首页> 外文期刊>AIP Advances >A study of the temperature dependence of the local ferroelectric properties of c-axis oriented Bi6Ti3Fe2O18 Aurivillius phase thin films: Illustrating the potential of a novel lead-free perovskite material for high density memory applications
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A study of the temperature dependence of the local ferroelectric properties of c-axis oriented Bi6Ti3Fe2O18 Aurivillius phase thin films: Illustrating the potential of a novel lead-free perovskite material for high density memory applications

机译:c轴取向Bi6Ti3Fe2O18 Aurivillius相薄膜的局部铁电性能的温度依赖性研究:说明了新型无铅钙钛矿材料在高密度存储应用中的潜力

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The ability to control the growth, texture and orientation of self-nanostructured lead-free Aurivillius phase thin films can in principle, greatly improve their ferroelectric properties, since in these materials the polarization direction is dependent on crystallite orientation. Here, we report the growth of c-plane oriented Bi6Ti3Fe2O18 (B6TFO) functional oxide Aurivillius phase thin films on c-plane sapphire substrates by liquid injection chemical vapour deposition (LI-CVD). Microstructural analysis reveals that B6TFO thin films annealed at 850°C are highly crystalline, well textured (Lotgering factor of 0.962) and single phase. Typical Aurivillius plate-like morphology with an average film thickness of 110nm and roughness 24nm was observed. The potential of B6TFO for use as a material in lead-free piezoelectric and ferroelectric data storage applications was explored by investigating local electromechanical (piezoelectric) and ferroelectric properties at the nano-scale. Vertical and lateral piezoresponse force microscopy (PFM) reveals stronger in-plane polarization due to the controlled growth of the a-axis oriented grains lying in the plane of the B6TFO films. Switching spectroscopy PFM (SS-PFM) hysteresis loops obtained at higher temperatures (up to 200°C) and at room temperature reveal a clear ferroelectric signature with only minor changes in piezoresponse observed with increasing temperature. Ferroelectric domain patterns were written at 200°C using PFM lithography. Hysteresis loops generated inside the poled regions at room and higher temperatures show a significant increase in piezoresponse due to alignment of the c-axis polarization components under the external electric field. No observable change in written domain patterns was observed after 20hrs of PFM scanning at 200°C, confirming that B6TFO retains polarization over this finite period of time. These studies demonstrate the potential of B6TFO thin films for use in piezoelectric applications at elevated temperatures and for use in non-volatile ferroelectric memory applications.
机译:原则上,控制自纳米结构无铅Aurivillius相薄膜的生长,织构和取向的能力可以极大地改善其铁电性能,因为在这些材料中,极化方向取决于微晶取向。在这里,我们报告通过液体注入化学气相沉积(LI-CVD)在c面蓝宝石衬底上生长c面取向的Bi6Ti3Fe2O18(B6TFO)功能氧化物Aurivillius相薄膜。显微组织分析表明,在850°C退火的B6TFO薄膜具有很高的结晶度,良好的织构化(Lotgering系数为0.962)和单相。观察到典型的Auririvillius板状形态,平均膜厚为110nm,粗糙度为24nm。通过研究纳米尺度的局部机电(压电)和铁电性能,探索了B6TFO在无铅压电和铁电数据存储应用中用作材料的潜力。垂直和横向压电响应力显微镜(PFM)显示出较强的面内极化,这是由于位于B6TFO薄膜平面内的a轴取向晶粒的受控生长所致。在较高温度(最高200°C)和室温下获得的开关光谱PFM(SS-PFM)磁滞回线显示出清晰的铁电特征,随着温度的升高,压电响应只有很小的变化。使用PFM光刻在200°C上写入铁电畴图案。在室温和较高温度下,极化区域内部产生的磁滞回线显示出由于外部电场下c轴极化分量的对准,压电响应显着增加。在200°C下进行PFM扫描20小时后,未观察到书面域模式的可观察到的变化,这证实了B6TFO在此有限时间内保持了极化。这些研究证明了B6TFO薄膜在高温下用于压电应用以及在非易失性铁电存储应用中的潜力。

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