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Dielectric properties of 3d transition metal substituted BaTiO_3 ceramics containing the hexagonal phase formation

机译:含六方相形成的3d过渡金属取代的BaTiO_3陶瓷的介电性能

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摘要

The role of transition metals of the 3d series from V (Z = 23) to Zn (Z = 30) is investigated in modifying the crystallographic phase contents, micro-structure and the dielectric properties of BaTiO_3 ceramics containing ≤10 at% substituents. All the transition metals brought about the phase conversion to hexagonal BaTiO_3 and the hexagonality is found to depend on Ba/Ti ratio as well as the processing conditions including the sintering temperature and the post sinter annealing. The ε_r-T characteristics are modified with increasing hexagonality by way of the tremendous decrease in dielectric constant with broad and diminished ε_(max) for the mixed phase ceramics giving way to flat ε_r-T curves for totally hexagonal specimens. Doping with >1% Zn~(2+) or ≥5% Mg~(2+) also render the ceramics completely hexagonal indicating that the crystal field effects of the 3d orbital electrons are not the cause for the conversion to hexagonal phase. Electron paramagnetic resonance (EPR) spectra of Mn-doped ceramics reveal the prevalence of defect complexes involving oxygen vacancies and different valence states of Mn occupying the Ti-sites within the corner-sharing as well as face-sharing octahedra present in hexagonal BaTiO_3. EPR results also indicate defect complexes involving electron localization at Ti-sites and oxygen vacancies around the face-sharing octahedra. On annealing the ceramics in lower oxygen partial pressures at elevated temperatures leads to the reversion to corner shared (Ti~(3+)-V_O) defect complex accompanied by the conversion to cubic/tetragonal phase. The alterations in the oxygen vacancy-metal impurity defect complexes andrnthe modifications in the oxygen close packing are the cause for the prevalence of hexagonal BaTiO_3 at room temperature.
机译:研究了从V(Z = 23)到Zn(Z = 30)的3d系列过渡金属在改变取代基≤10 at%的BaTiO_3陶瓷的晶体相含量,微观结构和介电性能方面的作用。所有引起相转变为六方BaTiO_3的过渡金属,六方性都取决于Ba / Ti比以及包括烧结温度和烧结后退火在内的工艺条件。 ε_r-T特性随着六角形的增加而改变,这是由于介电常数的极大降低,混合相陶瓷的ε_(max)变宽和减小,而使整个六角形试样的ε_r-T曲线平坦。掺杂> 1%Zn〜(2+)或≥5%Mg〜(2+)也会使陶瓷完全呈六角形,这表明3d轨道电子的晶体场效应不是转变为六角形相的原因。掺杂锰的陶瓷的电子顺磁共振(EPR)光谱显示,缺陷配合物的普遍存在,氧空位和Mn的不同价态占据了六边形BaTiO_3中存在于角共享和面共享八面体中的Ti部位的Mn。 EPR结果还表明缺陷复合物涉及钛位置的电子定位和面共享八面体周围的氧空位。在高温下以较低的氧分压对陶瓷进行退火时,会导致其转变为角共享的(Ti〜(3 +)-V_O)缺陷配合物,并转化为立方/四方相。氧空位-金属杂质缺陷配合物的变化和氧的紧密堆积的改变是六方BaTiO_3在室温下盛行的原因。

著录项

  • 来源
    《Journal of materials science》 |2008年第7期|615-626|共12页
  • 作者

    S. Jayanthi; T. R. N. Kutty;

  • 作者单位

    Materials Research Centre, Indian Institute of Science,Bangalore 560 012, India;

    Materials Research Centre, Indian Institute of Science,Bangalore 560 012, India;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
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