<![CDATA[The giant strain response mechanism in textured Mn-modified 0.925(Bi <ce:inf loc='post'>0.5</ce:inf>Na <ce:inf loc='post'>0.5</ce:inf>)TiO <ce:inf loc='post'>3</ce:inf>-0.075BaTiO <ce:inf loc='post'>3</ce:inf> relaxor ferroelectric ceramics]]>
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0.5Na 0.5)TiO 3-0.075BaTiO 3 relaxor ferroelectric ceramics]]>

机译:“:INF>)TIO 3 -0.075BATIO 3 铁电松弛器陶瓷]]>

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AbstractThis work highlights structural and domain evolution, orbital hybridization, and giant strain in the textured [(Bi1/2Na1/2)0.925Ba0.075](Ti0.998Mn0.002)O3(BNT-7.5BT-0.2%Mn) ceramics. The as-sintered textured specimens reveal a predominant tetragonalP4bm(fraction?94.4%) phase with a minor rhombohedralR3c(fraction?1.4%) phase. X-ray absorption spectra indicate reduced hybridization between the O 2pand the Na 3sp/Bi 6sp/Ti3dorbitals, implying decreased atomic bonding due to Mn doping. A mixture of Mn2+, Mn3+, and Mn4+valence states was identified in the ceramic matrix. In-situ electric (E)-field dependent XRD results show a reversibleE-field-induced phase transition, suggesting an ergodic relaxor ferroelectric. AnE-field-induced giant strain of ?0.495% at room temperature is attributed to the oriented relaxor ferroelectricP4bmphase and decreased bonding strength, which facilitate a transition from relaxor to ferroelectric phase. The poled specimen atE?=?60?kV/cm shows a structural transition sequence of tetragonalP4bm?+?rhombohedralR3c?220°CtetragonalP4bm?483°Ccubic.Highlights?AnE-field-induced giant strain mechanism in relaxor ferroelectric is proposed.?The poled specimen proposed a structural phase transition sequence during heating.?Electromechanical strain, structural transition, and atomic bond were studied.]]>
机译:<![CDATA [ 抽象 这项工作突出了纹理的结构和域演化,轨道杂交和巨大应变[(bi 1/2 NA 1/2 0.925 BA 0.075 ](TI 0.998 MN 0.002 )O 3 (BNT-7.5BT-0.2%MN)陶瓷。烧结纹理样本显示出主要的四方 p 4 bm (分数?94.4%)相阶段,核心rhombohedral R 3 C (分数?1.4%)相。 X射线吸收光谱表明O 2 p 和Na 3s之间的杂交降低,斜体> p / bi 6 sp < / ce:斜体> / ti 3d 轨道,暗示由于Mn掺杂引起的原子粘合。 Mn 2 + ,mn 3 + ,和mn 4 + 价态。原位电气( e - 字段依赖xrd结果显示可逆 e - 场诱导的相变,表明ergodic松弛器铁电。 e - 菲尔德诱导的巨大菌株在室温下0.495%归因于面向松弛剂铁电 p 4 BM 相位和降低的粘接强度,便于从松弛剂到铁电相的过渡。在 e Δ=Δ= 60?kv / cm显示四边形 p 4 bm的结构转变序列?+?rhombohedral r 3 c →< / MML:MO> 220 °C 四方 P 4 BM 483 °C 立方体。 亮点 AN e 菲尔德诱导的诱导巨型应变机制在松弛剂铁电中。 POLRED样本在加热过程中提出了结构相转换序列。 研究机电应变,结构转变和原子键。 ]]>

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