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XRD and Mössbauer spectroscopy study of Ho doped BiFeO3

机译:掺HoBiFeO3的XRD和穆斯堡尔谱研究

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摘要

The structural and magnetic properties of Ho substituted BiFeO3 (BHFO) have been investigated using 57Fe Mössbauer spectroscopy and X-Ray diffraction (XRD) as a function of temperature. The Mössbauer spectrum obtained at room temperature for the as-synthesized BHFO sample exhibits broadened features due to the hyperfine field distributions related to the local variation of the neighbourhood of Fe and the magnetic hyperfine splitting patterns are indicative of magnetic ordering, mostly probably screwed or slightly antiferromagnetic. The spectrum was fitted with two superimposed asymmetric sextets, with similar hyperfine magnetic fields of Bhf1 = 48.0(1) T and Bhf2 = 49.0(1) T, corresponding to rhombohedral BFO. The hyperfine fields of the magnetic components decreased systematically with increasing temperature to a ‘field distribution’ just below the Néel temperature, TN ~ 600 K. At temperatures above 600 K, the spectral line associated with the Bi25FeO40 impurity phase dominates the spectra. This phase is confirmed by XRD measurements. From the temperature dependence of the site populations of the spectral components an average Debye temperature of θ D = 240(80) K has been estimated.
机译:使用57FeMössbauer光谱和X射线衍射(XRD)作为温度的函数,研究了Ho取代的BiFeO3(BHFO)的结构和磁性。合成后的BHFO样品在室温下获得的Mössbauer谱显示出较宽的特征,这是由于与Fe邻域的局部变化有关的超精细场分布,并且磁性超细分裂模式表明磁性有序,主要可能是旋拧或略微反铁磁。该光谱用两个叠加的不对称六重音拟合,具有类似的超细磁场Bhf1 = 48.0(1)T和Bhf2 = 49.0(1)T,对应于菱形BFO。磁性成分的超精细场会随着温度的升高而系统地降低,直至“场分布”恰好低于Néel温度TN〜600K。在600 K以上的温度下,与Bi25FeO40杂质相相关的光谱线占主导地位。此阶段已通过XRD测量确认。根据光谱分量的现场温度对温度的依赖性,可以估算出平均德拜温度为θD = 240(80)K。

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  • 来源
    《Hyperfine Interactions》 |2013年第3期|83-88|共6页
  • 作者单位

    School of Physics University of the Witwatersrand">(1);

    School of Physics University of the Witwatersrand">(1);

    DST/NRF Centre of Excellence in Strong Materials University of the Witwatersrand">(2);

    DST/NRF Centre of Excellence in Strong Materials University of the Witwatersrand">(2);

    School of Physics University of KwaZulu-Natal">(3);

    DST/NRF Centre of Excellence in Strong Materials University of the Witwatersrand">(2);

    School of Chemistry University of the Witwatersrand">(4);

    School of Physics University of the Witwatersrand">(1);

    School of Physics University of the Witwatersrand">(1);

    DST/NRF Centre of Excellence in Strong Materials University of the Witwatersrand">(2);

    Institute of Materials Science Acharya Vihar">(5);

    School of Physics University of the Witwatersrand">(1);

    DST/NRF Centre of Excellence in Strong Materials University of the Witwatersrand">(2);

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