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Crystallization and Phase-Transition Characteristics of Sol-Gel-Synthesized Zinc Titanates

机译:溶胶-凝胶合成钛酸锌的结晶和相变特性

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The synthesis of a ZnO-TiO2 nanocomposite usually results in the formation of one or more of three compounds-Zn2TiO4, Zn2Ti3O8, and ZnTiO3-along with other secondary impurity phases, such as rutile-TiO2 or ZnO. Obtaining a phase-pure composite of either of these materials is one of the challenges in materials chemistry. For example, pure ZnTiO3 cannot be synthesized under normal conditions, because the ZnTiO3 phase readily transforms to Zn2TiO4 and rutile. Zn2Ti3O8 is reported as a metastable form of ZnTiO3. The Zn2TiO4 form is usually synthesized via solid-state reaction at high temperatures (typically above 1000 °C). In the current study, the crystalline and phase-transformation behaviors of sol-gel-synthesized zinc titanates has been investigated systematically, with regard to various Zn:Ti precursor molar ratios. X-ray diffraction (XRD) has shown that, with excess titanium precursor, zinc metatitanate (ZnTiO3) is the preferred zinc titanate phase formed at temperatures of 600-900 °C, with a direct transformation of zinc metatitanate to zinc orthotitanate (Zn2TiO4) occurring at 1000 °C. However, synthesis involving titanium precursor in the presence of excess zinc precursor forms Zn2Ti3O8 with a cubic defect spinel structure at temperatures of 700-900 °C, with a direct transformation to zinc orthotitanate occurring at 1000 °C. The current study also indicated that the percentage of zinc titanate phases can be controlled by varying the initial sol~gel reaction conditions. Spectroscopic investigations have been carried out to understand the effect of precursor (Zn(CH3COO)_2·2H2O and H2C2O4) formulations on the crystallization and phase-transition behaviors of these composites. Fourier transform infrared and Raman spectroscopy have shown the presence of the oxalate form of zinc and titanium. However, neither of these techniques could reveal if the titanium oxalate chains exist separately from zinc oxalate chains or if they combine during the initial stages of preparation. Further powder XRD investigation proposed that two separate metal oxalate chains were formed during the synthesis. Previous reports indicate that the formation of Zn2TiO4 and Zn2Ti3O8 is limited by the presence of anatase and ZnTiO3 only forms in the presence of rutile. Results from the present study confirm that, in a sol-gel synthesis, the formation of various forms of zinc titanates is influenced by the zinc oxide/titanium dioxide composition.
机译:ZnO-TiO2纳米复合材料的合成通常会导致三种化合物中的一种或多种——Zn2TiO4、Zn2Ti3O8和ZnTiO3——以及其他二次杂质相,如金红石-TiO2或ZnO。获得这两种材料中任何一种的相纯复合材料是材料化学中的挑战之一。例如,纯 ZnTiO3 在正常条件下不能合成,因为 ZnTiO3 相很容易转化为 Zn2TiO4 和金红石。Zn2Ti3O8 据报道是 ZnTiO3 的亚稳态形式。Zn2TiO4 形式通常在高温(通常高于 1000 °C)下通过固相反应合成。在目前的研究中,已经系统地研究了溶胶-凝胶合成的钛酸锌的结晶和相变行为,涉及各种Zn:Ti前驱体摩尔比。X射线衍射(XRD)表明,在600-900 °C温度下,偏钛酸锌(ZnTiO3)是首选的钛酸锌相,在1000 °C下,偏钛酸锌直接转化为正钛酸锌(Zn2TiO4)。 然而,在过量锌前驱体存在下涉及钛前驱体的合成在700-900°C的温度下形成具有立方缺陷尖晶石结构的Zn2Ti3O8,在1000°C下直接转化为正钛酸锌。 目前的研究还表明,可以通过改变初始溶胶~凝胶反应条件来控制钛酸锌相的百分比。为了了解前驱体(Zn(CH3COO)_2·2H2O和H2C2O4)制剂对这些复合材料的结晶和相变行为的影响,已经进行了光谱研究。傅里叶变换红外和拉曼光谱显示存在草酸盐形式的锌和钛。然而,这两种技术都无法揭示草酸钛链是否与草酸锌链分开存在,或者它们是否在制备的初始阶段结合。进一步的粉末XRD研究表明,在合成过程中形成了两条独立的金属草酸盐链。先前的报道表明,Zn2TiO4和Zn2Ti3O8的形成受到锐钛矿矿存在的限制,而ZnTiO3仅在金红石存在下形成。本研究的结果证实,在溶胶-凝胶合成中,各种形式的钛酸锌的形成受到氧化锌/二氧化钛组成的影响。

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