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作 者:应跃芳[1] 罗孟飞[1] 王月娟[1] 谢冠群[1] 王雪琴[1] 何迈[1] 王雪俐[1]
机构地区:[1]浙江师范大学物理化学研究所浙江省固体表面反应化学重点实验室,金华321004
出 处:《高等学校化学学报》2007年第2期325-329,共5页Chemical Journal of Chinese Universities
基 金:国家自然科学基金(批准号:20473075)资助
摘 要:用改进的柠檬酸溶胶-凝胶法制备了纳米PrOr-ZrO2固溶体.采用XRD,Raman和TEM等技术对纳米PrOy-ZrO2进行了表征.结果表明,改进的柠檬酸溶胶-凝胶法制备的PrOy-ZrO2固溶体于650℃焙烧后晶粒大小在5—10nm之间;于950℃焙烧(Pr〉16%)后晶粒大小在20nm左右.Pr能有效地使ZrO2稳定在四方或立方晶相.随Pr含量的增加,PrOr-ZrO2固溶体的物相结构从单斜相逐步向四方和立方相转变.XRD和Raman得到的物相结构的差别表明,PrOy-ZrO2固溶体表层和体相结构存在不一致性,随Pr含量增加,体相逐步按照m→t→c的物相转变,表层按照m→t→t^n的物相转变.表层更易生成低对称性和无序结构.The characterization for PrOy-ZrO2 solid solutions prepared by improved sol-gel method was performed by means of Raman, XRD, TEM and so on. It is found that the grain size of PrOy-ZrO2 solid solution calcined at 650 ℃ is 5-10 nm, and that of PrOy-ZrO2 solid solution calcined at 950 ℃ [x(Pr) 〉 16% ] is about 20 nm. At a higher Pr content, phase transformation towords a higher-symmetrical phase ( tetragonal or cubic) was observed. The results of phase analysis obtained by Raman spectroscopy were different from the corresponding results of XRD, which implies a structure difference between the surface and the bulk shell of the samples. With the increase of the Pr content, the m→t→w phase tramsformation occurred in the bulk area and the m→t→t'' phase tramsformation occurred in the surface area. The surface region is more easily to form a low symmetry and disorder structure.
关 键 词:PrO-ZrO2复合氧化物 Uamsn光谱 X射线粉末衍射 溶胶-凝胶法
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