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arXiv 0909.4964cond-mat.str-el
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电荷有序反铁磁体La1.5Sr 0.5CoO 4的磁序和动力学

Magnetic order and dynamics of the charge-ordered antiferromagnet La1.5Sr0.5CoO4

L. M. Helme, A. T. Boothroyd, R. Coldea, D. Prabhakaran, C. D. Frost, D. A. Keen, L. P. Regnault, P. G. Freeman, M. Enderle, J. Kulda

摘要:

我们描述了中子散射实验进行调查的磁性秩序和动力学的半掺杂La1.5Sr0.5CoO4。这种层状钙钛矿在低于~ 800 K的温度下表现出Co2+/Co 3+电荷顺序的接近理想的棋盘图案。磁相关性在低于60 K的温度下观察到,但静态磁序仅在31 K时建立,在该温度下观察到磁化率的扭结。在升温超过31 K时,我们观察到磁相关性的变化,我们将其归因于自旋倾斜或不等价磁畴比例的变化。的磁激发谱是由一个强带延伸以上的间隙约3毫电子伏的最大能量为16毫电子伏的占主导地位。一个较弱的带存在于能量范围20-30 meV。我们表明,激发光谱是在良好的定量协议的自旋波理论的预测广义包括全磁自由度的高自旋Co 2+离子在轴向扭曲的晶体场,耦合海森堡交换相互作用。磁性秩序被发现是稳定的主导反铁磁Co2+ - Co2+的相互作用,在一条直线通过Co 3+。没有发现来自Co 3+离子的磁散射的证据,支持Co 3+在该材料中处于S = 0状态的观点。

英文摘要:

We describe neutron scattering experiments performed to investigate the magnetic order and dynamics of half-doped La1.5Sr0.5CoO4. This layered perovskite exhibits a near-ideal checkerboard pattern of Co2+/Co3+ charge order at temperatures below ~ 800 K. Magnetic correlations are observed at temperatures below ~ 60 K but static magnetic order only becomes established at 31 K, a temperature at which a kink is observed in the susceptibility. On warming above 31 K we observed a change in the magnetic correlations which we attribute either to a spin canting or to a change in the proportion of inequivalent magnetic domains. The magnetic excitation spectrum is dominated by an intense band extending above a gap of approximately 3 meV up to a maximum energy of 16 meV. A weaker band exists in the energy range 20-30 meV. We show that the excitation spectrum is in excellent quantitative agreement with the predictions of a spin-wave theory generalized to include the full magnetic degrees of freedom of high-spin Co2+ ions in an axially distorted crystal field, coupled by Heisenberg exchange interactions. The magnetic order is found to be stabilized by dominant antiferromagnetic Co2+ -- Co2+ interactions acting in a straight line through Co3+. No evidence is found for magnetic scattering from the Co3+ ions, supporting the view that Co3+ is in the S = 0 state in this material.

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