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首页> 外文期刊>Applied Surface Science >Very high temperature stability and excellent dielectric properties of a novel X9R-type Ca_(1-x)Sr_xCu_3Ti_4O_(12)/TiO_2 nanocomposite synthesized by a polymer pyrolysis technique
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Very high temperature stability and excellent dielectric properties of a novel X9R-type Ca_(1-x)Sr_xCu_3Ti_4O_(12)/TiO_2 nanocomposite synthesized by a polymer pyrolysis technique

机译:通过聚合物热解技术合成的新型X9R型Ca_(1-x)Sr_xcu_3Ti_4O_(12)/ TiO_2纳米复合材料非常高的温度稳定性和优异的介电性能

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摘要

A polymer pyrolysis solution method was employed for the synthesis of Ca1-xSrxCu3Ti4O12/TiO2 ceramics. At 30 degrees C and 1 kHz, a high dielectric constant (epsilon') similar to 4193-10,110 and very low loss tangent (tan delta) similar to 0.009-0.039 were achieved. Interestingly, a Ca0.95Sr0.05Cu3Ti4O12/TiO2 ceramic sintered at 1060 degrees C for 5 h displayed a di-electric temperature coefficient (Delta epsilon') of less than +/- 15% over a temperature range -60-210 degrees C, which is wider than that ever reported. All ceramic samples displayed nonlinear J-E characteristics. Sr2+ doping significantly enhanced the breakdown field (E-b) and the nonlinear coefficient (alpha) with the highest E-b of similar to 20,548 V.cm(-1) and a value of similar to 52.06 in a Sr2+-doped ceramic where x=0.05. X-Ray Diffraction (XRD) and Field Emission Scanning Electron Microscopy (FESEM) were employed to study of the influence of Sr2+ doping on the microstructure and phase composition of the samples. The oxidation state of Cu ions in ceramic samples was investigated using X-Ray Absorption Near Edge Spectroscopy (XANES).
机译:用于合成Ca1-XsrxCu3Ti4O12 / TiO2陶瓷的聚合物热解溶液方法。在30摄氏度和1 kHz下,实现了类似于4193-10,110和类似于0.009-0.039的4193-10,110和非常低的损耗切线(TaN Delta)的高介电常数(epsilon')。有趣的是,在1060摄氏度下烧结5小时的Ca0.95Sr0.05cu3Ti4O12 / TiO2烧结在-60-210℃的温度范围内小于+/- 15%的二电动温度系数(Delta epsilon'),这比曾经报道的那样宽。所有陶瓷样本都显示出非线性J-E特性。 SR2 +掺杂显着增强了击穿场(E-B)和非线性系数(α),其最高的E-B类似于20,548 V.CM(-1),并且在SR2 + - 掺杂陶瓷中类似于52.06的值,其中X = 0.05。 X射线衍射(XRD)和场发射扫描电子显微镜(FESEM)用于研究Sr2 +掺杂对样品的微观结构和相组成的影响。使用X射线吸收附近边缘光谱(Xanes)研究了陶瓷样品中Cu离子的氧化状态。

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