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作 者:杨志平[1] 韩月[1] 宋延春[1] 赵青[1] 周东站[1] 刘玉峰[1]
机构地区:[1]河北大学物理科学与技术学院,河北保定071002
出 处:《硅酸盐学报》2012年第3期469-472,共4页Journal of The Chinese Ceramic Society
基 金:河北省自然科学基金(F2009000217)资助项目
摘 要:采用高温固相法合成了Ba2–xB2O5:xSm3+红色荧光粉。研究了Sm3+掺杂量对样品发光性质的影响。结果表明,合成物质为纯相Ba2B2O5晶体结构。主激发峰为342nm(6H5/2→4H9/2)、359 nm(6H5/2→4D3/2)、372 nm(6H5/2→6P7/2)、400 nm(6H5/2→4F7/2)、436 nm(6H5/2→4G9/2)、450~510 nm(6H5/2→4I13/2,4I9/2,4I11/2,4G7/2)。主发射为550~575 nm(4G5/2→6H5/2)、580~620 nm(4G5/2→6H7/2)及630~660 nm(4G5/2→6H9/2),其中以400 nm激发的峰值最大。随着Sm3+掺量x的增大,发光强度先增大后减小,在x=0.06时达到最大值。分析表明其浓度猝灭的机理是电偶极–电四极相互作用。The Ba2–xB2O5:xSm3+ phosphors were synthesized via the high temperature solid state reactions.The effect of the doping quantity of Sm3+ activator on the luminescence properties was investigated.The results indicate that the sample synthesized is a pure phase of Ba2B2O5.The main excitation peaks were located at 342 nm(6H5/2→4H9/2),359 nm(6H5/2→4D3/2),372 nm(6H5/2→6P7/2),400 nm(6H5/2→4F7/2),436 nm(6H5/2→4G9/2) and 450~510 nm(6H5/2→4I13/2,4I9/2,4I11/2,4G7/2),respectively.The main emission was located at 550–575 nm(4G5/2→6H5/2),580–620 nm(4G5/2→6H7/2) and 630~660 nm(4G5/2→6H9/2).The most intense emission was excited at a wavelength of 400 nm.It was found that the luminescent intensity firstly increased and then decreased with increasing Sm3+ content(x).The luminescent intensity had the best value when Sm3+ content x was 0.06.The concentration quenching mecha-nism was the electric dipole–electric quadrupole interaction in the phosphor.
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