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Phase transition in rubidium carnallite doped with VO2+ by EPR method

机译:EPR法掺杂VO2 +的car钠盐岩的相变

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This work deals with EPR investigations of VO2+ doped rubidium carnallite. Vanadyl ion in some hosts e.g. NH4Cl and Mg(ClO4).6H2O etc. shows a rotatory behaviour, while in hosts like alums, sulphates, Tutton salts etc., it shows preferential orientation giving angle-dependent spectra. In the present host RbMgCl3.6H2O, the VO2+ shows an isotropic angle independent eight line hyperfine spectrum. It has already been reported that Mn2+ substitutes Mg2+ in NH4MgCl.6H2O giving two distinct EPR spectra having angular variation. But in the present work the spectra of VO2+ in RbMgCl3.6H2O does not show preferred orientation. This behaviour occurs due to VO2+ undergoing a rapid tumbling motion in the crystalline lattice. It has been also found that when the temperature is lowered to LNT, fast reorientations of V-O bond act progressively hindered and the anisotropies in and tensors are not averaged out and get reflected but it is angular independent. After analysing and comparing the spectrum it is found that VO2+ shows ‘liquid like’ behaviour in RbMgCl3.6H2O.
机译:这项工作涉及对VO2 +掺杂的car钠盐岩的EPR研究。一些宿主中的钒离子例如NH4Cl和Mg(ClO4).6H2O等表现出旋转行为,而在明矾,硫酸盐,图顿盐等主体中,它表现出优先的取向,从而给出与角度相关的光谱。在本宿主RbMgCl3.6H2O中,VO2 +显示出与各向同性角无关的八线超精细光谱。已有报道说,Mn2 +替代了NH4MgCl.6H2O中的Mg2 +,给出了两个具有角度变化的不同EPR光谱。但是在目前的工作中,RbMgCl3.6H2O中VO2 +的光谱没有显示出较好的取向。由于VO2 +在晶格中快速翻滚而发生这种现象。还已经发现,当温度降低到LNT时,V-O键的快速重新取向逐渐受到阻碍,且张量和张量中的各向异性没有被平均化并得到反映,但它与角度无关。在分析和比较光谱之后,发现VO2 +在RbMgCl3.6H2O中表现出“类似液体”的行为。

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