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Register a new userMagnetism of PrFeAsO parent compound for iron-based superconductors: Mossbauer spectroscopy study
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Added by
Krzysztof Ruebenbauer
Publication date
2016
fields
Physics
and research's language is
English
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Moessbauer spectroscopy measurements were performed for the temperature range between 4.2 K and 300 K in a transmission geometry applying 14.41-keV resonant line in 57Fe for PrFeAsO the latter being a parent compound of the iron-based superconductors belonging to the 1111 family. It was found that an itinerant 3d magnetic order develops at about 165 K and it is accompanied by an orthorhombic distortion of the chemical unit cell. A complete longitudinal 3d incommensurate spin density wave (SDW) order develops at about 140 K. Transferred hyperfine magnetic field generated by the praseodymium magnetic order on iron nuclei is seen at 12.8 K and below, i.e., below magnetic order of praseodymium magnetic moments. It is oriented perpendicular to the field of SDW on iron nuclei. The shape of SDW is almost rectangular at low temperatures and it transforms into roughly triangular form around nematic transition at about 140 K. Praseodymium magnetic order leads to the substantial enhancement of SDW due to the large orbital contribution to the magnetic moment of praseodymium. A transferred field indicates presence of strong magnetic susceptibility anisotropy in the [b-c] plane while following rotation of praseodymium magnetic moments in this plane with lowering temperature. It was found that nematic phase region is a region of incoherent spin density wavelets typical for a critical region.
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A review of the magnetism in the parent compounds of the iron-based superconductors is given based on the transmission Moessbauer spectroscopy of 57Fe and 151Eu. It was found that the 3d magnetism is of the itinerant character with varying admixture of the spin-polarized covalent bonds. For the 122 compounds a longitudinal spin density wave (SDW) develops. In the case of the EuFe2As2 a divalent europium orders antiferromagnetically at much lower temperature as compared to the onset of SDW. These two magnetic systems remain almost uncoupled one to another. For the non-stoichiometric Fe(1+x)Te parent of the 11 family one has a transversal SDW and magnetic order of the interstitial iron with relatively high and localized magnetic moments. These two systems are strongly coupled one to another. For the grand parent of the iron-based superconductors FeAs one observes two mutually orthogonal phase-related transversal SDW on the iron sites. There are two sets of such spin arrangements due to two crystallographic iron sites. The FeAs exhibits the highest covalency among compounds studied, but it has still a metallic character.
The compound BaFe2Se3 (Pnma) has been synthesized in the form of single crystals with the average composition Ba0.992Fe1.998Se3. The Moessbauer spectroscopy used for investigation of the valence states of Fe in this compound at temperature ranging from 4.2 K till room temperature revealed the occurrence of mixed-valence state for iron. The spectrum is characterized by sharply defined electric quadrupole doublet above magnetic ordering at about 250 K. For the magnetically ordered state one sees four iron sites at least and each of them is described by separate axially symmetric electric field gradient tensor with the principal component making some angle with the hyperfine magnetic field. They form two groups occurring in equal abundances. It is likely that each group belongs to separate spin ladder with various tilts of the FeSe4 tetrahedral units along the ladder. Two impurity phases are found, i.e., superconducting FeSe and some other unidentified iron-bearing phase being magnetically disordered above 80 K. Powder form of BaFe2Se3 is unstable in contact with the air and decomposes slowly to this unidentified phase exhibiting almost the same quadrupole doublet as BaFe2Se3 above magnetic transition temperature.
57Fe and 151Eu Moessbauer spectra were obtained versus temperature for Eu0.57Ca0.43Fe2As2 compound with 3d and 4f magnetic order and Eu0.73Ca0.27(Fe0.87Co0.13)2As2 re-entrant superconductor, where the finite resistivity reappears while approaching the ground state. They were compared with previously obtained spectra for parent compounds EuFe2As2 and CaFe2As2. It was found that substitution beyond the Fe-As layers does not lead to the rotation (canting) of the Eu2+ magnetic moments and does not generate Eu3+ states. On the other hand, re-entrant superconductor exhibits rotation (canting) of the Eu2+ moments on the c-axis of the unit cell leading to the transferred hyperfine magnetic field on iron nuclei. Divalent europium orders magnetically within the bulk of the re-entrant superconducting phase. The re-entrant superconductor remains in the inhomogeneous state close to the ground state with about 27 % of the volume being free of 3d magnetism, while the remainder exhibits weak spin density wave. Those two regions slightly differ by the electric field gradient and electron density on iron nuclei.
We elucidate the existing controversies in the newly discovered K-doped iron selenide (KxFe2-ySe2-z) superconductors. The stoichiometric KFe2Se2 with surd2timessurd2 charge ordering was identified as the parent compound of KxFe2-ySe2-z superconductor using scanning tunneling microscopy and spectroscopy. The superconductivity is induced in KFe2Se2 by either Se vacancies or interacting with the anti-ferromagnetic K2Fe4Se5 compound. Totally four phases were found to exist in KxFe2-ySe2-z: parent compound KFe2Se2, superconducting KFe2Se2 with surd2timessurd5 charge ordering, superconducting KFe2Se2-z with Se vacancies and insulating K2Fe4Se5 with surd5timessurd5 Fe vacancy order. The phase separation takes place at the mesoscopic scale under standard molecular beam epitaxy condition.
We investigate the transient electronic structure of BaFe2As2, a parent compound of iron-based superconductors, by time- and angle-resolved photoemission spectroscopy. In order to probe the entire Brillouin zone, we utilize extreme ultraviolet photons and observe photoemission intensity oscillation with the frequency of the A1g phonon which is antiphase between the zone-centered hole Fermi surfaces (FSs) and zone-cornered electron FSs. We attribute the antiphase behavior to the warping in one of the zone-centered hole FSs accompanying the displacement of the pnictogen height, and find that this displacement is the same direction as that induced by substitution of P for As, where superconductivity is induced by a structural modification without carrier doping in this system.
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