Slow magnetic order-order transition in the spin chain antiferromagnet Ca3Co2O6

Using powder neutron diffraction, we have discovered an unusual magnetic order-order transition in the Ising spin chain compound Ca3Co2O6. On lowering the temperature, an antiferromagnetic phase with a propagation vector k=(0.5,-0.5,1) emerges from a higher temperature spin density wave structure with k=(0,0,1.01). This transition occurs over an unprecedented time scale of several hours and is never complete.     

First-principles study of electronic structure and magnetic properties of Sr3Fe2O5 oxide

We investigate the electronic structure and magnetic properties of layered compound Sr₃Fe₂O₅ based on first-principles calculations in the framework of density functional theory with GGA+U method. Under high pressure, the ladder-type layered structure of Sr₃Fe₂O₅ is transformed into the infinite layered structure accompanied by a transition from G-type anti-ferromagnetic (AFM) insulator to ferromagnetic (FM) metal and a spin transition from S=2 to S=1. We reproduce these transformations in our calculations and give a clear physical interpretation.     

Investigation of magnetic properties of interacting Fe2O3 nanoparticles

The magnetic properties of Fe₂O₃ nanoparticles (average diameter ∅≅3 nm) in alumina (68% Fe₂O₃ in weight) have been investigated by magnetization measurements. The results indicate a superparamagnetic behavior of interacting particles, which block with decreasing temperature (the zero-field-cooled susceptibility shows a maximum at T≅145 K) with a distribution of relaxation times. A change of magnetic regime is observed below ∼60 K, due to the increasing interparticle interactions and local surface anisotropy.     

Doping effects on the magnetic properties of NdRhIn5 intermetallic antiferromagnet

We report temperature dependent heat capacity and magnetization measurements on single crystals of Nd_1-xLa_xRhIn₅ (x=0.15, 0.4 and 0.5) and NdRhIn_5-xSn_x (x=0.08, 0.12 and 0.24). NdRhIn₅ is an antiferromagnetic (AFM) compound with T_N≈ 11 K which crystallizes in the same layered tetragonal structure of the CeMIn₅ family (M=Rh, Co and Ir), where different ground states can be found by tuning the interplay among different microscopic interactions such as the Kondo effect, crystal field (CEF) effects and the Ruderman-Kittel-Kasuya-Yoshida (RKKY) magnetic interaction. Here, we explore the evolution of the AFM correlations in this Nd-based (non-Kondo) compound while perturbing the RKKY exchange by using two different substitutions: (i) replacing Nd³⁺ by non-magnetic La³⁺ within NdIn₃ atomic planes (dilution) and (ii) substituting In by Sn in the In-sites (electronic tuning). For both types of doping, our results show the suppression of the AFM state as the La- or Sn-content is increased. This doping induced suppression of the AFM order is discussed considering the effects of dilution and effects in the tetragonal CEF using a mean-field model applied to the observed data. Our results are compared to the properties of other members of the RRhIn₅ family considering the role of dimensionality in the magnetic interactions.     

Effect of lanthanum ions on magnetic properties of Y3Fe5O12 nanoparticles

Lanthanum ion (La³⁺)-substituted garnet nanoparticles Y_3?x La _x Fe₅O₁₂ (x = 0.0, 0.2, 0.4, 0.6, 0.8, and 1.0) were fabricated by a sol–gel method. Their crystalline structures and magnetic properties were investigated by using X-ray diffraction (XRD), vibrating sample magnetometer (VSM), and Mössbauer spectrum. The XRD results show that samples of Y_3?x La _x Fe₅O₁₂ (0.0 ≤ x ≤ 0.8) are all single phase and the sizes of particles range from 32 to 65 nm. Those of Y₂LaFe₅O₁₂ consisted of peaks from garnet and LaFeO₃ structures. Compared to pure YIG, the saturation magnetization is larger when the La concentration x = 0.2. However, with increasing La concentration (x), it decreases obviously. Meanwhile, may be due to the enhancement of the surface spin effects, the saturation magnetization rises as the particle size is increased. Different from the pure YIG, the Mössbauer spectra of Y_2.8La_0.2Fe₅O₁₂ and Y_2.2La_0.8Fe₅O₁₂ are composed of four sets of six-line hyperfine patterns. The results tell us that the substitution of La³⁺ ions with large ionic radius (1.061 Å) will give rise to a microscopic structure distortion of the a- and d-sites to different degrees, and the Zeeman sextets from a- and d-sites begin to split into two sub-sextets, which is helpful to explain the phenomenon observed in the study of the magnetic property.     

Magneto-optical properties of the iron garnet Tb3Fe5O12 near the magnetic compensation temperature

The magneto-optical susceptibility and magnetic hysteresis loops of the Faraday effect, which accompany the technical magnetization of the iron garnet Tb₃Fe₅O₁₂, have been investigated experimentally in the temperature region near the magnetic compensation point of this ferrimagnet T _c = 249 K. It has been found that, during the technical magnetization as the temperature approaches the magnetic compensation point T _c , the velocity of domain walls increases, whereas the magneto-optical susceptibility has local maxima to the right and to the left from T _c . Mentioned features of magneto-optical properties of the iron garnet Tb₃Fe₅O₁₂ are associated with the resonance natural frequency of the domain wall oscillations in the crystal with the frequency of the alternating magnetic field. It has been shown that the used theoretical model of the magnetic resonance of domain walls makes it possible to consistently describe (at the qualitative level) the revealed regularities of the variation of the Faraday effect in the iron garnet Tb₃Fe₅O₁₂ near T _c .     

The magnetic cluster blocking in Fe0.35V2O5 spin glass

The Wohlfarth method applied to the semiconducting spin glass Fe_0.35V₂O₅ indicates that the most intensive blocking of magnetic clusters occurs in low magnetic field at 7.5 K just below the temperature of the susceptibility maximum. However, the blocking process is diffused and several classes of clusters are blocked at higher temperatures.     

Critical properties of the models of small magnetic particles of the antiferromagnet MnF2

The static critical behavior of the models of small magnetic particles of the real two-sublattice antiferromagnet MnF₂ is investigated by the Monte Carlo method taking into account the interaction of the second nearest neighbors. Systems with open boundaries are considered to estimate the influence of the sizes of particles on the pattern of their critical behavior. The behavior of thermodynamic functions in the phase transition region is investigated. The data on the maxima of the temperature dependences of heat capacity and magnetic susceptibility are shown to be insufficient to unambiguously determine the effective temperature of the phase transition in the models of small magnetic particles. This requires an additional investigation of the spatial orientation of the sublattice (sublattices) magnetization vector for the models under study.     

混合自旋反铁磁材料Y2BaNiO5的磁学和热力学性质

在格林函数的理论框架下,采用一维自旋为1的各向异性Heisenberg模型来讨论Y2BaNiO5材料的磁学和热力学性质.得到了它的自旋关联函数、低激发谱、基态能(Eg)、比热(C)和静态磁化率(χ)在不同交换各向异性因子下的性质,所得结果与实验和数值模拟结果完全一致.     

Phase diagram and magnetic structures of the two-level singlet antiferromagnet Ho2O2SO4

The orthorhombic holmium oxisulphate orders as a two-sublattice antiferromagnet atT=3.5 K. In external fields along the crystallographica- andc-directions with large and medium-sized magnetic moment, respectively, a ferrimagnetic phase with 1/3 of the saturation magnetization is passed before the paramagnetic phase is reached. Calculations in mean-field theory reveal that for thec-direction the ferrimagnetic phase is not stable atT=0, it only exists for finite temperatures. Magnetization and susceptibility contain large contributions of van Vleck paramagnetism which at any rate have to be taken into consideration. The phase diagram for the two field directions and the magnetic structures of the different phases are established.     

Effect of a SiO2 coating on the magnetic properties of Fe3O4 nanoparticles

In this work the effect of a SiO2 coating on the magnetic properties of Fe3O4 nanoparticles obtained by the sol-gel method is analyzed. Two sets of samples were prepared: Fe3O4 nanoparticles and Fe3O4@SiO2 core-shell composites. The samples display the characteristic spinel structure associated with the magnetite Fe3O4 phase, with the majority of grain sizes around 5-10 nm. At room temperature the nanoparticles show the characteristic superparamagnetic behavior with mean blocking temperatures around 160 and 120 K for Fe3O4 and Fe3O4@SiO2, respectively. The main effect of the SiO2 coating is reflected in the temperature dependence of the high field magnetization (μ(0)H = 6 T), i.e. deviations from the Bloch law at low temperatures (T < 20 K). Such deviations, enhanced by the introduction of the SiO2 coating, are associated with the occurrence of surface spin disordered effects. The induction heating effects (magnetic hyperthermia) are analyzed under the application of an AC magnetic field. Maximum specific absorption rate (SAR) values around 1.5 W g(-1) were achieved for the Fe3O4 nanoparticles. A significant decrease (around 26%) is found in the SAR values of the SiO2 coated nanocomposite. The different heating response is analyzed in terms of the decrease of the effective nanoparticle magnetization in the Fe3O4@SiO2 core-shell composites at room temperature.     

Structural and magnetic properties of CaO-P2O5-SiO2-Fe2O3 glass-ceramics for hyperthermia

Calcium–silica–phosphate glasses containing iron were partially crystallised to obtain a glass-ceramic system, applicable in hyperthermia treatments. The increasing iron content determines a higher glass transition temperature and the disposal of iron ions in small clusters. The magnetisation values for vitroceramic samples suggest that the main contribution to magnetisation is due to iron ions from magnetite.     

Size effect on the structure and magnetic properties of SmMn2O5 nanorods

Three sizes of SmMn₂O₅ nanorods that are labeled with (<L_C>) × axial lengths of 58(17) nm × 25(6) nm, 92(21) nm × 32(8) nm, and 126(25) nm × 52(13) nm were fabricated by the hydrothermal method. All the samples exhibited an antiferroicmagnetic (AFM) peak at approximately 6 K, which was associated with Sm magnetic ordering and no size independence. Another AFM magnetic ordering that belongs to the Mn ion was found with <L_C> = 58 nm, 92 nm, and 126 nm at 26 K, 28 K, and 30 K, respectively. The spin-orbit interaction increases with size in the magnetic susceptibility experiment. All the samples displayed a hysteresis loop at 2 K. The coercivity decreases as the size increases. The effects of the size on the crystal structure were elucidated from the Raman spectra of the <L_C> = 92 and 126 nm samples at various temperatures. The 126 nm sample displayed a red-shift for the Ag mode with warming, revealing that the Mn–O bonds are more sensitive to temperature in larger SmMn₂O₅ nanorods. These results demonstrate that the size effect importantly affects the structure and magnetic properties in SmMn₂O₅ multiferroic nanorods.     

Nuclear magnetic resonance in noncollinear antiferromagnet Mn3Al2Ge3O12

The ⁵⁵Mn nuclear magnetic resonance spectrum of noncollinear 12-sublattice antiferromagnet Mn₃Al₂Ge₃O₁₂ has been studied in the frequency range of 200–640 MHz in the external magnetic field H ‖ [001] at T = 1.2 K. Three absorption lines have been observed in fields less than the field of the reorientation transition H _c at the polarization h ‖ H of the rf field. Two lines have been observed at H > H _c and h ⊥ H. The spectral parameters indicate that the magnetic structure of manganese garnet differs slightly from the exchange triangular 120-degree structure. The anisotropy of the spin reduction and (or) weak antiferromagnetism that are allowed by the crystal symmetry lead to the difference of ≈3% in the magnetization of sublattices in the field H < H _c. When the spin plane rotates from the orientation perpendicular to the C ₃ axis to the orientation perpendicular to the C ₄ axis, all magnetic moments of the electronic subsystem decrease by ≈2% from the average value in the zero field.     

Effect of doping on the magnetic properties of the low-dimensional antiferromagnet CuO

The effect of doping with Li⁺, Zn²⁺, Ni²⁺, and Ga³⁺ ions on the magnetic susceptibility of the low-dimensional antiferromagnet CuO (T _N=230 K) has been studied within a broad temperature range of 77–600 K. The solubility of impurity ions in the CuO lattice is low, ⩽3%. Impurity ions, similar to intrinsic defects, distort antiferromagnetic coupling and can shift the long-and short-range magnetic-order regions toward lower T. Fiz. Tverd. Tela (St. Petersburg) 40, 1876–1880 (October 1998)     

Spin-order and magnetic properties of BaZn2Fe16O27 (Zn2-W) hexagonal ferrite

We have observed large peaks in the ultrasonic attenuation of a pure and two doped LaAl₂ crystals in the temperature region of about 45 K which are possibly of the Bordoni type. Their most interesting characteristics are:

1. There is only one peak in each sample.
2. The peaks are so narrow that they can be described by the original Seeger model with only one actication energy and one attempt frequency.