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Influence of Polymorphism on the Magnetic Properties of Co5TeO8 Spinel
Inorganic Chemistry ( IF 4.6 ) Pub Date : 2021-09-08 , DOI: 10.1021/acs.inorgchem.1c01131
Stanislav Podchezertsev 1, 2 , Nicolas Barrier 1 , Alain Pautrat 1 , Emmanuelle Suard 2 , María Retuerto 3 , Jose Antonio Alonso 3 , María Teresa Fernández-Díaz 2 , Juan Rodríguez-Carvajal 2
Affiliation  

This study presents the influence of polymorphism on the magnetic properties of Co5TeO8. This compound with a spinel-like structure [Co2]A[Co3Te]BO8 was synthesized into two polymorphs: one disordered within a cubic Fdm structure, where Co2+ and Te6+ ions are randomly distributed on the octahedral B sites [the disordered polymorph can also be presented as an inverse spinel of the formula Co(Co1.5Te0.5)O4] and the other ordered with a cubic P4332 structure where Co2+ and Te6+ ions are ordered on the B sites. The macroscopic magnetic measurements showed that both polymorphs present a ferrimagnetic ordering, below ∼40 K, and a second transition is also observed at 27 K for the ordered polymorph. Neutron powder diffraction data between room temperature and 1.7 K showed as well the presence of short-range magnetic ordered clusters, which appears for both polymorphs below 200 K. At lower temperature, these short-range orders are transformed into long-range ferrimagnetic orders. Below TC = 40 K, the colinear ferrimagnetic structure of the disordered polymorph is described with the I41/amd′ space group. The ordered polymorph undergoes an incommensurate ferrimagnetic spiral spin ordering below TC1 = 45 K, followed by a second magnetic phase transition at TC2 = 27 K. This last transition is associated with the emergence of an additional ferrimagnetic component and an abrupt change in the magnitude of the magnetic propagation vector k = [0, 0, γ] from γ = 0.086 at T = 30 K to γ ≈ 0.14 in the range between 27 and 1.7 K. The magnetic symmetry of the ordered polymorph is described with the P43(00γ)0 magnetic superspace group. We evidenced that the ordering of Co2+/Te6+ on the B sites changes all of the Co–Co and Co–O distances and thus all JAB, JAA, and JBB exchange interactions, between the A and B sites, which are able to stabilize the incommensurate spin modulation in the ordered polymorph.

中文翻译:

多晶型对Co5TeO8尖晶石磁性的影响

本研究介绍了多晶型对 Co 5 TeO 8磁性能的影响。这种具有尖晶石状结构 [Co 2 ] A [Co 3 Te] B O 8 的化合物被合成为两种多晶型物:一种在立方Fdm结构内无序,其中 Co 2+和 Te 6+离子随机分布在八面体 B 位点 [无序多晶型也可以表示为式 Co(Co 1.5 Te 0.5 )O 4的反尖晶石] 和另一个有序的具有立方P 43 32 结构,其中 Co 2+和 Te 6+离子在 B 位点排列。宏观磁性测量表明,两种多晶型物都呈现亚铁磁有序,低于~40 K,并且在 27 K 处也观察到有序多晶型物的第二次转变。室温和 1.7 K 之间的中子粉末衍射数据也表明存在短程磁性有序簇,这对于低于 200 K 的两种多晶型物都会出现。在较低温度下,这些短程有序转变为长程亚铁磁序。在T C = 40 K 以下,无序多晶型物的共线亚铁磁结构描述为I 4 1 / am 'd ′ 空间群。有序多晶型在T C1 = 45 K以下经历不相称的亚铁磁螺旋自旋排序,然后在T C2 = 27 K处发生第二次磁相变。最后一次相变与额外亚铁磁成分的出现和磁传播矢量的大小k = [0, 0, γ] 从T = 30 K 时的γ = 0.086到 27 到 1.7 K 范围内的 γ ≈ 0.14。有序多晶型物的磁对称性用P 4描述3 (00γ)0 磁超空间群。我们证明了 Co 2+ /Te 6+的顺序B 位点上的所有 Co-Co 和 Co-O 距离都会改变,因此A 和 B 位点之间的所有J ABJ AAJ BB交换相互作用都能够稳定有序的不相称的自旋调制多晶型。
更新日期:2021-09-20
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