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在具有三角晶体结构的 5d 磁性氧化物 Ca3LiOsO6 的高磁有序温度方面:密度泛函分析。

On the high magnetic-ordering temperature of the 5d magnetic oxide Ca3LiOsO6 crystallizing in a trigonal crystal structure: density functional analysis.

机构信息

Department of Applied Physics, Nanjing University of Science and Technology, Nanjing, Jiangsu 210094, People's Republic of China.

出版信息

Inorg Chem. 2011 May 2;50(9):4182-6. doi: 10.1021/ic200305a. Epub 2011 Mar 25.

Abstract

The 5d magnetic oxide Ca(3)LiOsO(6) has a trigonal arrangement of its LiOsO(6) chains parallel to the c-direction and hence has triangular arrangements of high-spin Os(5+) (d(3)) ions but exhibits no spin frustration and undergoes a long-range antiferromagnetic ordering at a high temperature. The origin of this apparently puzzling observation was examined by evaluating the nearest-neighbor Os-O···O-Os spin exchange interactions of Ca(3)LiOsO(6) on the basis of density functional calculations. Our study shows that, of the two nearest-neighbor interchain spin exchanges, one dominates over the other and that the intrachain spin exchange and the dominating interchain spin exchange are strong and form a three-dimensional antiferromagnetic spin lattice with no spin frustration, which is responsible for the long-range antiferromagnetic ordering of Ca(3)LiOsO(6) at high temperature. In determining the strengths of the Os-O···O-Os exchange interactions of Ca(3)LiOsO(6), the Li(+) and Ca(2+) ions of the O···Li(+)···O and O···Ca(2+)···O linkages are found to play only a minor role.

摘要

5d 磁性氧化物 Ca(3)LiOsO(6) 中 LiOsO(6) 链沿 c 方向呈三角排列,因此具有高自旋 Os(5+)(d(3))离子的三角排列,但不表现出自旋受挫,并在高温下经历长程反铁磁有序。通过基于密度泛函计算评估 Ca(3)LiOsO(6) 的最近邻 Os-O···O-Os 自旋交换相互作用,研究了这一明显令人费解的观察结果的起源。我们的研究表明,在两个最近邻链间自旋交换中,一个占主导地位,而链内自旋交换和主导的链间自旋交换很强,并形成一个没有自旋受挫的三维反铁磁自旋晶格,这是导致 Ca(3)LiOsO(6) 在高温下长程反铁磁有序的原因。在确定 Ca(3)LiOsO(6) 的 Os-O···O-Os 交换相互作用强度时,发现 O···Li(+)···O 和 O···Ca(2+)···O 键合的 Li(+) 和 Ca(2+) 离子仅起次要作用。

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