Low temperature heat capacity of Fe1−xGax alloys with large magnetostriction

The low temperature heat capacity Cp of Fe1−xGax alloys with large magnetostriction has been investigated. The data were analyzed in the standard way using electron (γT) and phonon (βT3) contributions. The Debye temperature ΘD decreases approximately linearly with increasing Ga concentration, consistent with previous resonant ultrasound measurements and measured phonon dispersion curves. Calculations of ΘD from lattice dynamical models and from measured elastic constants C11,C12, and C44 are in agreement with the measured data. The linear coefficient of electronic specific heat γ remains relatively constant as the Ga concentration increases, despite the fact that the magnetoelastic coupling increases. Band structure calculations show that this is due to the compensation of majority and minority spin states at the Fermi level

Effect of carbon addition on the single crystalline magnetostriction of Fe-X (X = Al and Ga) alloys

The effect of carbon addition on the magnetostriction of Fe–Ga and Fe–Al alloys was investigated and is summarized in this study. It was found that the addition of carbon generally increased the magnetostriction over binary alloys of Fe–Ga and Fe–Al systems. The formation of carbide in the Fe–Ga–C alloys with a composition near D03 phase region decreased the magnetostriction drastically. Fe–Al–C and Fe–Ga–C alloys responded differently to thermal treatments; the magnetostriction in the quenched Fe–Al–C alloys is equal to or slightly lower than that of the slow cooled as is observed in binary Fe–Al alloy; in contrast, the magnetostriction is generally higher in quenched Fe–Ga–C alloys than slow cooled condition, consistent with the behavior of binary alloys of Fe–Ga. A significant increase in magnetostriction between 25% and 165% depending on the phase region in Fe–Ga–C alloys by quenching was observed in the A2+D03 two-phase region and D03 single phase region

Interplay between Fe and Nd magnetism in NdFeAsO single crystals

The structural and magnetic phase transitions have been studied on NdFeAsO single crystals by neutron and x-ray diffraction complemented by resistivity and specific heat measurements. Two low-temperature phase transitions have been observed in addition to the tetragonal-to-orthorhombic transition at T_S = 142 K and the onset of antiferromagnetic (AFM) Fe order below T_N = 137 K. The Fe moments order AFM in the well-known stripe-like structure in the (ab) plane, but change from AFM to ferromagnetic (FM) arrangement along the c direction below T* = 15 K accompanied by the onset of Nd AFM order below T_Nd = 6 K with this same AFM configuration. The iron magnetic order-order transition in NdFeAsO accentuates the Nd-Fe interaction and the delicate balance of c-axis exchange couplings that results in AFM in LaFeAsO and FM in CeFeAsO and PrFeAsO.Comment: revised; 4 pages, 3 figures; accepted for publication in Phys. Rev.

Two-dimensional magnetic interactions in LaFeAsO

Inelastic neutron scattering measurements demonstrate that the magnetic interactions in antiferromagnetic LaFeAsO are two dimensional. Spin-wave velocities within the Fe layer and the magnitude of the spin gap are similar to the AFe2As2 based materials. However, the ratio of interlayer and intralayer exchange is found to be less than ∼10−4 in LaFeAsO, very similar to the cuprates, and ∼100 times smaller than that found in AFe2As2 compounds. The results suggest that the effective dimensionality of the magnetic system is highly variable in the parent compounds of the iron arsenides and weak three-dimensional interactions may limit the maximum attainable superconducting Tc

Controlling Magnetic Order, Magnetic Anisotropy, and Band Topology in Semimetals Sr(Mn0.9Cu0.1)Sb2{\rm Sr(Mn_{0.9}Cu_{0.1})Sb_2} and Sr(Mn0.9Zn0.1)Sb2{\rm Sr(Mn_{0.9}Zn_{0.1})Sb_2}

Neutron diffraction and magnetic susceptibility studies show that orthorhombic single-crystals of topological semimetals ${\rm Sr(Mn_{0.9}Cu_{0.1})Sb_2}$ and ${\rm Sr(Mn_{0.9}Zn_{0.1})Sb_2}$ undergo three dimensional C-type antiferromagnetic (AFM) ordering of the Mn$^{2+}$ moments at $T_N = 200\pm10$ and $210\pm12$ K, respectively, significantly lower than that of the parent SrMnSb$_2$ with $T_N=297 \pm 3$ K. Magnetization versus applied magnetic field (perpendicular to MnSb planes) below $T_N$ exhibits slightly modified de Haas van Alphen oscillations for the Zn-doped crystal as compared to that of the parent compound. By contrast, the Cu-doped system does not show de Haas van Alphen magnetic oscillations, suggesting that either Cu substitution for Mn changes the electronic structure of the parent compound substantially, or that the Cu sites are strong scatterers of carriers that significantly shorten their mean free path thus diminishing the oscillations. Density functional theory (DFT) calculations including spin-orbit coupling predict the C-type AFM state for the parent, Cu-, and Zn-doped systems and identify the $a$-axis (i.e., perpendicular to the Mn layer) as the easy magnetization direction in the parent and 12.5% of Cu or Zn substitutions. In contrast, 25% of Cu content changes the easy magnetization to the $b$-axis (i.e., within the Mn layer). We find that the incorporation of Cu and Zn in SrMnSb$_2$ tunes electronic bands near the Fermi level resulting in different band topology and semi-metallicity. The parent and Zn-doped systems have coexistence of electron and hole pockets with opened Dirac cone around the Y-point whereas the Cu-doped system has dominant hole pockets around the Fermi level with a distorted Dirac cone. The tunable electronic structure may point out possibilities of rationalizing the experimentally observed de Haas van Alphen magnetic oscillations

Magnetic structure of Dy3+ in hexagonal multiferroic DyMnO3

Element specific x-ray resonant magnetic scattering (XRMS) investigations were undertaken to determine the magnetic structure of the multiferroic compound, hexagonal DyMnO3. In the temperature range from 68 K down to 8 K the Dy3+ moments are aligned and antiferromagnetically correlated in the c direction according to the magnetic representation Γ3. The temperature dependence of the observed intensity can be modeled assuming the splitting of ground-state doublet crystal-field levels of Dy3+ by the exchange field of Mn3+. XRMS together with magnetization measurements indicate that the magnetic representation is Γ2 below 8 K