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Room-temperature ferroelectricity in strained SrTiO3

机译:应变SrTiO3中的室温铁电

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Systems with a ferroelectric to paraelectric transition in the vicinity of room temperature are useful for devices. Adjusting the ferroelectric transition temperature (T-c) is traditionally accomplished by chemical substitution - as in BaxSr1-xTiO3, the material widely investigated for microwave devices in which the dielectric constant (epsilon(r)) at GHz frequencies is tuned by applying a quasi-static electric field(1,2). Heterogeneity associated with chemical substitution in such films, however, can broaden this phase transition by hundreds of degrees(3), which is detrimental to tunability and microwave device performance. An alternative way to adjust Tc in ferroelectric films is strain(4-8). Here we show that epitaxial strain from a newly developed substrate can be harnessed to increase Tc by hundreds of degrees and produce room-temperature ferroelectricity in strontium titanate, a material that is not normally ferroelectric at any temperature. This strain-induced enhancement in T-c is the largest ever reported. Spatially resolved images of the local polarization state reveal a uniformity that far exceeds films tailored by chemical substitution. The high er at room temperature in these films ( nearly 7,000 at 10 GHz) and its sharp dependence on electric field are promising for device applications(1,2).
机译:在室温附近具有铁电至顺电转变的系统可用于设备。调节铁电转变温度(Tc)的方法通常是通过化学替代来完成的-如BaxSr1-xTiO3一样,这种材料已广泛用于微波设备,其中通过应用准静态频率来调节GHz频率下的介电常数(epsilon(r))电场(1,2)。但是,与此类薄膜中的化学取代相关的异质性可使该相变扩大数百度(3),这不利于可调性和微波器件性能。调节铁电薄膜中Tc的另一种方法是应变(4-8)。在这里,我们表明,可以利用来自新开发基板的外延应变将Tc提高数百度,并在钛酸锶中产生室温铁电,钛酸锶是一种在任何温度下通常都不是铁电的材料。这种应变诱导的T-c增强是有史以来最大的报道。局部极化状态的空间分辨图像显示出的均匀性远远超过了通过化学取代定制的薄膜。这些薄膜在室温下的较高er(在10 GHz时接近7,000)及其对电场的强烈依赖性有望用于器件应用(1,2)。

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