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首页> 外文期刊>AIP Advances >Magnetic field-induced ferroelectric domain structure evolution and magnetoelectric coupling for [110]-oriented PMN-PT/Terfenol-D multiferroic composites
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Magnetic field-induced ferroelectric domain structure evolution and magnetoelectric coupling for [110]-oriented PMN-PT/Terfenol-D multiferroic composites

机译:[110]取向PMN-PT / Terfenol-D多铁复合材料的磁场诱导铁电畴结构演化和磁电耦合

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Magnetic field-induced polarization rotation and magnetoelectric coupling effects are studied for [110]-oriented (1-x)Pb(Mg1/3Nb2/3)O3-xPbTiO3/Tb0.3Dy0.7Fe2(PMN-xPT/Terfenol-D) multiferroiccomposites. Two compositions of the [110]-oriented relaxor ferroelectric single crystals, PMN-28PT and PMN-33PT, are used. In [110]-oriented PMN-28PT, domains of rhombohedral (R) and monoclinic (MB) phases coexist prior to the magnetic loadings. Upon the applied magnetic loadings, phase transition from monoclinic MB to R phase occurs. In [110]-oriented PMN-33PT, domains are initially of mixed orthorhombic (O) and MB phases, and the phase transition from O to MB phase takes place upon the external magnetic loading. Compared to PMN-28PT, the PMN-33PT single crystal exhibits much finer domain boundary structure prior to the magnetic loadings. Upon the magnetic loadings, more domain variants are induced via the phase transition in PMN-33PT than that in PMN-28PT single crystal. The finer domain band structure and more domain variants contribute to stronger piezoelectric activity. As a result, the composite of PMN-33PT/Terfenol-D manifests a stronger ME coupling than PMN-28PT/Terfenol-D composite.
机译:研究了[110]取向的(1-x)Pb(Mg1 / 3Nb2 / 3)O3-xPbTiO3 / Tb0.3Dy0.7Fe2(PMN-xPT / Terfenol-D)多铁复合材料的磁场诱导极化旋转和磁电耦合效应。 [110]取向弛豫铁电单晶的两种成分是PMN-28PT和PMN-33PT。在[110]定向的PMN-28PT中,菱形(R)和单斜晶(MB)相域共存于磁性载荷之前。在施加磁性负载后,会发生从单斜MB相到R相的相变。在[110]取向的PMN-33PT中,畴最初是正交相(O)和MB相混合,并且从O到MB相的相变是在外部磁负载下发生的。与PMN-28PT相比,PMN-33PT单晶在磁性载荷之前表现出更精细的畴边界结构。在磁性负载下,与PMN-28PT单晶相比,在PMN-33PT中通过相变感应出更多的畴变体。更好的畴带结构和更多的畴变体有助于更强的压电活性。结果,PMN-33PT / Terfenol-D的复合材料表现出比PMN-28PT / Terfenol-D的复合材料更强的ME偶联。

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