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利用穆斯堡尔谱研究 NaFeAs 中 57Fe 的局域结构和超精细相互作用。

Local structure and hyperfine interactions of 57Fe in NaFeAs studied by Mössbauer spectroscopy.

机构信息

Lomonosov Moscow State University, Moscow, 119992 Leninskie Gory, Moscow, Russia.

出版信息

J Phys Condens Matter. 2013 Aug 28;25(34):346003. doi: 10.1088/0953-8984/25/34/346003.

Abstract

Detailed 57Fe Mössbauer spectroscopy measurements on superconducting NaFeAs powder samples have been performed in the temperature range 13 K ≤ T < 300 K. The 57Fe spectra recorded in the paramagnetic range (T > TN ≈ 46 K) are discussed supposing that most of the Fe2+ ions are located in distorted (FeAs4) tetrahedra of NaFeAs phase, while an additional minor (<10%) component of the spectra corresponds to impurity or intergrowth NaFe2As2 phase with a nominal composition near NaFe2As2. Our results reveal that the structural transition (TS ≈ 55 K) has a weak effect on the electronic structure of iron ions, while at T ≤ TN the spectra show a continuous distribution of hyperfine fields HFe. The shape of these spectra is analyzed in terms of two models: (i) an incommensurate spin density wave modulation of iron magnetic structure, (ii) formation of a microdomain structure or phase separation. It is shown that the hyperfine parameters obtained using these two methods have very similar values over the whole temperature range. Analysis of the temperature dependence HFe(T) with the Bean–Rodbell model leads to ζ = 1.16 ± 0.05, suggesting that the magnetic phase transition is first order in nature. A sharp evolution of the VZZ(T) and η(T) parameters of the full Hamiltonian of hyperfine interactions near T ≈ (TN,TS) is interpreted as a manifestation of the anisotropic electron redistribution between the dxz-, dyz- and dxy-orbitals of the iron ions.

摘要

对超导 NaFeAs 粉末样品进行了详细的 57Fe Mössbauer 光谱测量,温度范围为 13 K ≤ T < 300 K。在顺磁范围(T > TN ≈ 46 K)记录的 57Fe 光谱被讨论,假设大多数 Fe2+ 离子位于 NaFeAs 相的扭曲(FeAs4)四面体中,而光谱的附加较小(<10%)部分对应于杂质或共生 NaFe2As2 相,其组成接近 NaFe2As2。我们的结果表明,结构转变(TS ≈ 55 K)对铁离子的电子结构影响较弱,而在 T ≤ TN 时,光谱显示出超精细场 HFe 的连续分布。这些光谱的形状用两种模型进行分析:(i)铁磁结构的不均匀自旋密度波调制,(ii)微畴结构或相分离的形成。结果表明,使用这两种方法获得的超精细参数在整个温度范围内具有非常相似的值。用 Bean–Rodbell 模型对 HFe(T)的温度依赖性进行分析,得到 ζ = 1.16 ± 0.05,表明磁相变本质上是一级相变。在 T ≈ (TN,TS)附近,超精细相互作用全哈密顿量的 VZZ(T)和 η(T)参数的急剧演变被解释为铁离子的 dxz、dyz 和 dxy 轨道之间的电子再分布的各向异性的表现。

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