Exchange bias effect in multiferroic Eu0.75Y0.25MnO3

The exchange bias phenomenon has been investigated in multiferroic Eu_0.75Y_0.25MnO₃. The material shows a weak ferromagnetism with cone spin configuration induced by external magnetic field below 30 K. Consequently, the electric polarization coming from the cycloid spin order below 30 K can be suppressed by external magnetic fields. The magnetic hysteresis loops after cooling in a magnetic field exhibit characteristics of exchange bias below the spin glassy freezing temperature (T_g)∼16 K. The exchange bias field, coercivity field, and remanent magnetization increase with increasing cooling magnetic field. The exchange bias effect is ascribed to the frozen uncompensated spins at the antiferromagnetism/weak ferromagnetism interfaces in the spin-glass like phase.     

Energy levels and crystal-field analysis of Tm in YAl3(BO3)4 crystals

The electronic structure of the Tm³⁺ in YAl₃(BO₃)₄ crystals has been investigated by means of low temperature absorption and emission spectroscopy in the 5000-30,000 cm⁻¹ range. The assignment of the lines composing the observed manifolds to transitions between the Stark levels of Tm³⁺ is complicated by the presence of extra features having different origins. The energy levels scheme of the doping ion has been compiled after a careful analysis of the spectra by reproducing the observed transitions by means of theoretical calculations based on a Hamiltonian, including the free ion and the crystal field (CF) terms. The agreement between experimental and calculated energy values was reasonably good, the overall r.m.s. deviation being 16 cm⁻¹. The resulting CF parameters have been tabulated and compared with those reported in literature for other rare earth ions doped in YAB. The analysis of trends observed along the lanthanide series evidences some inconsistencies and the necessity of a systematic investigation of these systems.     

Electrical behavior of nano-polycrystalline (La1−yKy)0.7Ba0.3MnO3 manganites

We present a study of the structural and electrical behavior of nano-polycrystalline mixed barium and alkali substituted lanthanum-based manganite, (La_1−yK_y)_0.7Ba_0.3MnO₃ with y=0.0-0.3. The samples were synthesized by the polymerization complex sol-gel method. The powder X-ray diffraction (XRD) data of the samples show a single-phase character with space group. The magnetic and electrical transport properties of the nano-polycrystalline samples have been investigated in the temperature range 50-300 K and a magnetic field up to 10 kOe. The metal-insulator transition temperature T_p of all the samples decreased with potassium doping, and also, it increased slightly with the application of magnetic field. The low field magnetoresistance, which is absent in the single-crystalline perovskite, was observed and increased with decreasing temperature. Comparing the experimental resistivity data with the theoretical models shows that the high temperature electrical behavior of these samples is in accordance with the adiabatic small polaron-hopping model. In the metal-ferromagnetic region the resistivity is found to be quite well described by ρ=ρ₀+ρ₂T²+ρ_4.5T^4.5.     

Study of molybdenum coordination state and crystallization behavior in MoO3-La2O3-B2O3 glasses by Raman spectroscopy

The ternary MoO₃-La₂O₃-B₂O₃ glasses containing a large amount of MoO₃ (10-50 mol%) are prepared, and their structure and crystallization behavior are examined from the Raman scattering spectrum measurements and X-ray diffraction analyses. It is found that the glass transition and crystallization temperatures and the thermal stability against crystallization decrease with increasing MoO₃ content. It is suggested that the main coordination state of Mo⁶⁺ ions in the glasses is isolated (MoO₄)²⁻ tetrahedral units giving strong Raman bands at 830-860 and 930 cm⁻¹. It is found that the crystalline phases in the crystallized glasses are mainly LaMoBO₆ and LaB₃O₆, and the main crystallization mechanism in MoO₃-La₂O₃-B₂O₃ glasses is surface crystallization. LaMoBO₆ crystals are found to give strong Raman bands at 810-830 and ∼910 cm⁻¹.     

正铁氧体SmFeO_3高压拉曼研究(英文)

本文主要通过高压拉曼光谱研究了正铁氧体SmFeO3的晶格振动模式在外加压力作用下的行为规律,高压实验中压力最高为29.7GPa。本文采用溶胶凝胶法,制备出具有正交结构,其空间群为Pnma的SmFeO3。在外加压力作用下,所有观察到的拉曼振动模式都呈现出宽化趋势。特别是位于621.1cm-1的FeO6八面体的反弹性振动模式Ag(1)与位于452.7cm-1的FeO6八面体的弯曲振动模式B3g(3),其压力系数出现最大值。与此相反,Sm-O振动模式Ag(7)的压力系数却非常小。这说明外加压力更容易影响到FeO6八面体的晶格变化,而不是SmO12十七面体的改变。SmFeO3的这种高压下晶格振动模式变化行为类似于G型结构的CaSnO3。同时,文中还给出了所有声子零压模式下的格林爱森参数与体弹模量的比值。这些参数可用于进一步测量单轴或者双轴的应变力,可深入理解声子频率在张力作用下移动的表现行为。     

Na2CO3的高压拉曼光谱研究

碳酸盐是碳在地球内部的重要载体之一,其在地幔高温高压条件下的晶体化学是理解地球深部碳的赋存状态和循环过程的关键,而结构稳定性和相变是晶体化学最基本的研究内容。碳酸钠（Na₂CO₃）是一种常见的碱性碳酸盐矿物,在产自地幔过渡带-下地幔的金刚石中已发现含钠的碳酸盐矿物包裹体,这成为碳酸钠能够俯冲进入地幔深部的直接矿物学证据。前人利用拉曼光谱技术研究了Na₂CO₃在常温常压下的晶格振动模式,但其在高压下的稳定性和结构变化却鲜有报道。利用金刚石压腔装置结合先进的共聚焦拉曼光谱技术,以硅油作为传压介质,在准静水压力条件下,在0.001～27.53 GPa压力区间对Na₂CO₃粉末在600~1 200 cm-1波段的振动特征进行了细致地分析。本次实验重点分析了[CO₃]2-基团振动模式在升压和卸压过程中的行为。结果表明,在0.001～11.88 GPa压力范围内,[CO₃]2-基团对称伸缩振动γ₁（1 088.06和1 070.76 cm-1）、反对称伸缩振动γ₃（865.10和797.50 cm-1）和面内弯曲振动γ₄（720.10和696.71 cm-1）都出现了振动峰的分裂。随着压力增加,所有振动峰都向高频率漂移,半高宽也逐渐增加。在13.40 GPa时,Na₂CO₃发生结构相变,具体表现为690.08 cm-1处出现1条新的拉曼峰,并且随着压力升高该峰的强度逐渐增大。同时反对称伸缩振动峰γ₃以及面内弯曲振动峰γ₄的强度持续减弱,半高宽也继续变大。这些现象表明Na₂CO₃结构相变源于[CO₃]2-内部晶格变化。当压力卸载到4.18 GPa时,[CO₃]2-的振动模式与常温常压下的完全吻合,相变出现的新峰也已经消失,表明该相变是由[CO₃]2-基团畸变引起的并且具有可逆性。继续升压至27.53 GPa,拉曼光谱继续蓝移,Na₂CO₃的拉曼谱线再没有变化,说明高压相在这一压强范围内保持稳定。在整个加压过程中,反对称伸缩振动γ₃和面内弯曲振动γ₄处的拉曼峰出现强度减弱现象。同时也计算了各个峰频率对压力的依赖系数dγ/dP,结果显示[CO₃]2-基团内各个振动模式对压力的响应是不同的,这很可能与Ｃ-Ｏ键的键长有关。最后,对比发现,对称伸缩振动γ₁峰的强度比反对称伸缩振动γ₃和面内弯曲振动γ₄峰的强度大,并且[CO₃]2-基团对称伸缩振动γ₁受压力影响相对较小,可以用来区别不同种类的碳酸盐矿物。     

Study of magnetic properties of La2/3Sr1/3MnO3 nanotubes by Monte Carlo simulation

Magnetic properties of a single nanotube whose walls are constituted by nanograins of La_2/3Sr_1/3MnO₃ are studied by means of Monte Carlo (MC) simulation. The system is considered as composed by ferromagnetic grains which couple via dipolar interaction. The grain size distribution is obtained from experimental measurements and the inter-grain distance distribution is obtained from a study of distance distribution among magnetic particles distributed in the tube walls. We show the magnetization behavior for a tube of 700 nm of diameter and 3.5 μm length. We discuss the simulation for different temperatures and external fields. As a main result, we show that the distribution of inter-granular distances has a unique behavior for tubular structures of similar diameter/length aspect ratio, independent of their sizes. This scaling relation allows us to perform the simulations using a tube of smaller dimensions. We succeed in explaining the magnetization curves, finding that dipolar interaction is necessary to explain the experimental behavior and that the grains behave as having magnetic dead layers.     

Phase transition in multiferroic YMnO3 and its solid solution YMn(0.93)Fe(0.07)O3

Ceramics of YMnO₃ and its Fe substituted YMn_(0.93)Fe_(0.07)O₃ solid solution were synthesized by solid state reaction of the oxides at 1200 °C. Hexagonal phase was identified in both cases by X-ray powder diffraction. Rietveld refinement of cell parameters showed an increase of the parameter values for the solid solution. Dielectric permittivity measurements versus temperature showed a phase transition at 655 °C for yttrium manganite, however, for the solid solution no phase transition was detected on heating up to 700 °C. Dielectric loss measurements showed higher slope changes and better defined local maxima for the solid solution than for the pure phase.     

Ferroelectric,magnetoelectric and photoelectric properties of BiFeO3 /LaNiO3 heterostructure

BiFeO₃/LaNiO₃ (BFO/LNO) heterostructure was fabricated on quartz substrate via RF sputtering method. The microstructure and surface morphology of the BFO/LNO heterostructure was demonstrated. BFO layer shows good ferroelectric and weak ferromagnetic characters at room temperature. The dielectric constants of the heterostructure under an applied magnetic field 1.2T and zero field are both decreased with increasing frequency at room temperature and the dielectric constant under the applied magnetic field is larger, which is attributed to the coupling between the electric and magnetic dipoles, and further demonstrated in the framework of the Ginzburg-Landau theory for second phase transition. Additionally, the photoconductivity of the heterostructure under blue-laser illumination was observed, and the photoconductivity increase with the enhanced power of the blue-laser.     

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.     

Dielectric properties of BaTiO3-CoFe2O4 nanocomposite thin films

We report on the dielectric characterization of CoFe₂O₄-BaTiO₃ nanocomposites grown by rf sputtering. Dielectric properties have been analyzed for samples grown at different deposition temperatures and with different thicknesses. Impedance spectroscopy data has been analyzed by fitting to an equivalent circuit and different contributions have been identified. Correlations between dielectric properties and deposition temperature and thickness have been established.     

Spin polarized La0.7Sr0.3MnO3 thin films on silicon

La_0.7Sr_0.3MnO₃ polycrystalline manganite thin films were grown on silicon (Si) substrates covered by SiO_x amorphous native oxide. Curie temperatures of about 325 K were achieved for 70-nm-thick films. Strong room temperature XMCD signal was detected indicating high spin polarization at the surface. Cross-sectional TEM images show sharp interface between SiO_x and manganite without signature of chemical reaction at the interface. Unusual sharp splitting of the manganite film was observed: on the top of a transition layer characterized by low crystalline order, a magnetically robust layer is formed.     

EPR evidence of local lattice mode in K3H(SO4)2 and Rb3H(SO4)2 fast-proton conductors

The observation of an anomalous temperature dependence of Mn²⁺ EPR spectra linewidth and nonaxial crystal-field parameter in K₃H(SO₄)₂ and Rb₃H(SO₄)₂ allows one to suggest the presence of “local mode” predicted by Yamada (Ferroelectrics 170 (1995) 23). The activation energy for this kind of excitation was found and equals 11.3 (0.5) and 7.4 (0.3) meV for Mn²⁺ doped K₃H(SO₄)₂ and Rb₃H(SO₄)₂, respectively.     

Ge_x Si_(1-x)/Si超晶格中纵声学声子的喇曼散射强度研究

本文用光弹理论,在全面考虑了超晶格中两种材料的声速,质量密度和光弹常数存在差别的基础上,计算了Ge_xSi_(1-x)/Si超晶格中折迭纵声学声子的喇曼散射强度,在高达50cm~(-1)的频率范围内,理论值和实验符合得很好。     

The relation between magnetoresistance and magnetocaloric effect in La0.85Ag0.15MnO3 manganite

We present the temperature dependence of La_0.85Ag_0.15MnO₃ resistivity in the temperature interval between 77 and 340 K and magnetic fields up to 26 kOe. We offer a method of separating tunnel magnetoresistance from total magnetoresistance. A change in both the magnetic entropy, which is caused by the magnetocaloric effect (MCE), and the magnetoresistance are shown to be connected through a simple relationship to La_0.85Ag_0.15MnO₃.     

Multiferroic behaviors of Co-doped Bi4NdTi3FeO15 ceramics

By using a multicalcination procedure, Co-doped Bi₄NdTi₃Fe${}_{1?x}$Co_xO₁₅ ($x=0.1,0.3,0.5\text{ and }0.7$) (Co_x) ceramics were synthesized. The samples showed a single-phase (SP) Aurivillius structure containing four perovskite layers. Plate-like morphology of the grains which is related to the layered perovskite structure of the samples was clearly observed by SEM. The multiferroic properties of the samples at room temperature (RT) were demonstrated by dielectric, ferroelectric and magnetic measurements. With x ranging from 0.1 to 0.7, all the samples show RT multiferroic properties although there is no obvious regularity between the Co content and the multiferroic property. Very interestingly, Co_0.3 sample exhibits the optimum RT magnetic property, which can be attributed to the inclination of occupying the inner octahedra center for doped Co ions and the nearly 1:1 ratio of Fe and Co ions in the inner octahedra. The present work offers new insight into the compositional design of promising lead-free RT multiferroic materials.     

A high-pressure Raman and X-ray diffraction study of the perovskite SrCeO3

A high-pressure structural study of SrCeO₃ has been performed at room temperature by Raman spectroscopy and X-ray diffraction up to 32 and 45 GPa, respectively. A first-order reversible phase transition is observed at about 12 GPa in both techniques. A second weak structural change, taking place between 18 and 25 GPa, can be suspected from Raman data. The increase in the number of Raman bands and diffraction lines is an indication that the symmetry is lowered and the compound does not evolve towards the ideal cubic perovskite structure. A Rietveld analysis of X-ray data was performed for the low-pressure phase and the atomic positions and the cell lattice parameters variations are reported in this paper. The volume compressibility derived from Raman modes (5.6×10⁻¹² Pa⁻¹), involving mainly bond-stretching for each type of polyhedron, is found to be close to the one obtained from volume cell variations measured by X-ray diffraction (7.9×10⁻¹² Pa⁻¹).     

Giant magnetoimpedance and permeability change in La2/3Sr1/3MnO3 manganite under low fields

We demonstrated that La_2/3Sr_1/3MnO₃ sintered manganite could exhibit a magnetoreactance ΔX/X₀ of −25.5% at 100 kHz, a giant magnetoimpedance ΔZ/Z₀ of −20% at 1-2 MHz and a giant AC magnetoresistance ΔR/R₀ of −39.3% at 5 MHz under a very low field of 300 Oe at room temperature, whereas the DC magnetoresistance Δρ/ρ₀ was −3.95% under H=10 kOe and only about −0.18% under H=300 Oe. Large field-induced change of real and imaginary circular permeabilities (Δμ′_?/μ′_?(0) and Δμ″_?/μ″_?(0)) were obtained for La_2/3Sr_1/3MnO₃ sintered manganite. The giant magnetoreactance (giant magneto-inductive effect) at very low frequencies originates from the field induced change of transverse permeability. At 100 kHz under H=300 Oe, La_2/3Sr_1/3MnO₃ sintered manganite has Δμ′_?/μ′_?(0)=−25.8% and Δμ″_?/μ″_?(0)=−10.9%. The values of ΔR/R₀ and ΔZ/Z₀ are very small under 300 Oe at 100 kHz. The giant magnetoimpedance at high frequencies mainly originates from the large transverse permeability change induced by DC magnetic fields, via the penetration depth. Under H=300 Oe, La_2/3Sr_1/3MnO₃ sintered manganite presents values of Δμ′_?/μ′_?(0)=−24.9%, Δμ″_?/μ″_?(0)=−49.8% at 1 MHz, and Δμ′_?/μ′_?(0)=−21.2%, Δμ″_?/μ″_?(0)=−58.2% at 5 MHz.