Das kritische magnetische Verhalten von EuO

Mössbauer effect and magnetization measurements were employed in order to study the static and especially the dynamic magnetic properties of the nearly Heisenberg ferromagnet EuO near its Curie temperature,T _c=69.2 °K. The critical exponent β of the spontaneous magnetization was determined to be β=0.34±0.02. It was shown that critical slowing down of spin fluctuations takes place nearT _c with spin relaxation times between 7×10^?11 sec (T=1.01T _c) and 1.5×10^?1 sec (T=1.03T _c). The experimental values of the relaxation time were found to be in satisfactory agreement with theoretically computed ones. Just belowT _c the Mössbauer spectra exhibit relaxation effects, which are characteristic for the occurence of critical super-paramagnetism. Investigations of several samples indicated quantitatively, that critical superparamagnetism has its origin in the non ideal composition of the real crystal.     

Influence of zeolite water on paramagnetic and ferromagnetic resonances in the Co2[Nb(CN)8] · 8H2O molecular magnet

The contributions of Co²⁺ and Nb⁴⁺ ions to the high-frequency dynamic magnetic susceptibility of the Co₂[Nb(CN)₈] · 8H₂O molecular magnet in the paramagnetic state at T > 12 K are separated. It is found that the ferromagnetic ordering, which leads to the reconstruction of the electron paramagnetic resonance spectrum into the ferromagnetic resonance spectrum, occurs at T < 12 K. The influence of zeolite water on the spectra of the paramagnetic and ferromagnetic resonances is found. Dehydration leads to a decrease in the time of the spin relaxation of the ferromagnetic system from 50 ps to 17 ps at T = 4 K and to the variation in the temperature dependences of the widths of the lines and g factors in the electron spin resonance spectra.     

Spin gap, phase separation and d-wave pairing as revealed by electron spin-lattice relaxation in 123 and 124 YBaCuO systems doped with Gd3+

With an original modulation technique, the Gd³⁺ electron spin-lattice relaxation has been investigated in normal and superconducting states of YBa₂Cu₃O_6+x (123) and YBa₂Cu₄O₈ (124) compounds doped with 1% Gd. In the 123 sample withx = 0.9T _c = 90 K), theT ₁ behavior within 50 <T< 200 K reveals the [1 ? tanh²(Δ/2kT)]/T dependence typical of a spin gap opening with Δ ≈ 240 K. Below 50 K, the exponential slowing down ofT ₁ is limited by the Korringa-like behaviorT ₁ T = const); the same Korringa-like law is found in the 123 sample withx = 0.59 (T _c = 56 K) within the total 4.2–200 K temperature range. This is interpreted in terms of microscopic separation of the normal and superconducting phases allowing for the electron spin cross-relaxation between them. In the 124 sample (T _c = 82 K), the Gd³⁺ relaxation rate below 60 K is found to obey a power lawT _n with an exponentn ≈ 3. Such a behavior (previously reported for nuclear spin relaxation) is indicative of the d-wave superconducting pairing. Additional paramagnetic centers characterized by relatively slow spin-lattice relaxation are found in both 123 and 124 systems. A well-pronounced change in theT ₁ temperature dependence atTT* ≈ 180–200 K is observed for these slowly relaxing centers as well as for the conventional, fast-relaxing Gd³⁺ ions, suggesting microscopic phase separation and a change in the relaxation mechanism due to electronic crossover related with the opening of the spin gap. This hypothesis is supported by some “180 K anomalies” previously reported by other authors.     

Electron spin resonance analysis of magnetic structures in La2/3Ca1/3MnO3

Measurements of electron spin resonance (ESR) of La_2/3Ca_1/3MnO₃ (LCMO) in the ferromagnetic and paramagnetic phases were carried out. Phase transition and temperature dependence of the peak-to-peak ESR linewidth were determined. The transition temperature between ferromagnetic and paramagnetic phases was observed at 265 K. A prominent increase of the peak-to-peak linewidth with decreasing temperature below T_c was observed. Using the dynamic scale theory and block spin transformation in critical phenomenon, the quantitative calculation of peak-to-peak linewidth at near T_c was made, which was in good agreement with the experimental data. It was believed that the long interactions between the ferromagnetic microregions for LCMO played a key role in determining the ESR linewidth.     

NMR studies of magnetic properties in Heusler-type Mn 3 Si

In order to microscopically investigate the magnetic properties of both paramagnetic and antiferromagnetic phases in Mn₃Si (T _N?=?23 K), the ⁵⁵Mn NMR has been carried out at temperatures between 2.2 K and 300 K. The temperature dependences of the spectrum, Knight shift (or resonance frequency shift) and spin-lattice relaxation time T ₁ of ⁵⁵Mn NMR have been measured. In the paramagnetic phase, only one resonance spectrum can be obtained. The observed spectrum is identified to be a signal corresponding to the Mn(II) site. In the antiferromagnetic phase, two different spectra corresponding to the Mn(I) and Mn(II) sites are found at the resonance frequencies of 145 and 6 MHz, respectively, by the zero field NMR at 4.2 K. From these results, the internal magnetic fields on the ⁵⁵Mn(I) and ⁵⁵Mn(II) nuclei are found to be 13.6 and 0.6 T, respectively. According to the NMR results, the helical structure in incommensurate Mn spin states is better explained compared with the transverse sinusoidal structure.     

Heat capacity of a five-coordinated ferromagnet,chloro bis(N,N-diethyldithiocarbamato)iron(III), in the temperature range from 0.4 to 20 K

The heat capacity of polycrystalline Fe[S₂CN(C₂H₅)₂]₂Cl has been measured in the temperature range from 0.411 to 19.55 K. The transition between ferromagnetic and paramagnetic states is characterized by a sharp λ-type anomaly centered at the Curie temperature, T_c = 2.412 ± 0.008 K. The enthalpy and the entropy of transition are 40.475 J mol^?1 and 11.199 J K^?1mol^?1 (= 1.347 R), respectively. The transition entropy is only 2.81% smaller than R In 4. This fact ascertains that the spin manifold is really a quartet. The ground spin states of the present compound are characterized by a zero-field splitting of the $\text{S =}\text{3}\text{2}$ state into two Kramers' doublets. The overlapping non-cooperative Schottky-type anomaly due to the energy separation between the two Kramers' doublets is separated tentatively from the cooperative heat capacity due to the exchange interaction. Based on a careful analysis of the transition entropy it may be concluded that the magnetic structure of the present complex would be a two-dimensional triangular Ising lattice. The exchange and the Curie-Weiss constants are also determined to be 0.155 and 4.19 K, respectively.     

Valence and magnetic states of impurity iron ions in the La<Subscript>0.75</Subscript>Sr<Subscript>0.25</Subscript>Co<Subscript>0.98</Subscript>Fe<Subscript>0.02</Subscript>O<Subscript>3</Subscript> perovskite

The local magnetic and valence states of impurity iron ions in the rhombohedral La_0.75Sr_0.25Co_0.98 ⁵⁷Fe_0.02O₃ perovskite were studied using Mössbauer spectroscopy in the temperature range 87–293 K. The Mössbauer spectra are described by a single doublet at 215–293 K. The spectra contained a paramagnetic and a ferromagnetic component at 180–212 K and only a broad ferromagnetic sextet at T < 180 K. The results of the studies showed that, over the temperature range 87–295 K, the iron ions are in a single (tetrahedral) state with a valence of +3. In the temperature range 180–212 K, two magnetic states of Fe³⁺ ions were observed, one of which is in magnetically ordered microregions and the other, in paramagnetic microregions; these states are due to atomic heterogeneity. In the magnetically ordered microregions in the temperature range 87–212 K, the magnetic state of the iron ions is described well by a single state with an average spin S = 1.4 ± 0.2 and a magnetic moment μ(Fe) = 2.6 ± 0.4μ _B .     

Dielectric relaxation and magnetic characteristics of the Bi0.5La0.5MnO3 ceramics

The complex permittivity ?* of ceramics of bismuth-lanthanum manganite Bi_0.5La_0.5MnO₃ has been measured in ranges of temperatures T = 10–200 K and frequencies f = 10²–10⁶ Hz. Clearly pronounced regions of the non-Debye dielectric relaxation have been revealed at low temperatures (T < 90 K). To describe them, the possible mechanisms have been proposed and discussed. The temperature dependences of magnetization, the anomalous behavior of which can be associated with the phase transition from the paramagnetic phase into the ferromagnetic phase occurring at T ～ 40–80 K, have been measured in the temperature range T = 10–120 K.     

Electron spin resonance and longitudinal relaxation around phase transition in La0.9Ca0.1 MnO3

With original modulation technique, the longitudinal electron spin-relaxation timeT ₁ has been measured in the La_1-xCa_xMnO₃ manganite (x = 0.1) both in the paramagnetic state and around the temperature (T _c) of the ferromagnetic ordering. The data are compared with the evolution of the transverse relaxation time T₂ as determined from the electron spin resonance (ESR) linewidth. Well above T_c, theT ₁ =T ₂ equality was confirmed, whereas a steep slowing down ofT ₂ was observed asT _c was approached (theT ₁/T₂ ratio increased by two orders of magnitude). The temperature dependence ofT ₁ within the whole temperature range was found to be consistent with that ofT · χ(T), where χ(T) is the electron-spin susceptibility obtained from the ESR absorption area. The interpretation suggests that both the longitudinal and transverse electron-spin relaxation rates are governed by strong exchange interaction between the Mn ions, the ESR linewidth being inhomogeneously broadened in the vicinity of the phase transition.     

Relaxation mechanism in γ-ray-irradiated L-alanine studied by transfer saturation EPR and pulse EPR

Stable paramagnetic centers in γ-ray-irradiated L-alanine dosimeters exhibit a maximum in relaxation rate in the vicinity of 190 K. The mechanism of this relaxation rate has been investigated on the first stable alanine radical center, SARI, by employing continuous-wave transfer saturation electron paramagnetic resonance and pulse electron paramagnetic resonance techniques. The detected in-phase and out-of-phase spectra as well as phase memory times,T _M, indicate that besides the well-known τ_p of the CH₃ group of SAR1 an additional correlation time, τ_l (ΔElk=2689±50 K and 0 τ₁₀ = 0.15 ± 0.03 ps), is involved in the transverse relaxation process and effects the SAR1 center. For the SAR1 center this mechanism originates from the hindered motion of undamaged CH₃ and NH ₃ ⁺ groups in the lattice. The motion of these groups additionally effects the spectrum of the SAR1 center through averaging out of the anisotropic splitting.     

Anomalous magnetism and 209Bi nuclear spin relaxation in Bi4Ge3O12 crystals

The quadrupole ²⁰⁹Bi spin–spin and spin–lattice relaxation were studied within 4.2–300 K for pure and doped Bi₄Ge₃O₁₂ single crystals which exhibit, as was previously found, anomalous magnetic properties. The results revealed an unexpectedly strong influence of minor amounts of paramagnetic dopants (0.015–0.5 mol.%) on the relaxation processes. Various mechanisms (quadrupole, crystal electric field, electron spin fluctuations) govern the spin–lattice relaxation time T ₁ in pure and doped samples. Unlike T ₁, the spin–spin relaxation time T ₂ for pure and Nd-doped samples was weakly dependent on temperature within 4.2–300 K. Doping Bi₄Ge₃O₁₂ with paramagnetic atoms strongly elongated T ₂. The elongation, although not so strong, was also observed for pure and doped crystals under the influence of weak (～30 Oe) external magnetic fields. To confirm the conclusion about strong influence of crystal field effects on the temperature dependence of T ₁ in the temperature range 4.2–77 K, the magnetization vs. temperature and magnetic field was measured for Nd- and Gd-doped Bi₄Ge₃O₁₂ crystals using a SQUID magnetometer. The temperature behavior of magnetic susceptibility for the Nd-doped crystal was consistent with the presence of the crystal electric field effects. For the Gd-doped crystal, the Brillouin formula perfectly fitted the curve of magnetization vs. magnetic field, which pointed to the absence of the crystal electric field contribution into the spin–lattice relaxation process in this sample.     

Pulsed EPR hole-burning experiment on dangling bond centers in a-Si:H aerosol particles formed by thermal decomposition of silane

Si dangling bond centers in aerosol particles of amorphous hydrogenated silicon formed by thermal decomposition of SiH₄ in Ar were studied by pulsed electron paramagnetic resonance. The hole-burning and inversion-recovery experiments demonstrate that large-scale rapid spectral diffusion takes place in the samples with high spin concentration. Correlation times τ_c of the spectral diffusion and spin-lattice relaxation timesT ₁ were obtained in the temperature range between 77 and 290 K. Above 130 K, τ_c andT ₁ are proportional one to the other. The unusual feature of this spectral diffusion is that the shape of the central part of the spectral hole does not change when the delay time increases. The other paramagnetic centers previously investigated showed a remarkable change of the hole shape which was induced by modulation of dipolar interaction due to spin flips. It is suggested that the observed anomaly in the Si dangling bond centers arises due to cooperative spin flips.     

NMR investigations of dynamical processes in orientationally ordered and disordered NaCN,RbCN and CsCN

The nuclear spin lattice relaxation timeT ₁ of the²³Na,⁸⁵Rb,⁸⁷Rb,¹³³Cs,¹⁴N nuclei is measured in NaCN, RbCN and CsCN as a function of temperature below and above the ferroelastic phase transition temperatureT _c. BelowT _c the behaviour ofT ₁ of the alkali nuclei renders possible to determine the flip frequency of the CN molecules and its temperature dependence. AboveT _c from the¹⁴NT ₁ the correlation time τ_c of the rotational motions of the CN molecules and its temperature dependence is determined. An empirical rule is verified demonstrating that atT _c the correlation times take nearly the same values for all cyanides. For the high and low temperature phases one obtains atT _c about τ_c=5·10^?13s and τ_c=5·10^?11s, respectively. The results are discussed with respect to the mechanism of the phase transition.     

Pulsed NMRON measurements on insulators

Selective single and double quantum excitation pulsed NMRON has been utilized to obtain rotation patterns, free induction decays, and spin echoes in antiferromagnetic⁵⁴Mn−MnCl₂·4H₂O and the quasi-2 dimensional ferromagnet⁵⁴Mn−Mn(COOCH₃)₂·4H₂O. The pulsed technique is well suited to observing fast spin-lattice relaxation and T₁ values down to 100 ms have been measured in these systems. These short times may make magnetic insulators viable hosts for on-line experiments. The dependence on field and temperature of the⁵⁴Mn spin-lattice relaxation time T₁ has been investigated and a T₁ minimum at high fields observed in both systems. A spin-spin relaxation time T₂≈50 μs is measured in⁵⁴Mn−MnCl₂·4H₂O. The observation of NMRON in the paramagnetic phase of MnCl₂·4H₂O allows the resonant frequencies in the antiferromagnetic and paramagnetic phases to be compared, yielding a value for the zero point spin deviation in the former phase.     

非晶态Fe13Ni67.2P4.5B15.3合金的临界现象

本文报道非晶态Fe₁₃Ni_67.2P_4.5B_15.3合金的磁化强度与温度和磁场关系的测量结果。在居里温度附近样品的磁特性符合二级相变规律,得到临界指数β=0.39±0.02,γ=1.56±0.06,δ=5.20±0.1,样品的居里温度T_c=(180.4±0.2)K。在实验误差范围内,临界指数β,γ,δ满足γ=β(δ-1)关系,在168—192K温度范围,实验数据满足二级相变的磁状态方程。当T>270K时,样品顺磁磁化率服从居里-外斯定律,由居里-外斯常数c计算出有效顺磁磁矩P_eff=3.19 μ_B。 关键词：     

Static and dynamic behavior of the cluster phase in LaMn0.6Co0.4O3

A non-uniform magnetic state in the perovskite system LaMn_0.6Co_0.4O₃ has been studied by magnetometric methods. Two ferromagnetic (FM) critical temperatures are observed. The first one at T_C1≈217 K is ascribed to the onset of FM state in the Mn⁴⁺/Co²⁺-ordered domains (phase 1), while the disordered regions containing Mn⁴⁺, Mn³⁺, Co³⁺ and Co²⁺ valence states (phase 2) remain in the paramagnetic state. Below T_C2≈147 K a long-range FM arrangement develops also in certain part of phase 2, but the major part of phase 2 is formed by polydisperse FM clusters. This second transition is accompanied by a huge increase of coercivity and by occurrence of long-time relaxation. Finally, between 40 and 65 K, a frequency-dependent maximum in the imaginary part of the ac susceptibility is observed, which can be ascribed to the relaxation of small clusters behaving superparamagnetically.     

ESR study of magnetic structures in La0.7Ca0.3MnO3

Comprehensive measurements of electron spin resonance (ESR) and magnetization of La_0.7Ca_0.3MnO₃ in the ferromagnetic as well as paramagnetic phases were carried out. Quantitative evidences for the inhomogeneous magnetic structure, consisting of ferromagnetic microregions embedded in the antiferromagnetic surrounding near T_c, were found. It is suggested that the microscopic local magnetic structures above and below T_c are qualitatively similar except that the phase below T_c carries long range order between the ferromagnetic microregions whose sizes grow with decreasing temperature.     

Electron spin-lattice relaxation in noncommon metals YBa2Cu3Ox and Rb1C60

Using an original modulation technique, the electron spin-lattice relaxation have been investigated in two noncommon metals: YBa₂Cu₃O_x, high-T_c material doped with 1% Gd, and Rb₁C₆₀, linear polymer phase fulleride. In the first case, the Korringa-like temperature dependence of the Gd³⁺ longitudinal relaxation time T₁, is found forx = 6.59 in a wide temperature range 4.2 <T < 200 K, both above and below T_c = 56 K. Atx = 6.95 (T_c = 90 K), the T₁ behavior within 50 <T < 200 K is evidently affected by spin gap opening with the gap value of about 240 K. At 200 K, an unexpected acceleration of the relaxation rate takes place, suggesting some change in the relaxation mechanism. The data are discussed in terms of the Barnes-Plefke theory with allowance made for microscopic separation of the normal and superconducting phases. In Rb₁C₆₀, the evolution of the ESR line and relaxation rates have been studied accurately in the range of the metal-insulator transition (below 50 K). Interpretation is suggested which takes into account breaking down the relaxation bottleneck due to opening of the energy gap near the Fermi surface. The gap value of about 100 cm^?1 is estimated from the analysis of relaxation rates, lineshape and spin susceptibilities.     

Muon spin relaxation in different samples of DyAl2

Two samples of DyAl₂ were studied by longitudial μSR in the paramagnetic and ferromagnetic regime. In a region T_c±40 K the samples give different signals although X-ray analysis can not detect any impurity phase in either of them.