钙钛矿型锰氧化物(La$lt;sub$gt;0.8$lt;/sub$gt;Eu$lt;sub$gt;0.2$lt;/sub$gt;)$lt;sub$gt;4/3$lt;/sub$gt;Sr$lt;sub$gt;5/3$lt;/sub$gt;Mn$lt;sub$gt;2$lt;/sub$gt;O$lt;sub$gt;7$lt;/sub$gt;的磁性和电性研究

采用传统固相反应法制备钙钛矿型锰氧化物 (La_0.8Eu_0.2)_4/3Sr_5/3Mn₂O₇多晶样品, X-射线衍射分析表明, 样品(La_0.8Eu_0.2)_4/3Sr_5/3Mn₂O₇结构呈现良好的单相. 通过磁化强度随温度的变化曲线(M-T)、不同温度下磁化强度随磁场的变化曲线(M-H)和电子自旋共振谱发现: 在300 K以下, 随着温度的降低, 样品先后经历了二维短程铁磁有序转变 (T_C^2D ≈ 282 K)、三维长程铁磁有序转变(T_C^3D ≈ 259 K)、奈尔转变(T_N ≈ 208K)和电荷有序转变(T_CO ≈ 35 K); 样品 (La_0.8Eu_0.2)_4/3Sr_5/3Mn₂O₇在T_N以下, 主要处于反铁磁态; 在T_C^3D达到370 K时, 样品处于铁磁-顺磁共存态, 在370 K以上时样品进入顺磁态. 此外, 分析电阻率随温度的变化曲线(ρ-T)得到: 样品在金属-绝缘转变温度(T_P ≈ 80 K)附近出现最大磁电阻值, 其位置远离T_C^3D, 表现出非本征磁电阻现象, 其磁电阻值约为61%. 在T_CO以下, 电阻率出现明显增长, 这是由于温度下降使原本在高温部分巡游的e_g电子开始自发局域化增强所致. 通过对 (La_0.8Eu_0.2)_4/3Sr_5/3Mn₂O₇的ρ-T 曲线拟合, 发现样品在高温部分的导电方式基本遵循小极化子的导电方式. 关键词： 磁性 电性 金属-绝缘转变温度 电子自旋共振     

Specific heat and anisotropic superconducting and normal-state magnetization of HoNi2B2C

The magnetization of single-crystal HoNi₂B₂C has been measured as a function of applied field (H) and temperature in order to probe the interplay between superconductivity and magnetism in this complex layered system. The normal-state magnetic susceptibility of HoNi₂B₂C is highly anisotropic with a Curie-Weiss-like temperature dependence for H applied perpendicular to the c-axis and with a much weaker temperature dependence for H applied parallel to the c-axis, indicating that the Ho⁺³ magnetic moments lie predominately in the tetragonal a−b plane below 20 K. High-field magnetization (2000 Oe), low-field magnetization (20 Oe) and zero-field specific heat all give an antiferromagnetic ordering temperature of T_N=5.0 K. Remarkably, in 20 Oe applied field both superconductivity (T_c=8.0 K) and antiferromagnetism (T_N=5.0 K) clearly make themselves manifest in the magnetization data. From these magnetization data a phase diagram in the H−T plane was constructed for both directions of applied field. This phase diagram shows a non-monotonic temperature dependence of H_c2 with a deep minimum at T_N=5 K. The high-field magnetization data for H applied perpendicular to the c-axis also reveal a cascade of three phase transitions for T < 5 K and H < 15 000 Oe, contributing to the rich H versus T phase diagram for HoNi₂B₂C at low temperatures.     

Effect of pressure on the Néel temperature of the intermetallic compound YMn2

The effect of pressure on the Néel temperature T_N of the intermetallic compound YMn₂ has been studied up to 3.5 kbar by thermal expansion measurements. We have found that dT_N/dP is large and negative. T_N decreases nonlinearly with increasing pressure and becomes 0 at 3.7 kbar.     

Diamagnetic impurity effects on the Néel temperature in La2CuO4 and related materials

To investigate why the sensitivity of the Néel temperature T_N of the antiferromagnetic (AF) layered copper perovskites (typically La₂CuO₄) to diamagnetic impurities such as Zn is reportedly much larger than in the AF members of the K₂NiF₄ family, we first treat the effect of a concentration c of impurities on the uncorrelated electronic states in the coherent potential approximation (CPA). Then we consider the Heisenberg hamiltonian as the large correlation limit of the Hubbard hamiltonian for a single band of impurity-modified electronic states. The correlation effects are treated variationally. The model is solved explicity by using a rectangular density of states, and we obtain the c-dependent exchange J, staggered moment S_q, spin wave velocity and transverse susceptibility at zero temperature. We take into consideration several recently proposed formulae for T_N in the clean limit, and include the impurity effects by exploiting the results obtained, in order to test their predictions against the experimental T_N(c) data for La₂Cu_1−cZn_cO₄. Our results suggest that, to explain the difference between the K₂NiF₄ and the La₂ CuO₄ families, one should consider both the sign and the magnitude of the difference I≡ε^B−ε^A between impurity (B) and host (A) ionic potentials. The slowly decreasing trend of T_N(c) in the K₂NiF₄ family is reproduced if I is negative and sizeable, or positive but very small, while the quick decrease typical of the copper perovskites requires a positive and rather large I. For reasonable values of the interaction parameters, among the several models we compare, only the model of Chakravarty, Halperin and Nelson is able to semi-quantitatively reproduce the non-linear behaviour of T_N(c) reported for La₂Cu_1−cZn_cO₄, provided the spin stiffness is assumed to scale with c as appropriate to Fermi liquids.     

Coexistence of superconductivity and antiferromagentic order in Er2O2Bi with anti-ThCr2Si2 structure

We investigated the coexistence of superconductivity and antiferromagnetic order in the compound Er₂O₂Bi with anti-ThCr₂Si₂-type structure through resistivity, magnetization, specific heat measurements and first-principle calculations. The superconducting transition temperature T_c of 1.23 K and antiferromagnetic transition temperature TN of 3 K are observed in the sample with the best nominal composition. The superconducting upper critical field H_c2(0) and electron-phonon coupling constant λ_e−ph in Er₂O₂Bi are similar to those in the previously reported non-magnetic superconductor Y2O2Bi with the same structure, indicating that the superconductivity in Er₂O₂Bi may have the same origin as in Y₂O₂Bi. The first-principle calculations of Er₂O₂Bi show that the Fermi surface is mainly composed of the Bi 6p orbitals both in the paramagnetic and antiferromagnetic state, implying minor effect of the 4f electrons on the Fermi surface. Besides, upon increasing the oxygen incorporation in Er₂O_xBi, Tc increases from 1 to 1.23 K and T_N decreases slightly from 3 K to 2.96 K, revealing that superconductivity and antiferromagnetic order may compete with each other. The Hall effect measurements indicate that hole-type carrier density indeed increases with increasing oxygen content, which may account for the variations of T_c and T_N with different oxygen content.     

Structural changes in RNiO3 perovskites (R=rare earth) across the metal–insulator transition

Rare earth nickel oxide perovskites (RNiO₃, R=rare earth) have, except for LaNiO₃, a metal–insulator (MI) phase transition as temperature decreases. The transition temperature (T_MI) increases as the R-ion becomes smaller. They also present, at low temperatures, a complex antiferromagnetic order. For lighter R-ions (e.g. Pr and Nd), the antiferromagnetic transition temperature (T_N) is close to T_MI, while for heavier R-ions (e.g. Eu, Sm), T_MI and T_N are very far apart, suggesting that the magnetic and electronic behaviors are not directly coupled. Even though Ni³⁺ is a Jahn–Teller ion, no distortion in the NiO₆ octahedra was found for RNiO₃ perovskites with R=Pr, Nd, Sm and Eu. In this work we have measured EXAFS at Ni K edge for samples of PrNiO₃, NdNiO₃ and EuNiO₃. The Fourier transform spectra for the three samples show a clear splitting in the first peak at the insulating phase. This splitting corresponds to two or more different Ni–O distances. This indicates that there is either a distortion in the NiO₆ octahedra or there are two different Ni sites at the insulating phase.     

Magnetic and electronic phase transitions and magnetoresistance effect in the Pr0.5−xLaxSr0.5MnO3 (, 0.15) system

The electronic and magnetic phase transitions of Pr_0.5−xLa_xSr_0.5MnO₃ with x=0.10 and 0.15 were investigated. The M(T) and ρ(T) curves for these samples clearly show transitions from antiferromagnetic insulator to ferromagnetic semiconductor, ferromagnetic metal and finally to paramagnetic semiconductor as the temperature is increased from 5 to 300 K. Especially, two obvious protrudent peaks in the magnetoresistance curves MR(T) for these samples were clearly observed in the relative low magnetic field, 1 T. One peak appears at around the antiferromagnet-ferromagnet transition temperature T_N (150 K) with MR≈−23%, another occurs at around the ferromagnet-paramagnet transition temperature T_C(275 K ) with MR≈−8.2%. In addition, when the magnetic field was increased, the temperature corresponding to the MR peak at T_N shifts to lower temperature while the temperature corresponding to the MR peak at T_C is fixed.     

Luminescence spectrum from hexagonal YMnO3

Luminescence spectrum and its temperature dependence have been investigated for hexagonal YMnO₃ crystal which is ferroelectric below T_C=914 K and becomes simultaneously antiferromagnetic below T_N=74 K. The luminescence spectrum is as broad as two-magnon Raman scattering spectrum. The luminescence intensity is comparable to the latter at room temperature and it increases rapidly as the temperature decreases. These characteristics are discussed based upon other optical responses and theoretical results.     

Helimagnetism in the cubic Laves phase YMn2

Neutron diffraction experiments on YMn₂ using a wave length of λ_N = 2.483 Å show a splitting of the magnetic peaks. The magnetic structure is helimagnetic consistent with an angle modulation of the previously reported antiferromagnetic structure. The NMR spectrum can be explained as arising from a perturbation of the helix by the magnetocrystalline anisotropy. Below T_N the observed frustration of the negative Mn interactions is inherent from the topology of the crystallographic structure. Above T_N, it creates short range ordering whose thermal decrease may explain the increase in the paramagnetic neutron scattering as the temperature is increased.     

Spin ordering in the mixed-ligand antiferromagnet Mn(dca)2(pyrazine)

The flexibility offered by molecular-based systems allows us to introduce or replace specific ligands in a material with the aim of radically altering desired structural and magnetic properties. Specifically, Mn(dca)₂(pyz) {dca = dicyanamide, [N(CN)₂]⁻; PYZ = pyrazine} has a unique interpenetrating ReO₃-like lattice. The Mn²⁺ cations are high-spin ( ) and the material orders antiferromagnetically below T_N = 2.53(2) K. Using neutron powder diffraction we observed a collinear spin structure oriented along the short ac-diagonal of the monoclinic unit cell. Inelastic neutron scattering results show a magnetic excitation at 0.23 meV. The strong dispersion character of this excitation demonstrates that it is related to a low-energy spin wave. Upon warming, the magnon gradually softens and disappears at T_N, while critical scattering becomes evident by a broad quasielastic response above T_N. The energy of the magnon is consistent with the exchange parameter, J, derived from magnetic susceptibility measurements.     

Heat capacities of Laves phase compounds RMn2 (R = Y, Gd and Er)

Measurements of heat capacity indicate that the Mn moment in YMn₂ has an itinerant character and an additional C_M is observable even above T_N. In GdMn₂, the Gd moments are in disorder at T_N simultaneously with the Mn moments. The CEF contributions in ErMn₂ are observed and are calculated using a single-ion Hamiltonian.     

Re-entrant ferrimagnetism in TbMn6Ge6

The magnetic ordering of the hexagonal compound TbMn₆Ge₆ has been studied by neutron diffraction at various temperatures between 1.8 and 500 K. In almost the whole magnetically ordered regime the magnetic structures are incommensurate with the crystal lattice. The corresponding wave vector q₁ = (0,0,q_z) is strongly temperature dependent and decreases from q_z = 0.1307 r.l.u. at 1.8 K to q_z = 0.091 r.l.u. at 410 K. The low-temperature range (T < 85 K) is characterised by a triple ferrimagnetic spiral structure with net moment along the c-direction. At T_t = 85 K the net moment disappears and the magnetic ordering changes into a flat spiral structure that probably persists up to the magnetic ordering temperature, T_N = 450 K. Before reaching the magnetic ordering temperature, however, an additional ferrimagnetic component perpendicular to the c-direction develops, marking the onset of re-entrant ferrimagnetism. The resulting structure described by two propagation vectors corresponds to a distorted spiral. Various models are discussed. The observed re-entrant ferrimagnetism is in agreement with results of previously reported magnetic measurements.     

The nuclear contribution to the specific heat of single crystals of YBa2Cu3O7 and Bi2Sr2CaCu2O8

Specific heat data below 1 K of Bi₂Sr₂CaCu₂O₈ and YBa₂Cu₃O₇ are analyzed. For YBa₂Cu₃O₇ the nuclear specific heat, C_N, amounts to 38T⁻² μJ/mol K. C_N for Bi₂Sr₂CaCu₂O₈ exceeds that of YBa₂Cu₃O₇ by a factor of 15. The nuclear quadrupolar specific heat contribution alone is insufficient to explain the data for YBa₂Cu₃O₇, while lack of NQR data does not allow such a comparison in Bi₂Sr₂CaCu₂O₈ to be made. The contribution to C_N from nuclear spins coupled via the contact hyperfine interaction with correlated magnetic spins (in the CuO₂ plane) is derived as a function of the correlation length. This contribution can be treated independently from the quadrupolar term. We show that the excess specific heat in YBa₂Cu₃O₇ likely originates in a few percentage of an impurity (oxygen deficient) phase with a strong hyperfine field on the Cu nuclei.     

Disruption of antiferromagnetic order in Zn-doped La2CuO4

The magnetic phase diagram of La₂(Cu_1−xZn_x)O₄ has been determined from zero-field muon-spin-rotation (ZF-μSR) data taken at LAMPF for 0 ≤ x ≤ 0.10. Antiferromagnetic onset temperatures follow T_N(x) from susceptibility measurements on the same samples. However, the order becomes long range, as evidenced by a well-defined internal magnetic field, only at temperatures well below T_N. Extrapolation of our results yields T_N → 0 K at x = 0.11 for a single (Cu_1−xZn_x)O₂ plane, and comparison with YBa₂(Cu_1−xZn_x)₃O₆ implies identical disruption of magnetism by Zn doping in the single- and double-plane systems.     

Magnetic Raman optical activity in FeF2

Raman optical activity (ROA) of magnons and phonons in antiferromagnetic FeF₂ (T_N=78 K) has been studied as a function of temperature and in applied magnetic field. For exciting light incident along the rutile-structure c-axis, ROA is observed for magnons but not phonons. In zero field, the small anisotropy-induced splitting (0.09 cm⁻¹) of the two acoustic-magnon branches is observed by light scattering for the first time. The splitting in applied magnetic field is found to reduce with increasing temperature in accordance with theory. No ROA was detected for two-magnon excitations.     

K2NiF4型Sr2CrO4的磁电性质研究

以SrO和CrO₂为原料, 在高温高压的条件下直接反应生成纯相的K₂NiF₄结构的Sr₂CrO₄多晶样品. 结构用粉末X射线衍射及GSAS精修表征. 磁化率测试显示样品存在一个弱的反铁磁相变, 奈尔温度为T_N=95 K. 在奈尔温度以上, 磁化率随温度的变化遵循居里-外斯定律. 对样品进行了电阻测试, 结果显示了样品的绝缘特性.     

Spin fluctuations in the paramegnetic state of YMn2

Polarisation neutron diffusion and polarisation analysis has been performed on YMn₂ in the paramagnetic state up to 3T_N. Results revealed an important scattering at all temperatures, it remains strongly enhanced about the staggered antiferromagnetic wave vectors. Furthermore, the amplitude of the diffusion increases with temperature.     

Antiferromagnetism of the hexagonal Laves phase ThMn2

Magnetization, thermal expansions and neutron diffraction measurements have been performed on ThMn₂. Below T_N, one Mn atom (2a) in four remains nonmagnetic whilst the others order in a triangular configuration. The large anistropic thermal expansions effects minimize the frustration of the Mn-Mn interactions.     

Low-temperature phase and magnetic interactions in FCC Fe-Cr-Ni alloys

The low-temperature (5 K < T < 300 K) magnetic properties of a set of nine isostructural fcc Fe-Cr-Ni (Fe ≈ 68 at %, Cr ≈ 20 at%, Ni ≈ 9 at%) alloys were studied by SQUID magnetometry, neutron diffraction and ultrasonic techniques. Type-1 antiferromagnetic (AF) ordering was observed below the Néel temperature, T_N. The dc susceptibility, χ(T), did not exhibit a simple Curie-Weiss dependence. Above T_N, atemperature independent component χ₀ was observed, i.e., χ(T) = χ₀ + C / (itT + θ. T_N was systematically influenced by the lattice parameter, a, decreasing from (47.9 ± 0.5) K to (35.0 ± 0.5) K as a increased by only 0.25%. The average magnetic moment of ≈ 0.6μ_B obtained from neutron scattering was lower than the ≈ 1 μ_B obtained from the SQUID data. Mean field estimates of antiferromagnetic nearest-neighbors exchange interaction (J₁) and ferromagnetic second-nearest-neighbors interaction (J₂) indicate that |J₂/J₁|≈ 1.5. We believe that this is evidence of the RKKY interaction, and self-consistently argue that only the external d electrons are responsible for the localized average moment. This may mean that s-d hybridization of the external electrons is weak in these alloys.     

Incommensurate antiferromagnetic structures in NdIn3

Among the AuCu₃-type RIn₃ series where R is a rare earth, the NdIn₃ compound presents a complex magnetic phase diagram. In this compound, which orders antiferromagnetically at T_N = 5.9 K, three magnetic phases are separated by two sharp first-order transitions. The phase diagrams, determined for the main crystallographic directions, by magnetization measurements in fields up to 7 T show a strong dependence of the transition temperatures. In order to determine the actual magnetic structures in NdIn₃, a neutron diffraction experiment has been performed on a single crystal under magnetic field. It shows that the magnetic structures are collinear (single q) with the magnetic moments aligned along the fourfold axis. They clearly evidence the existence of two incommensurate phases with q = (1/2, 1/2, τ): for T_N T 5.5 K, τ₁ ≈ 0.037 2π/a and the structure is sine-wave modulated, for 5.5 K > T > 4.7 K, τ₂ = 0.017 2π/a and the structure squares up. Below 4.7 K the q = (1/2, 1/2, 0) commensurate structure is stabilized.