Micro-structures of an amorphous alloy (Cu57Hf43) detected by tdpac measurements

TDPAC spectra of¹⁸¹Hf were measured for an amorphous alloy (Cu₅₇Hf₄₃) prepared by meltspinning for the first time. It is obtained that two Hf sites exist in the amorphous alloy. The short-range order in the amorphous alloy is discussed from a viewpoint of the polytope model of amorphous solids.     

Variation of magnetic state of amorphous Fe90Zr10 and Fe91Hf9 by the charge of hydrogen

Amorphous Fe₉₀Zr₁₀ and Fe₉₁Hf₉ ribbons were charged with hydrogen by the electrochemical method up to Fe₉₀Zr₁₀H₂₆ and Fe₉₁Hf₉H₁₅, respectively, and the change in magnetic structures were analyzed by Mössbauer spectrometry. The internal magnetic field appeared by the charge of hydrogen, the degree of change being depended on amounts of hydrogen included in amorphous Fe₉₀Zr₁₀ and Fe₉₁Hf₉, although Fe₉₁Hf₉ absorbed hydrogen more slowly than Fe₉₀Zr₁₀. The differences of hydrogen inclusion and Mössbauer hyperfine structure between Fe₉₀Zr₁₀ and Fe₉₁Hf₉ were discussed based on the results of a hyperfine field distribution and the radial distribution functions of Fe?Fe obtained by EXAFS.     

Ferromagnetic-to-antiferromagnetic transition in (Hf1−xTix)Fe2 intermetallic compounds induced by geometrical frustration of the Fe(2a) sites

The ferromagnetic-to-antiferromagnetic transition in the hexagonal (Hf_1−xTi_x)Fe₂ (0?x?1) intermetallic compounds has been investigated by ⁵⁷Fe Mössbauer spectroscopy. At 10 K, the transition occurs within rather narrow concentration limits, around x=0.55–0.65. We found that the key factor governing the unexpected quick change of the magnetic structure is the magnetic frustration of the Fe(2a) sites. The magnetic frustration is caused by the noncollinearity of the Fe(6h) magnetic sublattice. The noncollinearity arises from the rotation of the magnetic moments due to the competition between the ferromagnetic exchange interactions and the antiferromagnetic Fe(6h)–Ti–Fe(6h) interaction. In the compounds with x=0.4–0.6, the temperature transitions to the antiferromagnetic state are observed. As an example, the Hf_0.4Ti_0.6Fe₂ compound is completely antiferromagnetic above 200 K.     

Measurements of the hyperfine magnetic fields at Ta and Fe in the Laves compounds (Zrx Hf1−x)Fe2 for 0≤x≤1

The hyperfine magnetic fields at¹⁸¹Ta and⁵⁷Fe in the ferromagnetic Laves intermetallic compounds (Zr_xHf_1?x)Fe₂ (0≤x≤1) have been measured by the methods of TDPAC and Mössbauer effect, respectively, and shown to be practically independent of x at x≥0.4. An average value B_hf (Ta)=?6.52 T at 300 K was obtained for samples with x≥0.4, and ?14.2 T for pure HfFe₂ in the hexagonal C14 modification. For 0hf(Ta) in (Zr_0.9 Hf_0.1)Fe₂ from that for B_hf (Fe) and the bulk magnetization was confirmed, studied in detail, and shown to exist for all x≥0.4. The temperature dependence of B_hf(Ta) in HfFe₂ was close to that of B_hf (Fe).     

Transverse spin freezing in Fe92.5Hf7.5

Amorphous Fe_92.5Hf_7.5 has been studied by Mössbauer spectroscopy and magnetization measurements. Transverse spin freezing has been observed at 47 ± 8 K, and the results are compared with those for amorphous iron-rich Fe-Zr alloys in which transverse spin freezing is also observed.     

Mössbauer study of amorphous Fe2RE (RE=Ce,Er) alloys

Among amorphous Fe₂RE (RE=Er, Ce, Gd, La, Pr, Sm, Dy, Ho) alloys, Fe₂Ce exhibits a tendency toward short range order, while the other Fe₂RE compounds show clustering. However, we have almost no information about environments around Fe atoms. Using Mössbauer spectroscopy we have determined the quadrupole splitting distributionsP(QS) of two representative amorphous Fe₂RE (RE=Ce, Er) alloys, leading to local environments of Fe atoms. The analysis of the mixed magnetic dipole and quadrupole interactions in Fe₂Er shows two kinds of electrical field gradients (EFT) with the positive and negative signs in the sample, indicating a random packing of Fe atoms. Furthermore, the analyzed quadrupole splitting distributionP(QS) of Fe₂Er also supports random packing in this amorphous alloy. On the other hand, the amorphous Fe₂Ce alloy shows two kinds of distributions of quadrupole splitting; the major component indicating random packing and the minor component Ce-rich Ce-Fe clusters.     

Microstructure and some magnetic properties of bulk amorphous (Fe0.61Co0.10Zr0.025Hf0.025Ti0.02W0.02B0.20)100−xYx (x=0, 2, 3 or 4) alloys

Microstructure, revealed by X-ray diffraction, transmission electron microscopy and Mössbauer spectroscopy, and magnetic properties such as magnetic susceptibility, its disaccommodation, core losses and approach to magnetic saturation in bulk amorphous (Fe_0.61Co_0.10Zr_0.025Hf_0.025Ti_0.02W_0.02B_0.20)_100−xY_x (x=0, 2, 3 or 4) alloys in the as-cast state and after the annealing in vacuum at 720 K for 15 min. are studied. The investigated alloys are ferromagnetic at room temperature. The average hyperfine field induction decreases with Y concentration. Due to annealing out of free volumes its value increases after the heat treatment of the samples. The magnetic susceptibility and core losses point out that the best thermal stability by the amorphous (Fe_0.61Co_0.10Zr_0.025Hf_0.025Ti_0.02W_0.02B_0.20)₉₇Y₃ alloy is exhibited. Moreover, from Mössbauer spectroscopy investigations it is shown that the mentioned above alloy is the most homogeneous. The atom packing density increases with Y concentration, which is proved by the magnetic susceptibility disaccommodation and approach to magnetic saturation studies.     

退火处理Fe43Co43Hf7B6Cu1非晶合金的正电子湮没研究

对熔体急冷法制备的Fe₄₃Co₄₃Hf₇B₆Cu₁非晶合金进行了200,300,400和500 ℃保温30 min的退火处理,用正电子湮没寿命谱、X射线衍射、穆斯堡尔谱等方法研究了退火后试样的结构及结构缺陷变化.结果表明,在非晶合金的制备态,正电子主要在非晶基体相空位尺寸的自由体积中湮没,湮没寿命τ₁为158.4 ps,强度I₁关键词： 43Co₄₃Hf₇B₆Cu₁非晶')" href="#">Fe₄₃Co₄₃Hf₇B₆Cu₁非晶 退火处理 正电子湮没寿命 结构与结构缺陷     

Mössbauer spectroscopy of creep-annealed soft magnetic amorphous alloys

To produce magnetic anisotropy in amorphous alloys, stress-annealing above the Curie temperature was substituted for the common thermomagnetic treatment. A tilting three-angle Mössbauer method was applied to see the changes of the⁵⁷Fe hyperfine field directions and intensities due to this procedure. The resulting pictures of the domain orientations distribution in the Fe₈₀Cr₂B₁₄Si₄ and Fe₄₀Ni₄₀B₂₀ amorphous alloys are compared with the measured magnetic anisotropies and domain structures.     

Temperature dependence of the hyperfine field in amorphous Fe2O3

Mössbauer spectroscopy was used to follow the hyperfine field at ⁵⁷Fe nuclei in amorphous Fe₂O₃. The value of H_hf at T = 0, 470 kG, indicates $\text{J}\text{=}\text{5}\text{2}$ for the Fe ions, while the reduced hyperfine field versus reduced temperature closely follows a $\text{J}\text{=}\text{1}\text{2}$ Brillouin function. This result is at variance with theoretical predictions for a spin glass and is also different from amorphous metals with a high content of magnetic ions as reported in the literature. Paramagnetic Mössbauer spectra of amorphous mixed oxides of Fe₂O₃ with ZnO and CoO show that the ⁵⁷Fe nuclei in all amorphous ferric oxides studied so far are coordinated in a manner similar to the d site in β F₂O₃, and distinctly different from the coordination in their crystalline form.     

Influence of milling time on the structural, microstructural and magnetic properties of mechanically alloyed Ni58Fe12Zr10Hf10B10 nanostructured/amorphous powders

This paper investigates structural, microstructural and magnetic properties of amorphous/nanocrystalline Ni₅₈Fe₁₂Zr₁₀Hf₁₀B₁₀ powders prepared by high energy milling. Ball milling of Ni, Fe, Zr, Hf and B leads to alloying of the element powders at 120 h. The results show that at 190 h the amorphous content is at the highest level and the grain size is about 2 nm. The magnetic measurements reveal that the coercivity and the saturation magnetization reach about 20 Oe and 30 emu/g at 190 h and become approximately 5 Oe and 40 emu/g after a suitable heat treatment, respectively.     

Short-Range Order in Amorphous and Crystalline Ferroelectric Hf<Subscript>0.5</Subscript>Zr<Subscript>0.5</Subscript>O<Subscript>2</Subscript>

The microstructures of amorphous and polycrystalline ferroelectric Hf_0.5Zr_0.5O₂ films are studied by X-ray spectroscopy and ellipsometry. EXAFS spectra demonstrate that the amorphous film consists of an “incompletely mixed” solid solution of metallic oxides HfO₂ and ZrO₂. After rapid thermal annealing, the mixed Hf_0.5Zr_0.5O₂ oxide films have a more ordered polycrystalline structure, and individual Hf and Zr monoxide islands are formed in the films. These islands are several nanometers in size and have a structure that is similar to the monoclinic structure of HfO₂ and ZrO₂. The presence of the HfO₂ and ZrO₂ phases in the Hf_0.5Zr_0.5O₂ films is also detected by ellipsometry.     

Soft magnetic properties of amorphous Fe52Co34Hf7B6Cu1 alloy treated by pulsed magnetic field and annealing

<正>The crystallization,microstructure,and soft magnetic properties of Fe₅₂Co₃₄Hf₇B₆Cu₁ alloy are studied.Amorphous Fe₅₂Co₃₄Hf₇B₆Cu₁ alloys are first treated by a pulsed magnetic field with a medium frequency,and then annealed at 100℃-400℃for 30 min in a vacuum.The rise in temperature during the treatment by a pulsed magnetic field is measured by a non-contact infrared thermometer.The soft magnetic properties of specimens are measured by a vibrating sample magnetometer（VSM）.The microstructure changes of specimens are observed by a Mossbauer spectroscopy and transmission electron microscope（TEM）.The results show the medium-frequency pulsating magnetic field will promote nanocrystallization of the amorphous alloy with a lower temperature rise.The nanocrystalline phase isα-Fe（Co） with bcc crystal structure,and the grain size is about 10 nm.After vacuum annealing at 100℃for 30 min,scattering nanocrystalline phases become more uniform,the coercive force and the saturation magnetization of the specimens are 41.98 A/m and 185.15 emu/g.     

Magnetic properties of nanocrystalline composite in the Nd--Fe--B system

Using ⁵⁷Fe Mössbauer spectroscopy, X-ray diffraction and magnetization measurements, magnetic properties of melt-spun Nd_4.5Fe₇₇B_18.5 ribbon have been investigated after the annealing treatments which make nanocrystalline composite from the as-prepared amorphous state. Specimen ribbon which shows coercivity and is suitable for a permanent magnet consists of the mixture of Fe₃B and Nd₂Fe₁₄B. Relative fraction of these phases in the ribbon have been determined.     

Mössbauer effect study of R2Fe14C (R=Dy and Er) compounds

The results of⁵⁷Fe Mössbauer effect measurements and magnetic studies performed on Dy₂Fe₁₄C and Er₂Fe₁₄C compounds are reported. The magnetic contributions of different iron sites are estimated and compared with those of corresponding boron compounds. The magnetic behaviour of the studied compounds is analysed in the molecular field approximation considering a two sublattices ferrimagnet.     

Vibrational dynamics of Fe in amorphous Fe–Sc and Fe–Al alloy thin films

The atomic vibrational dynamics of ⁵⁷Fe in 800-Å thick amorphous (a-) ⁵⁷Fe_0.25Sc_0.75, a-⁵⁷Fe_0.67Sc_0.33 and a-⁵⁷Fe_0.14Al_0.86 alloy thin films has been investigated at room temperature by nuclear resonant inelastic X-ray scattering (NRIXS) of synchrotron radiation. The amorphous phase has been successfully stabilized by codeposition of Fe and Sc or Al in ultrahigh vacuum onto substrates held at –140 °C during deposition. The amorphous structure of the samples was confirmed by X-ray diffraction and conversion electron Mössbauer spectroscopy. The ⁵⁷Fe-projected partial vibrational density of states, g(E), has been obtained from the measured NRIXS vibrational excitation probability, together with thermodynamic quantities such as the probability of recoilless absorption (f-factor), the average kinetic energy per Fe atom, the average force constant, and the vibrational entropy per Fe atom. A plot of the reduced density of states, g(E)/E², versus excitation energy E proves the existence of non-Debye-like vibrational modes (boson peak) with a peak energy, E _bp , in the range of 3–7 meV. Both, the boson peak height H _bp and E _bp were found to depend on the composition. Above the boson peak, g(E)/E² exhibits an exponential decrease. Our results demonstrates that the features of the boson peak depend on the amount and type of element M (M = Al, Si, Mg, Sc).     

Magnetic insulator glasses

An outline is given of the use of Mössbauer spectroscopy as a probe of the amorphous structure and magnetic coordination in magnetic insulator glasses. Using the⁵⁷Fe Mössbauer resonance as an example in the context of amorphous ferric oxides and fluorides, the manner in which both paramagnetic and hyperfine-field-split spectra can be analyzed is presented. Emphasis is given to the information contained in Mössbauer lineshapes and linewidths in addition to the more obvious line-position data. A number of general findings are set out for ferric speromagnetics with particular references to Mössbauer studies of amorphous Fe₂O₃, Y₃Fe₅O₁₂ (YIG), FeF₃ and NaFeF₄.     

Mössbauer Study of the Fe3B/Nd2Fe14B Nanocomposite Magnet by the Addition of Co

The addition of Co to Nd₄Fe_77.5–x Co _x Hf_0.5Ga_0.5B_18.5 (0x5) was found to enhance the magnetic properties of Fe₃B/Nd₂Fe₁₄B nanocomposite magnets. The enhancement resulted from the fact that Co tends to retard the formation of Fe₃B from the amorphous matrix but to accelerate that of Nd₂Fe₁₄B. The decreased interval between the crystallization temperature of Fe₃B and Nd₂Fe₁₄B led to a uniform grain size distribution of both phases during the annealing treatment. The additive Co was confirmed to partition mainly to Nd₂Fe₁₄B crystals rather than to Fe₃B which was traced by XRD and Mössbauer spectroscopy as well. About 72 vol.% of Fe₃B, 27 vol.% of Nd₂Fe₁₄B, and a small amount of Fe around 1 vol.%, respectively, were found to form. However, the volume fraction of each phase did not vary by the addition of Co up to 5 at.%.     

Distribution of hyperfine fields of57Fe2+ in amorphous LiNbO3: Mössbauer study at low temperatures in high magnetic fields

Mössbauer spectra of amorphous LiNbO₃ doped with⁵⁷Fe²⁺ ions were measured atT≥4.2 K in external magnetic fields up toH=5.5 T. It was found that the oxygen octahedra around the high-spin Fe²⁺ ions are randomly distorted obeying no symmetry at all. The correlation of isomer shift and quadrupole splitting is probably due to T_2g distortions.     

Local structure of Fe70Cr15B15 X-ray amorphous alloy

The local atomic and magnetic structure of Fe₇₀Cr₁₅B₁₅ X-ray amorphous alloy is studied by means of ¹¹B nuclear magnetic resonance (NMR) and ⁵⁷Fe Mössbauer spectroscopy. It is determined that Fe₈₅B₁₅ and Fe₇₀Cr₁₅B₁₅ X-ray amorphous alloys consist of microregions (nanocrystals) with short-range orders of t-Fe₃B and α-Fe phases. It was found out that chromium atoms in the Fe₇₀Cr₁₅B₁₅ X-ray amorphous alloy are evenly distributed in these two nanocrystals, forming t-(Fe,Cr)₃B and α-Fe(Cr) phases.