Amit Mondal, Riju Dey, Andreja Jelen, Primož Koželj, Sandip Kumar Kuila, Rahul Pan, Stanislav Vrtnik, Jože Luzar, Magdalena Wencka, Julia Petrović, Peter Mihor, Zvonko Jagličić, Anton Meden, Partha Pratim Jana* and Janez Dolinšek*,
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The alloys crystallize in two chiral enantiomorphic space groups <i>P</i>6<sub>2</sub> and <i>P</i>6<sub>4</sub>, where the basic atomic polyhedron of the chiral structure is an icosahedron and the neighboring icosahedra share vertices to form an infinitely long double helix along the hexagonal axis (like in the δ-Co<sub>2.5</sub>Zn<sub>17.5</sub> parent binary phase). The alloys are pure δ-phase up to the Mn content <i>x</i> ≈ 3.5. The Mn atoms partially substitute Zn atoms at particular crystallographic sites located on the icosahedra. The study of magnetism was performed on the Co<sub>2.5</sub>Zn<sub>17.1</sub>Mn<sub>0.4</sub> alloy with the lowest Mn content. Contrary to the expectation that structural chirality may induce the formation of a nontrivial magnetic state, a spin glass state with no relation to the structural chirality was found. The magnetic sublattice contains all of the necessary ingredients (randomness and frustration) for the formation of a spin glass state. Typical out-of-equilibrium dynamic phenomena of a spin system with broken ergodicity were detected below the spin freezing temperature <i>T</i><sub>f</sub> ≈ 8 K.</p><p >In a search for structural chirality-induced nontrivial magnetic states, we have synthesized the δ-Co<sub>2.5</sub>Zn<sub>17.5−<i>x</i></sub>Mn<sub><i>x</i></sub> (<i>x</i> = 0.4−3.5) pseudo-binary chiral alloys and determined their crystal structures, Mn substitution pattern, and magnetic properties. 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引用次数: 0
摘要
我们采用高温固态合成路线合成了10种不同成分的δ-Co2.5Zn17.5-xMnx(x = 0.4-3.5)假二元合金,确定了它们的晶体结构和锰的取代模式,并估算了δ相的存在范围。合金在两个手性对映空间群 P62 和 P64 中结晶,其中手性结构的基本原子多面体为二十面体,相邻的二十面体共享顶点,沿六方轴形成无限长的双螺旋(与 δ-Co2.5Zn17.5 母体二元相类似)。在锰含量 x ≈ 3.5 以下,合金为纯δ相。锰原子部分取代了位于二十面体上特定晶体学位点上的锌原子。对锰含量最低的 Co2.5Zn17.1Mn0.4 合金进行了磁性研究。与结构手性可能诱导形成非三重磁态的预期相反,研究发现了一种与结构手性无关的自旋玻璃态。磁性子晶格包含形成自旋玻璃态的所有必要成分(随机性和挫折感)。在自旋冻结温度 Tf ≈ 8 K 以下,检测到了具有破碎遍历性的自旋系统的典型失衡动态现象。
Double Helix of Icosahedra Structure and Spin Glass Magnetism of the δ-Co2.5Zn17.5–xMnx (x = 0.4–3.5) Pseudo-Binary Alloys
We have synthesized δ-Co2.5Zn17.5–xMnx (x = 0.4–3.5) pseudo-binary alloys of 10 different compositions by a high-temperature solid-state synthetic route, determined their crystal structures and the Mn substitution pattern, and estimated the existence range of the δ-phase. The alloys crystallize in two chiral enantiomorphic space groups P62 and P64, where the basic atomic polyhedron of the chiral structure is an icosahedron and the neighboring icosahedra share vertices to form an infinitely long double helix along the hexagonal axis (like in the δ-Co2.5Zn17.5 parent binary phase). The alloys are pure δ-phase up to the Mn content x ≈ 3.5. The Mn atoms partially substitute Zn atoms at particular crystallographic sites located on the icosahedra. The study of magnetism was performed on the Co2.5Zn17.1Mn0.4 alloy with the lowest Mn content. Contrary to the expectation that structural chirality may induce the formation of a nontrivial magnetic state, a spin glass state with no relation to the structural chirality was found. The magnetic sublattice contains all of the necessary ingredients (randomness and frustration) for the formation of a spin glass state. Typical out-of-equilibrium dynamic phenomena of a spin system with broken ergodicity were detected below the spin freezing temperature Tf ≈ 8 K.
In a search for structural chirality-induced nontrivial magnetic states, we have synthesized the δ-Co2.5Zn17.5−xMnx (x = 0.4−3.5) pseudo-binary chiral alloys and determined their crystal structures, Mn substitution pattern, and magnetic properties. A spin glass state with typical broken ergodicity phenomena was found, being in no relation to the structural chirality.
期刊介绍:
Inorganic Chemistry publishes fundamental studies in all phases of inorganic chemistry. Coverage includes experimental and theoretical reports on quantitative studies of structure and thermodynamics, kinetics, mechanisms of inorganic reactions, bioinorganic chemistry, and relevant aspects of organometallic chemistry, solid-state phenomena, and chemical bonding theory. Emphasis is placed on the synthesis, structure, thermodynamics, reactivity, spectroscopy, and bonding properties of significant new and known compounds.