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作 者:陈小博[1] 刘应亮[1] 谭宁会[1] 肖琴[1] 肖丽媛[1]
出 处:《稀土》2010年第3期1-5,共5页Chinese Rare Earths
基 金:国家自然科学基金(50872045;20671042);广东省自然科学基金(7005918;05200555;2006B14801003)
摘 要:采用微波辐射法合成了Sr2MgSi2O7∶Eu2+,Dy3+粉末,研究了微波辐射功率和加热时间对制备Sr2Mg-Si2O7∶Eu2+,Dy3+的影响,确定了微波法合成Sr2MgSi2O7∶Eu2+,Dy3+的最佳条件,并用x射线衍射(XRD)、荧光光谱等测试手段对其进行了表征。XRD结果表明,合成的Sr2MgSi2O7∶Eu2+,Dy3+属于四方晶系。荧光光谱测试表明,用lem=467nm作为监控波长,在200nm^450nm之间有宽的激发光谱,峰值位于398nm。用lex=398nm激发样品,其发射光谱为一宽带,峰值位于467nm。Sr2MgSi2O7∶Eu2+,Dy3+的荧光强度和余辉性能随辐射功率和时间的不同而发生变化,其中以辐射功率720W,反应时间25min时荧光强度最强,余辉时间可达8h。The blue emission Sr2 MgSi2 O7: Eu^2+ , Dy^3+ phosphor powders were prepared using a hybrid microwave synthesis. The influence of different microwave radiation power and heating time on Sr2 MgSi2 07: Eu^2 + , Dy^3+ was discussed and the optimum condition to achieve superior Sr2 MgSi2 O7: Eu^2+ , Dy^3+ phosphor is confirmed. The powders were characterized by X - ray diffraction (XRD) and photoluminescence spectra. The results show that the Sr2MgSi2O7: Eu^2+ , Dy^3+ bulk powders exhibited a tetragonal crystal structure. The excitation spectrum (λem = 467nm ) and emission spectrum (λex = 398nm ) of Sr2 MgSi2 O7: Eu^2+ , Dy^3+ are broad band spectra, and the main excitation peaking at 398nm. The main emission peaking at 467nm is ascribed to the 4f- 5d transition of Eu^2+. The emission intensity and afterglow property of Sr2 MgSi2O7: Eu^2+ , Dy^3+ phosphor change with different power and time ,and the strongest emission intensity is at 720W for 25min. The duration time lasted over 8 h.
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