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Electric property, anti-reduction mechanism of (1-x)BaTiO_3-xBiCoO_3-Mn ceramics

机译:电特性,(1-x)BATIO_3-XBICOO_3-MN陶瓷的抗还原机制

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摘要

0.5wt%MnO_2-doped (1 - x)BaTiO_3-xBiCoO_3 ceramics short as (1 - x)BT-xBC-M sintered in air and reducing atmosphere via solid-state process were investigated. The X-ray diffraction results showed that solid solubility in (1 - x)BT-xBC ceramics sintered in the air was higher than that in reducing atmosphere. (1 - x)BT-xBC-M ceramics sintered in air transformed from tetragonal to pseudo-cubic phase when x≥0.1. The scanning electron microscopy results indicated that the average grain size increased with the BC component increasing; however, opposite phenomena occurred in samples sintered in the reducing atmosphere. The dielectric temperature curves of samples sintered in reducing atmosphere were flatted with excellent insulation resistivity of an order of magnitude of 10~(13) Ω·cm, while anomalous dielectric constant and dielectric toss of samples sintered in the air with deteriorated insulation resistivity of an order of magnitude of 10~7 Ω·cm. The anti-reduction mechanism of (1 - x)BT-xBC-M system was explained by the "electron-hole" trapping effect and formation of defect dipoles [Mn"_(Ti) - V_(oe)]and[2Co'_(Ti)- V_(oe)].
机译:研究了0.5wt%mnO_2-掺杂(1 - x)batio_3-xbicoo_3陶瓷短AS(1 - x)通过固态过程中的空气中的空气和减少气氛的BT-XBC-M。 X射线衍射结果表明,在空气中烧结的(1- X)BT-XBC陶瓷中的固体溶解度高于降低气氛。 (1 - x)当x≥0.1时从四边形转变为伪立方相的空气中的BT-XBC-M陶瓷。扫描电子显微镜结果表明,平均晶粒尺寸随着BC分量的增加而增加;然而,在还原气氛中烧结的样品中发生相反的现象。在还原气氛中烧结的样品的介电温度曲线以优异的绝缘电阻率为10〜(13)Ω·cm,而在空气中烧结的样品的异常介电常数和电介质折腾,具有劣化的绝缘电阻率幅度为10〜7Ω·cm。通过“电子 - 孔”捕获效果和缺陷偶极子[Mn“_(Ti) - V_(OE)]和[2CO'的抗还原机制解释了(1- X)BT-XBC-M系统的抗还原机制。 _(ti) - v_(oe)]。

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  • 来源
    《Journal of Materials Research》 |2021年第5期|1037-1047|共11页
  • 作者单位

    State Key Laboratory of Advanced Technology for Materials Synthesis and Processing International School of Materials Science and Engineering Wuhan University of Technology Wuhan 430070 China;

    State Key Laboratory of Advanced Technology for Materials Synthesis and Processing International School of Materials Science and Engineering Wuhan University of Technology Wuhan 430070 China Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory Xianhu Hydrogen Valley Foshan 528200 Peoples Republic of China;

    State Key Laboratory of Advanced Technology for Materials Synthesis and Processing International School of Materials Science and Engineering Wuhan University of Technology Wuhan 430070 China;

    State Key Laboratory of Advanced Technology for Materials Synthesis and Processing International School of Materials Science and Engineering Wuhan University of Technology Wuhan 430070 China;

    State Key Laboratory of Advanced Technology for Materials Synthesis and Processing International School of Materials Science and Engineering Wuhan University of Technology Wuhan 430070 China Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory Xianhu Hydrogen Valley Foshan 528200 Peoples Republic of China;

    State Key Laboratory of Advanced Technology for Materials Synthesis and Processing International School of Materials Science and Engineering Wuhan University of Technology Wuhan 430070 China;

    State Key Laboratory of Advanced Technology for Materials Synthesis and Processing International School of Materials Science and Engineering Wuhan University of Technology Wuhan 430070 China;

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