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Preparation of nanosized LaCoO3 perovskite oxide using amorphous heteronuclear complex as a precursor at low temperature

机译:以非晶态杂核配合物为前驱体,低温制备纳米LaCoO3钙钛矿氧化物

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Nanosized LaCoO3 cobaltite oxide powder with perovskite structure was successfully synthesized at a relatively low calcination temperature using an amorphous heteronuclear complex, LaCo(DTPA). 6H(2)O, as a precursor. The precursor decomposed completely into cobaltite oxide above 400 degrees C according to the DTA and TGA results. XPS revealed that the decomposed species was composed of LaCoO3 cobaltite oxide after the precursor was calcined at 500 degrees C for 2 hours. XRD demonstrated that nanosized LaCoO3 crystalline powder with perovskite structure was formed after the calcination temperature increased to 600 degrees C. The grain size and the crystal size of LaCoO3 increased with the calcination temperature from 500 degrees C to 800 degrees C, and the heat-treatment time has a less obvious effect on the grain size and the crystal size. It is a useful way to synthesize nanosized perovskite oxides using an amorphous complex as a precursor. This method can be easily quantitatively controlled. (C) 2000 Kluwer Academic Publishers. [References: 16]
机译:使用非晶态杂核配合物LaCo(DTPA)在较低的煅烧温度下成功合成了具有钙钛矿结构的纳米LaCoO3氧化钴粉末。 6H(2)O,作为前体。根据DTA和TGA结果,该前体在400摄氏度以上完全分解成氧化钴。 XPS显示,在前体在500摄氏度下煅烧2小时后,分解的物质由LaCoO3氧化钴组成。 X射线衍射(XRD)表明,煅烧温度升高到600℃后,形成了钙钛矿结构的纳米LaCoO3结晶粉。煅烧温度从500℃升高到800℃,进行热处理,LaCoO3的晶粒尺寸和晶体尺寸增大。时间对晶粒尺寸和晶体尺寸的影响较小。使用无定形配合物作为前体来合成纳米尺寸的钙钛矿氧化物是一种有用的方法。这种方法可以很容易地定量控制。 (C)2000 Kluwer学术出版社。 [参考:16]

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