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作 者:吕灼菲[1] 李轶[1] 张学建[1] 王成伟[1] 曾繁明[1] 刘景和[1]
机构地区:[1]长春理工大学材料科学与工程系,长春130022
出 处:《硅酸盐学报》2008年第10期1454-1457,共4页Journal of The Chinese Ceramic Society
基 金:吉林省科技发展计划项目(D2005505)。
摘 要:以氧化铒、氧化钇、硝酸铝及柠檬酸作为起始原料,采用溶胶–凝胶燃烧法制备 50%Er3+(摩尔分数)掺杂的 Y3Al5O12(YAG)纳米粉体。通过热重–差热分析仪,X 射线衍射仪、红外光谱仪和透射电镜研究 Er3+:YAG 粉体的相变过程、结构和形貌。结果表明:烧结温度小于 900 ℃时,前驱体粉末直接转变为纯 YAG 晶相,不形成任何中间相。随着烧结温度的增加,晶粒尺寸增大。在 900 ℃烧结的粉体尺寸约为 70~150 nm,有利于制备性能优异的 Er3+:YAG 陶瓷。The sol-gel combustion method was used to synthesize 50% Er^3+ (in mole) doped Y3A15012(YAG) nanopowder, using erbium oxide, yttria, aluminum nitrate and citric acid as starting materials. The phase transformation, structure and morphology of Er^3+:YAG precursor and the calcined powder were studied by means of thermogravimetric-lifferential thermal analysis, X-ray powder diffraction, infi'ared, and transmission election microscope methods. It was found that the precursor is converted directly into pure YAG at a relatively lower temperature (below 900 ℃) without any other intermediate phase. The crystalline size grew with the increase of the heat treatment temperature. The size of powder calcined at 900 ℃ was about 70-150nm, which is favorable for good sinterability of Er^3+:YAG ceramics.
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