Er3+/BiFeO3纳米催化剂的电场驱动应变和多铁性

Monika , Praveen Kumar , Varun Sangwan , Amarjeet , Mahendra , Abhishek Saxena , Shakshi Chauhan
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摘要

本文研究了采用固态法制备的Er3+/BiFeO3纳米催化剂的结构、阻抗、电应变和磁性能。XRD (x射线衍射)图表明,BFO具有扭曲的菱形结构(空间群R3c),随着a位Er掺杂量的增加,平均畴尺寸从38.4 nm改变到23.7 nm。利用FeSEM和EDS对其形态和元素映射进行了研究。在2 MHz至10 Hz的频率范围内,在不同温度下进行了复杂阻抗和介电特性的研究。介电常数ε′随频率的增加而显著降低,随温度的升高而显著升高。峰间应变(SP、SN)和γs(不对称因子)分别在0.89 ~ 3.32%、0.758 ~ 3.124%和15.4 ~ 34.3%范围内显著,应变记忆值最高(Sme%) 0.362。通过P-E磁滞回线和M-H磁滞回线检测,Er3+离子的掺杂导致饱和极化(Ps)从0.781增加到1.884 μC/cm2,饱和磁化(Ms)从0.764增加到3.27 emu/gm。带隙工程和表面反应性的改善使得光催化降解效率从64.8%提高到81.4%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Electric field driven strain and multiferroic properties of Er3+/BiFeO3 nano-catalyst

Electric field driven strain and multiferroic properties of Er3+/BiFeO3 nano-catalyst
In this work, we examined the structural, impedance, electro-strain, magnetic properties of Er3+/BiFeO3 nanocatlyst prepared via solid state route. The XRD (X-ray Diffraction) pattern reveals that the BFO has a distorted rhombohedral structure (space group R3c) with average domain size was altered from 38.4 nm to 23.7 nm as Er doping increases on the A-site. The morphological and elemental mapping studies were studied by using FeSEM and EDS. The complex impedance and dielectric investigations were conducted at various temperatures in the frequency range 2 MHz to 10 Hz. The dielectric constant (ε') has been observed to significantly decreases as the frequency increases and to rise as temperature increases. A significant peak-to-peak strain (SP and SN) and γs (factor of asymmetry) were recorded in the ranges of 0.89–3.32 %, 0.758–3.124 %, and 15.4–34.3 %, correspondingly, with the highest strain memory value (Sme%) 0.362. The doping of Er3+ ions resulted in an extensive augment in saturation polarization (Ps) from 0.781 to 1.884 μC/cm2 and saturation magnetization (Ms) from 0.764 to 3.27 emu/gm, as examined via the P-E hysteresis and M-H hysteresis loops, respectively. Band gap engineering and improved surface reactivity with Er doping led to an improvement in photo-catalytic degradation efficiencies from 64.8 % to 81.4 %.
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