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铱双钙钛矿Ba(2-x)Sr(x)YIrO6的结构和磁性特性

Structural and Magnetic Properties of the Iridium Double Perovskites Ba(2-x)Sr(x)YIrO6.

作者信息

Ranjbar Ben, Reynolds Emily, Kayser Paula, Kennedy Brendan J, Hester James R, Kimpton Justin A

机构信息

School of Chemistry, The University of Sydney , Sydney, New South Wales 2006, Australia.

Australian Nuclear Science and Technology Organisation , Lucas Heights, New South Wales 2234, Australia.

出版信息

Inorg Chem. 2015 Nov 2;54(21):10468-76. doi: 10.1021/acs.inorgchem.5b01905. Epub 2015 Oct 21.

Abstract

The crystal structures of the series of ordered double perovskites Ba(2-x)Sr(x)YIrO6 (0 ≤ x ≤ 2) were refined using a combination of high-resolution synchrotron X-ray and high-intensity neutron diffraction data. The materials displayed a sequence of structures Fm3̅m(a(0)a(0)a(0)) (x = 0.6)--> I4/m(a(0)a(0)c(-)) (x = 1.0)--> I2/m(a(-)a(-)c(0)) (x = 1.4)--> P2(1)/n(a(-)a(-)c(+)) associated with increased tilting of the corner-sharing octahedra induced by increasing amount of the smaller Sr cation present. A similar sequence of transitions was induced by heating selected samples. Magnetic susceptibility measurements between 2 and 300 K showed no evidence for long-range magnetic ordering, an observation that was supported by neutron diffraction measurements, and rather strong spin-orbit coupling results in a Jeff = 0 ground state.

摘要

利用高分辨率同步辐射X射线和高强度中子衍射数据相结合的方法,对有序双钙钛矿系列Ba(2 - x)Sr(x)YIrO6(0 ≤ x ≤ 2)的晶体结构进行了精修。这些材料呈现出一系列结构:Fm3̅m(a(0)a(0)a(0))(x = 0.6)→ I4/m(a(0)a(0)c(-))(x = 1.0)→ I2/m(a(-)a(-)c(0))(x = 1.4)→ P2(1)/n(a(-)a(-)c(+)),这与随着较小的Sr阳离子含量增加而导致的共角八面体倾斜增加有关。对选定样品进行加热也会引发类似的转变序列。在2至300 K之间的磁化率测量结果表明,没有证据表明存在长程磁有序,这一观察结果得到了中子衍射测量的支持,并且相当强的自旋轨道耦合导致基态总角动量Jeff = 0。

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