Magnetic properties of metallic glasses of the type Fe80−x Pd x B20 and Fe80−x Pt x B20

Amorphous alloys of the type Fe_80???xPd_xB₂₀ and type Fe_80???xPt_xB₂₀ for 0?≤?x?≤?50 have been investigated by means of ⁵⁷Fe Mössbauer spectroscopy and magnetisation measurements in temperatures from 4.2 up to 300 K. Curie temperatures and crystallisation temperatures are found by DTMG-DTA method. Mössbauer spectroscopy magnetic field is observed to visible increase for x?=?1 and 1.5% at room temperature for Pd, while a decrease is observed for higher x values. Curie temperature for Pd alloys has a maximum at x?=?4 with T _C?=?753 K, which supports enforcing influence of Pd at low concentrations of Pd for magnetic interactions. We discuss different explanations for these measurements and compare with other findings for high Pd concentrations and alloys with Pt instead of Pd.     

Fe–Ag granular multilayers and heterostructures studied in applied magnetic field

An (0.2 nm ⁵⁷Fe / 2.6 nm Ag)₇₅ granular multilayer sample and heterostructures with additional continuous Fe layers in different sequences were studied in magnetic field applied at different temperatures. The broadening of the superparamagnetic lines was found to be very similar for the three samples in applied fields both parallel and perpendicular to the sample plane. While the layer sequence has no significant effect on the superparamagnetic properties, the continuous magnetic layers follow a different approach to saturation in perpendicular magnetic fields.     

57Fe Mössbauer and magnetic studies of DyFe12−x Ta x compounds

Refinements of the X-ray diffraction patterns show that DyFe_12?x Ta _x compounds with x = 0.5–0.7 crystallise in the ThMn₁₂-type structure and that the Ta atoms occupy the 8i sites. Spin reorientations have been detected by ac magnetic susceptibility for all compounds below room temperature. First the moments shift direction from easy axis to easy cone at T _sr1, then to easy plane at T _sr2. Both T _sr1 and T _sr2 increase with increasing Ta content up to x = 0.65 before decreasing with further increase in Ta content. Analyses of the Mössbauer spectra indicate that the individual Fe site hyperfine fields derived at 4.5 K for DyFe_11.35Ta_0.65 are B _hf = 37.4 T, 32.2 T and 27.6 T for the 8i, 8j and 8f sites, respectively.     

Observation of magnetic splitting in XPS MnL-spectra of Co2MnSn and Pd2MnSn Heusler alloys

The XPS MnL-spectra of Co₂MnSn, a nearly half-metallic ferromagnet (HMF) and Pd₂MnSn were investigated. The most drastical feature of the spectra observed is the well-defined magnetic splitting of the Mn 2p _3/2 , 2p _1/2 lines. This gives direct evidence of the existence of well-defined local magnetic moments in Heusler alloys in comparison with other itinerant-electron ferromagnets. The calculations of Mn2p XPS spectra of these materials were carried out using a fully relativistic generalization of the one-step model of photoemission and show excellent agreement with experiment. Received: 31 October 1997 / Received in final form: 28 November 1997 / Accepted: 18 December 1997     

A Mössbauer study of the silica-like structures of FePO4 and (Al0.67Fe0.33)PO4

Summary Samples of FePO₄ and (Al_0.67Fe_0.33)PO₄ have been investigated by M?ssbauer spectroscopy. The data obtained on quadruple splittings are in agreement with neutron scattering and XRD data on (Al, Fe)O₄ tetrahedra structures.     

Creation of ferromagnetic properties of V–Fe and Zr–Fe alloys by hydrogen absorption

The results of investigations of V_1?y Fe _y H _x and Zr_1?y Fe _y H _x alloys by ⁵⁷Fe Mössbauer spectroscopy are presented and discussed in view of hydrogen ability to create ferromagnetic properties of the alloy. The results indicate two different possibilities of hydrogen influence on the hyperfine magnetic field. Hydrogen absorption causes the ferromagnetic behaviour of the alloys at significant lower iron concentration compared to the concentration of magnetic transition in binary alloys. The main reason for such behaviour is the anisotropic lattice expansion in hydrogenated V–Fe and Zr–Fe alloys as well as the decomposition of paramagnetic Zr-rich intermetallic compounds in the aftermath of the strong electron affinity of hydrogen for zirconium. These trends give rise to growth of magnetic clusters of Fe atoms so strong that they can participate in the overall magnetic properties of the system under investigation.     

Debye temperature and magnetic ordering in K x Ba1−x Fe2S3

⁵⁷Fe Mössbauer measurements are reported for the series K _x Ba_1?x Fe₂S₃, x ≤ 0.3, at temperatures between 4.2 K ≤ T ≤ 294 K. A decrease of the Debye temperature from 435 to 405 K with x, indicates a weakening of the stiffness of the Fe sublattice. The ordering temperatures, taken from the appearance of magnetic hyperfine splitting in the spectra, are approximately 40 K lower for x ≥ 0.1. The values of the centre shift and the small temperature dependence of the quadrupole splitting strongly supports that similar to the border compound BaFe₂S₃ also the K containing samples should be characterised as mixed valence compounds.     

Mössbauer spectroscopy study of spin structure and its in-field and temperature dynamics in B2 ordered Fe(Al) alloys

The experimental data from Mössbauer spectroscopy and magnetic measurements are presented as functions of the temperature and external magnetic field for a B2-type ordered Fe ₆₆ Al ₃₄ alloy.     

Antiferromagnetism in double-layered perowskitic oxides SrLa2Fe2O7 and BaLa2Fe2O7

Il Nuovo Cimento D - Two double-layered perowskitic compounds have been investigated by XRD analysis and Mössbauer spectroscopy. The experimental data allow the conclusion that magnetization...     

Mössbauer studies of hyperfine fields in disordered Fe2CrAl

Heusler-like alloy Fe₂CrAl was prepared and studied. Structure determination was done by X-ray. The structure was found to conform to the B₂ type. Magnetic hyperfine fields in this sample were studied by the Mössbauer effect. The Mössbauer spectra were recorded over a range of temperature from 40 to 296 K. The Mössbauer spectra showed the co-existence of a paramagnetic part with a magnetic hyperfine portion at all recorded temperatures. Even with the distribution in the magnetic hyperfine field, the average hyperfine field follows the (T/T _c)^3/2 law. The paramagnetic part of the hyperfine field is explained in terms of the clustering of Cr atoms.     

A non-magnetic Fe probe of multiple magnetic phase transitions in RMn2Si2−x Ge x,R=rare earth

Summary Dilute⁵⁷Fe M?ssbauer-spectroscopy studies of RMn₂X₂ (X=Si and/or Ge, R=La, Ce, Pr, Nd, Sm, Eu and Gd) at 4.2 to 650 K yield the following results: Fe in RMn₂X₂ does not carry a magnetic moment. It reveals the magnetic order in the Mn and R sublattices through transferred hyperfine fields (∼100 kOe). The compounds LaMn₂Si₂, LaMn₂Ge₂, CeMn₂Ge₂, PrMn₂Ge₂, NdMn₂Ge₂ and SmMn₂Ge₂, known to be ferromagnets withT _c=300–350 K, are antiferromagnetically ordered above their correspondingT _c. TherT _N values extend from 385 K (SmMn₂Ge₂) to 470 K (LaMn₂Si₂). At the ferromagnetic-antiferromagnetic phase transition, a sharp reorientation of the Mn magnetic moments relative to the crystalline axes occurs. In RMn₂Si_2−x Ge _x with intermediatex values, the Ge is much more dominant in determining the magnetic properties of the Mn sublattice. While PrMn₂Si₂ is an antiferromagnet (T _N=365 K) and PrMn₂Ge₂ is a ferromagnetantiferromagnet (T _c=328 K,T _N=415 K), we find that in PrMn₂SiGe, the magnetic behaviour is similar to that in pure PrMn₂Ge₂,T _c=305 K andT _N=395 K. Paper presented at ICAME-95, Rimini, 10–16 September 1995.     

Magnetic properties of the mechanically alloyed Fe0.9-xMn0.1Alx system

Samples of nominal composition Fe_0.9-xMn_0.1Al_x (0.1 ? x ? 0.5) were prepared by mechanical alloying starting from pure elements. Milling times of 24, 72 and 144 h were considered. The magnetic properties of the samples were studied by using ⁵⁷Fe Mössbauer spectroscopy, vibrating sample magnetometry and magnetic susceptibility measurements. The phase distribution was determined from X-ray diffractometry. The so obtained results evidence a strong dependence on the milling time and Al concentration of the room-temperature hyperfine field distributions and coercive forces. The susceptibility measurements in the range of temperature between 10 K and 180 K suggest the occurrence of different types of transitions as the temperature is increased: (a) from a ferromagnetic to a paramagnetic phase, (b) from a reentrant spin-glass phase to a ferromagnetic one and (c) from spin-glass to a paramagnetic phase. These transitions are also strongly influenced by the milling time and the Al concentration.     

Magnetotransport and magnetic properties of sulfospinels Zn x Fe1−x Cr2S4

Cr-based chalcogenide spinels, which do not have heterovalency and distortion-induced ions such as manganese oxides with perovskite structure, have demonstrated the existence of colossal magnetoresistance. In order to investigate the magnetotransport phenomena and magnetic properties of sulfospinels Zn _x Fe_1?x Cr₂S₄, polycrystalline Zn _x Fe_1?x Cr₂S₄ samples were synthesized in the 0?≤?x?≤?0.2 range by a solid reaction method. The crystal structure for x?=?0.05, 0.1, and 0.2 turned out to be cubic at room temperature by X-ray diffraction measurement. In magnetoresistance measurement, Zn _x Fe_1?x Cr₂S₄ samples indicate that this system is semiconducting below about 150 K. The temperature of maximum magnetoresistance is almost consistent with Curie temperature. The isomer shift and the electric quadrupole shift of Zn _x Fe_1?x Cr₂S₄ samples by Mössbauer experiment show that Fe²⁺ ions occupy the tetrahedral site in the spinel structure. As the Zn ions are substituted for Fe ions, the Jahn–Teller relaxation slows down and the electric quadrupole shift increases. The magnetotransport phenomena of Zn _x Fe_1?x Cr₂S₄ is related to Jahn–Teller effect and half-metallic electronic structure, which are different from the double exchange interactions of the manganite La–Ca–Mn–O system or the triple exchange interactions of sulfospinel Cu _x Fe_1?x Cr₂S₄.     

Time-dependent absorption of gamma-radiation under high-frequency magnetic excitation of 57Fe

Summary We have studied the time dependence of M?ssbauer absorption in a magnetically soft sample of Fe₁₈Ni₈₂ permalloy under the influence of a radio-frequency (r.f.) magnetic field. Absorption was measured as a function of the r.f. field phase at specific gamma-ray energies. We have shown that measuring the time dependence of absorption makes it possible to differentiate between purely magnetic and magnetoacoustic modulation mechanisms even in cases where clear distinction is not visible in conventional energy domain spectra. Paper presented at ICAME-95, Rimini, 10–16 September 1995.     

Magnetic properties of nanostructured spinel ferrites and nanocomposite Nd2Fe114B/α-Fe permanent magnets

This paper presents some of the important magnetic properties of the nanostructured spinel ferrites such as Ni_0.5Zn_0.5Fe₂O₄ and Mn_0.67Zn_0.33Fe₂O₄ and also that of the nanocomposite Nd₂Fe₁₄B/α-Fe permanent magnetic material. The increase in the magnetic transition temperature of Ni-Zn ferrite from 538 K in the bulk state to 592 K when the grain size is reduced to 16 nm is correlated to the enhancement in the AB superexchange interaction strength because of an increase in the magnetic ion concentration in the A-site on milling, as shown by the EXAFS and in-field Mössbauer studies. The particle size has been tailor-made by varying the concentration of the oxidant in the case of Mn-Zn ferrite. The critical particle size for the superparamagnetic limit has been found to be 25 nm with an effective magnetic anisotropy constant of 7.78 kJ m^?3 which is about an order of magnitude higher than that of the bulk ferrite. The exchange coupling is found to be strengthened in the nanocomposite magnet Nd₂Fe₁₄B/α-Fe, when the grain boundary anisotropy is removed by thermal annealing and thus facilitating the enhancement of the energy product     

Surface properties of Fe76Mo8Cu1B15 alloy after annealing

NANOPERM-type alloy Fe₇₆Mo₈Cu₁B₁₅ is investigated in amorphous and in partially crystallized state. Samples were prepared by 1 h isothermal annealing in vacuum at temperatures ranging from 330°C up to 700°C. Bulk and surface microstructural characteristics were studied using transmission and conversion electron Mössbauer effect techniques, respectively. Surface features were checked by the help of atomic force microscopy. Presence of nanocrystalline bcc-Fe phase was detected during the first crystallization stage. The crystallization process starts at 450°C and it is more pronounced in surface regions than in the bulk. With progressing crystallization, hyperfine parameters especially of the amorphous residual phase are altered. Distinctions in surface morphology are revealed between wheel and air side of the ribbon-shaped samples.     

How can Mössbauer Spectrometry Contribute to the Characterization of Nanocrystalline Alloys?

A controlled annealing of amorphous precursors represents a simple way of obtaining nanocrystalline alloys featuring interesting magnetic properties suitable for technical applications. They stem from the presence of crystalline nanograins embedded in the amorphous residual matrix which determine the resulting macroscopic parameters. In order to understand correlation between the microstructure and the resulting magnetic behaviour, Mössbauer spectrometry is used as a method of local probe analysis. Possibilities of this technique are discussed and representative examples of investigation of NANOPERM-type nanocrystalline alloys are provided.     

Mössbauer analysis and magnetic properties of Invar Fe–Ni–C and Fe–Ni–Mn–C alloys

The saturation magnetization and the hyperfine magnetic field of different f.c.c. Fe–Ni based alloys containing nearby 29 at .% Ni were studied as a function of temperature and for different Carbon and Manganese contents. We have observed abnormal behaviors that are explained in terms of mixed exchange interactions between atomic spins: J _NiNi(r _i ) < 0, J _FeFe(r _i ) > 0, J _NiFe(r _i ) < 0.     

CoFe2O4纳米颗粒的结构、磁性以及离子迁移

聚乙烯醇(PVA)溶胶凝胶法制备出CoFe₂O₄纳米微粉，用X射线衍射研究了铁氧体纳米颗粒的结构.测量了CoFe₂O₄纳米颗粒80—873 K的变温穆斯堡尔谱，发现纳米颗粒的磁转变温度范围为793—813 K，比块体材料的磁性转变温度要低.CoFe₂O₄纳米颗粒的德拜温度θ_A=674 K，θ_B=243 K，比块体材料要小.CoFe₂O₄纳米颗粒超精细场H_f随温度的变化符合T^3/2+T^5/2定理.当温度较高时，平均同质异能移IS随温度的升高而减小，并呈线性关系. 关键词： 纳米颗粒 磁性 穆斯堡尔谱     

Study of the [Fe(OMe)(dpm)2]2 dimer in the presence of a magnetic field by using Mössbauer spectroscopy

We present a Mössbauer study of a S = 0 ground state magnetic Fe(III)-dimer in the presence of an applied 5 T longitudinal magnetic field, between 7.6 and 33 K. The values obtained for the isomer shift and the quadrupolar splitting are comparable with the ones of Fe(III) ions coordinated to eight oxygen ions. Regarding the spin dynamics, both intramultiplet and intermultiplet transitions are considered. In the chosen temperature range the rate of the former transitions is constant, within the errors, while the rate of the latter ones quickly increases with the temperature.