using yttrium/europium nitrate and inexpensive sulfur-containing organic fuel in ethanol-aqueous solution. It is shown that single Y2O2S : Eu nano crystallines are obtained using thioacetamide as organic fuel,and a mixture of Y2O3 : Eu,Y2O2S : Eu and/or Y2O2SO4 : Eu are acquired using thiourea as fuel. The spectrum profile in red emission region of Eu^3+ due to the ^5 D0→7 Fi transition is adopted as a spectroscopic probe to detect the phase of Y2O3 (λem = 610nm), Y2O2S (λem1= 625nm,λem2= 615nm), and Y2O2SO4 (λem=613 and 615nm) in the as-received samples according their peak positions and relative intensities of photoluminescence and X ray luminescence emission spectra.