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Spin frustration and orbital physics in vanadates

钒酸盐中的自旋挫败和轨道物理

基本信息

批准号：
EP/E034993/2
负责人：
J P Goff
金额：
--
依托单位：
Royal Holloway University of London
依托单位国家：
英国
项目类别：
Research Grant
财政年份：
2008
资助国家：
英国
起止时间：
2008 至无数据
项目状态：
已结题

来源：
https://gtr.ukri.org/projects?ref=EP%2FE034993%2F2
关键词：
Spin frustration orbital physics vanadates

项目摘要

The study of spin frustration and orbital physics is one of the most exciting frontiers of contemporary research in condensed matter physics. The discovery of experimental realisations of model spin-orbital systems in vanadate compounds, coupled with recent developments of time-of-flight and polarised neutron, and resonant x-ray scattering techniques at central facilities, gives unprecedented opportunities to make major contributions in this field. However, in order to take maximum advantage the provision of single-crystal samples is mandatory. The growth of single-crystal vanadates is in its infancy, but we propose to employ a PDRA who has already produced some of the largest single crystals of these compounds using the floating-zone technique. We also propose to collaborate with a leading European materials discovery laboratory employing the complementary flux growth technique, and with condensed matter theorists working in this area. First, we have discovered frustrated ferromagnetism in square-lattices with significant cross-bond exchange, in Pb2VO(PO4)2 and related materials. By chemical substitution we will be able to realise a quantum disordered phase. Entirely new excitations are predicted in the spin liquid phase, and we propose to image this behaviour very directly in inelastic neutron scattering experiments. Secondly, the perovskite orthovanadates RVO3 exhibit novel magnetic phenomena including magnetisation reversal for LaVO3, a magnetic memory effect for GdVO3, and a staircase-like magnetisation for PrVO3. Our measurements will determine the orbital ordering and orbital excitations, and will tell us about the relative importance of the quantum fluctuations of quasi-one-dimensional orbital character, versus Jahn-Teller distortions. Finally, the AV2O4 spinels have a highly frustrated pyrochlore geometry for the V ions, and for divalent A = Zn, Mg, Cd and Mn, the orbital degree of freedom comes into play. We shall compare the orbital ground states determined using resonant x-ray scattering with theoretical predictions, and measure the complex exchange interactions using inelastic neutron scattering from large single crystals.One of the primary aims of the project is to train PhD students not only in the complementary use of neutrons and x-rays in an exciting and important area of science, but also with the synthesis know-how to produce materials allowing the fullest use to be made of world-leading neutron and synchrotron facilities.

自旋阻挫和轨道物理的研究是当代凝聚态物理研究中最令人兴奋的前沿之一。钒酸盐化合物中模型自旋轨道系统的实验实现的发现，再加上飞行时间和极化中子的最新发展，以及中央设施的共振x射线散射技术，为在这一领域做出重大贡献提供了前所未有的机会。然而，为了最大限度地利用单晶样品是强制性的。单晶钒酸盐的生长还处于起步阶段，但我们建议采用PDRA谁已经产生了一些最大的单晶这些化合物使用浮区技术。我们还建议与欧洲领先的材料发现实验室采用互补通量生长技术，并与凝聚态理论家在这一领域的工作。首先，我们在Pb 2 VO（PO 4）2和相关材料中发现了具有显著交叉键交换的方形晶格中的受抑铁磁性。通过化学替代，我们将能够实现量子无序相。在自旋液相中预测了非常新的激发，我们建议在非弹性中子散射实验中非常直接地成像这种行为。其次，钙钛矿正钒酸盐RVO 3表现出新的磁性现象，包括磁化反转LaVO 3，磁记忆效应GdVO 3，和阶梯状磁化PrVO 3。我们的测量将确定轨道排序和轨道激发，并将告诉我们准一维轨道特征的量子涨落与Jahn-Teller畸变的相对重要性。最后，AV 2 O 4尖晶石具有V离子的高度受挫烧绿石几何形状，并且对于二价A = Zn、Mg、Cd和Mn，轨道自由度开始起作用。我们将用共振X射线散射确定的轨道基态与理论预测进行比较，并用大单晶的非弹性中子散射测量复杂的交换相互作用。该项目的主要目的之一是培养博士生，不仅在中子和X射线的互补使用方面，而且还具有生产材料的合成技术，从而能够最充分地利用世界领先的中子和同步加速器设施。