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机构地区:[1]厦门大学化学系催化教研室固体表面物理化学国家重点实验室 [2]厦门大学物理化学研究所
出 处:《催化学报》1999年第1期25-28,共4页
基 金:福建省自然科学基金
摘 要:控制合成条件以湿化学法制备了CeZrO(n(Ce)/n(Zr)=1)固溶体.XRD结果证实催化剂前体经923K焙烧后可获得立方相Ce0.5Zr0.5O2固溶体.TEM观察到固溶体颗粒大小均一(d=11nm)、分散,呈纤毛状.在氧化和还原气氛条件下分别对固溶体进行了原位拉曼光谱研究.结果表明,除450~470cm-1处出现面心立方晶格F2g拉曼活性模式对应的强拉曼谱峰外,290~320cm-1,570~620cm-1,770~790cm-1和1160~1190cm-1处分别出现弱峰或弱肩峰,各谱峰随样品处理条件改变而有不同的变化情况;固溶体的晶体结构会因氧化还原气氛以及温度等外界条件的不同发生畸变,但基本上保持为萤石构型.Ce 0.5 Zr 0.5 O 2 solid solution was prepared by wet chemical preparation method under controlled conditions. The crystal structure of the solid solution after calcination at 923 K is face centered cubic (fluorite type) verified by XRD. The solid grain is super micro powder of fiber like. Diameter of the solid solution particle is 11 nm. In situ Raman spectra of the catalyst at 323~923 K in oxygen or hydrogen atmosphere give the strong Raman peaks at 450~470 cm -1 owing to the F 2g Raman active mode characteristic of fluorite structure. The weak Raman peaks at 290~320 cm -1 , 570~620 cm -1 , 770~790 cm -1 and 1160~1190 cm -1 are also given. The Raman peaks have different changes according to the alteration of environmental conditions, such as redox atmosphere and temperature. The Raman peaks reveal that the crystal structure is deformed in the lattice by changing the external conditions, but at the same time the fluorite structure keeps unchanged.
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