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作 者:娄长影 朱君秋[2] 邵艳群[1] 马晓磊[1] 唐电[1]
机构地区:[1]福州大学材料科学与工程学院,福建福州350108 [2]厦门理工学院材料科学与工程学院,福建厦门361024
出 处:《中国稀土学报》2014年第2期205-212,共8页Journal of the Chinese Society of Rare Earths
基 金:国家自然科学基金项目(11374053)资助
摘 要:采用热分解法制备了钛基IrO2-CeO2二元氧化物涂层电极(Ti/IrO2-CeO2)。通过X射线荧光衍射(XRD),(SEM),循环伏安和交流阻抗等方法研究了退火温度对Ti/IrO2-CeO2涂层电极组织结构与电容性能的影响。结果表明,随退火温度升高,IrO2-CeO2涂层由非晶态向晶态转变,晶化程度逐渐升高;在460~480℃高温退火,IrO2-CeO2涂层中仍含有约28%的非晶态组织,说明CeO2有抑制IrO2晶化的作用。当退火温度为380℃时,电极的晶化程度约为25%,比电容达到最大值,并具有良好的循环稳定性。电极的电荷转移电阻取决于电极的晶化程度,随退火温度升高呈阶梯下降趋势。Ti/IrO2-CeO2 electrodes were prepared by thermal decomposition at various annealing temperatures. The influence of the annealing temperature on microstructure, morphology, and capacitive performance of the Ti/IrO2- CeO2 electrodes was investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM), cyclic voltammetry and electrochemical impedance spectroscopy. The annealing temperature was found to play a significant role in affecting the microstructure and capacitive performance. The amorphous structure transformed to crystalline with increasing annealing temperature. The structure with about 28% amorphous could be still existed at 460-480℃, which indicated that CeO2 could inhibit crystallization of the IrO2. The Ti/IrO2-CeO2 electrodes annealed at 380 ℃ had the maximum specific capacitance combining with excellent cycling behavior, and the crystallization degree of the Ti/IrO2-CeO2 electrodes was about 25%. Charge transfer resistance of the electrode depended on the degree of crystallization of the electrodes, showing a ladder fall with increasing annealing temperature.
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