Current induced deformation of charge density waves in orthorhombic TaS3

The low electric field ohmic resistance R of orthorhombic TaS₃ measured at 90 and 120 K well below the Peierls transition temperature depends on the product of a temperature difference ΔT applied along the sample and the sign of a previously applied current pulse if this pulse is larger than threshold for non-ohmic conductivity. This resistance change is about ΔR/RΔT ∽ 1×10^-3 K^-1 for a pure sample and ΔR/RΔT ∽ 6×10^-3 K^-1 for a slightly electron irradiated one at 90 K. The relative resistance change is insensitive to the sample length. We deduce that the CDW current changes inhomogeneously the Peierls gap E_g. ΔE_g < O at the contact where the CDW current enters and ΔE_g > O at the exit. The effect is attributed to a CDW current induced inhomogeneous deformation of the CDW itself.     

Coupling of the CDW and the water mode in K2Pt(CN)4Br0.3⋯3.2H2O

In previous work we have observed the amplitude mode of the charge density wave (CDW) in K₂Pt(CN)₄Br_0.3?3.2H₂O (KCP) by means of Raman scattering. New measurements made on deuterated material, K₂Pt(CN)₄Br_0.3?3.2D₂O (KCP1), show the same mode but shifted from 44 to 38 cm_?1, maintaining the symmetry properties and temperature dependence of frequency and linewidth. This considerable isotope effect is interpreted in terms of a coupling of the CDW with the water stretching mode, which by the deuteration is shifted from 3494 cm^?1 in KCP to 2560 cm^?1 in KCP1 according to the change in atomic mass. Both of these modes exhibit A₁(z) symmetry. At 5 K the resulting decoupled frequency of the CDW amplitude mode is 57 cm^?1, and the coupling energy about 140 cm^?1. A discussion of the temperature dependence of various important quantities is given. The present results show that the water molecules, which are located in between the Pt chains are strongly involved in the eigenvector of the CDW amplitude mode.     

X-ray evidence for a deformation of CDW during the sliding motion in K0.30MoO3

The wave vector and the correlation length of the CDW ordering in K_0.30MoO₃ are studied by x-ray diffraction as functions of electric fields applied along the one-dimensional axis. Several samples change their CDW-ordering above a threshold field. The change of the wave vector occurs mainly in the (2a¹-c¹) - direction, which is perpendicular to the one-dimensional b¹ - axis. It depends also on the field direction and magnitude. Time resolved x-ray experiments show that characteristic time of this change is of the order of 1 ms. The correlation length becomes longer along the (2a¹-c¹)-direction in the transient period.     

Raman study of charge-density-wave phase transition in quasi-one-dimensional conductor (TaSe4)2I

Polarized Raman spectra were obtained in the quasi-one-dimensional conductor (TaSe₄)₂I above and below the charge-density-wave (CDW) transition temperature (T_c=263 K). The Raman intensities of many peaks become intenser and two of the phonon peaks shift to higher frequency with decreasing temperature. Moreover a new broad peak at about 90 cm^?1 and a new peak around 166 cm^?1 appear in the low-temperature phase. The polarization characteristic shows that the former is assigned to totally symmetric mode. The damping constant of the phonon at 90 cm^?1 increases markedly with increasing temperature. The frequency shifts to higher frequency as the temperature increases and the coupling coefficient is approximately proportional to (T_c?T)^{$\text{1}\text{2}$}. This peak becomes Raman active owing to the CDW phase transition. The temperature dependence of the damping constant and the frequency shift may have a relation to the dynamical properties of the CDW phase transition.     

Far infrared optical properties of NbSe3

We have measured the far infrared reflectance of NbSe₃ and used models of the frequency dependent conductivity to fit the data. General arguments show that at 2 K a charge density wave (CDW) energy gap exists between 120 and 190 cm^?1, the relaxation time(s) of the free carriers and CDW pinned mode is >30×10^?12 s, and the ratio of the free carrier concentration to band mass is <2×10²⁰ cm^?3/m₀.     

Charge density wave depinning and switching in NbSe3

We have investigated the relation between charge density wave (CDW) depinning and switching in NbSe₃. In the lower CDW state we observe that the critical electric field at which switching occurs is independent of temperature. We also observe that the differential resistance of the sample is independent of applied dc bias beyond the switching threshold, and corresponds to the high-field limit of the pure resistance. We interpret our results in terms of a temperature dependent CDW domain structure in the crystal.     

Size effects on the charge-density-wave pinning in the quasi-one-dimensional conductor K0.30MoO3

We report size effects on the charge-density-wave pinning in the quasi-one-dimensional conductor K_0.30MoO₃ in the temperature range 77 K-160 K. The threshold field is approximately one order of magnitude larger in needle-like samples than in bulk crystals, temperature independent and strongly dependent on the width of the sample. In addition, the nonlinear conductivity shows a maximum near 130 K. The results are discussed in relation with various pinning models and CDW dislocations.     

On the nonlinear field-effect of orthorhombic TaS3

The true d.c. measurement of electrical field effect on the resistivity of orthorhombic TaS₃ in the CDW state was performed for the first time with extremely short distances between the contacting leads. Very weak nonlinear effect was observed up to 1300 V cm^?1. A distinct resistivity — increasing effect was found, which cannot be understood within the framework of any currently available theories. We propose a transverse tunneling model to account for this anomaly.     

Spin- and charge-density-wave orders in La1.87Sr0.13Cu0.99Fe0.01O4

We have performed elastic neutron-scattering measurements on La_1.87Sr_0.13Cu_0.99Fe_0.01O₄ to study the magnetic impurity effects on the stripe correlations in high-T_c cuprates. Both charge-density-wave (CDW) and spin-density-wave (SDW) orders are observed in the low-temperature-orthorhombic (LTO) phase for the first time. With decreasing the temperature, CDW order first appears at followed by the SDW order at lower temperature of . The incommensurability for the CDW order (ε) was found to be 0.224±0.002 r.l.u., which is approximately twice of that for SDW order (δ) of 0.115±0.003 r.l.u. Both ordering sequence and relation of ε≈2δ are the same for SDW and CDW orders observed in the low-temperature-tetragonal (LTT) phase of La_1.60-xNd_0.4Sr_xCuO₄ (LNSCO), suggesting that the similar stripe correlations exist in the cuprate oxides, irrespective of crystal structure.     

Non-linear conductivity of monoclinic TaS3

Strongly non-ohmic conduction is observed in the semiconducting charge-density-wave (CDW) state of monoclinic TaS₃ above a very sharp threshold field. These features could be interpreted in terms of depinning or tunneling of pinned CDW under applied electric field. We also found that large noise appears with the onset of the non-linear conductivity and fades away as the current through the samples is increased, which behaves as the decreasing function of frequency.     

Thermal expansion measurements of the quasi-one-dimensional conductor K0.30MoO3

The charge density wave (CDW) dynamics of the quasi-one-dimensional conductor K_0.30MoO₃ shows two different regimes depending on the temperature: a strongly damped CDW motion above ∼50 K and CDW motion with almost no damping below ∼50 K. In a search for a characterization of this CDW behaviour, we performed thermal expansion measurements on K_0.30MoO₃ single crystals in the temperature range 4-250 K. In addition to the anomaly observed at the Peierls transition at 180 K along the [102] direction, an anomaly is observed at ∼50 K along the [−201] and [102] directions. The results are discussed in relation with the change in the CDW rigidity at ∼50 K.     

横向交、直流电流对蓝青铜K0.3MoO3的I-V特性的调制效应

通过I-V特性测量，研究了横向交、直流电流对蓝青铜K_0.3MoO₃中电荷密度波(CDW)动力学行为的影响.实验结果表明，无论是直流还是交流，随着横向调制电流的增大，CDW滑移的阈值电场均会相应地减小；但横向交流电流的调制效应较小，可能更接近本征的效应.考察了横向交流电流的调制效应与其频率的依赖关系. 关键词： 0.3MoO₃单晶')" href="#">K_0.3MoO₃单晶 电荷密度波 横向电流调制效应     

Quasiperiodic noise voltage and metastability in the charge density wave conductivity of K0.30MoO3

Slow relaxation phenomena as well as quasiperiodic noise have been studied in the non linear regime of conductivity which takes place above a well defined threshold electric field in the semiconducting incommensurate phase of the quasi one-dimensional blue bronze K_0.30MoO₃. The noise frequencies are found to be proportional to the excess current attributed to the charge density wave (CDW). In some temperature range, the CDW current is found to decrease logarithmically vs time. These results indicate the presence of metastable states related to domains and domain walls.     

CDW evidence in one-dimensional K0.3MoO3 by means of Raman scattering

Raman scattering measurements on the one-dimensional (1-D) blue bronze K_0.3MoO₃ are reported as function of temperature. At about 50 cm^-1 a Raman line of A_g(A) symmetry was found with an anomalous temperature dependence. The line symmetry, the softening of the eigenfrequency and the apparent disappearing of the coupling constant at the critical temperature, allow us to assign this line to the amplitude mode of the CDW, predicted by the theory of the Peierls transition. A Peierls precursor at room temperature was also observed and is discussed.     

Hydrothermal synthesis and Magnetocaloric effect of La0.5Ca0.3Sr0.2MnO3

The hydrothermal synthesis and magnetic entropy change for the perovskite manganite La_0.5Ca_0.3Sr_0.2MnO₃ have been studied. The La_0.5Ca_0.3Sr_0.2MnO₃ can be produced as phase-pure, crystalline powders in one step from solutions of metal salts in aqueous potassium hydroxide solution at a temperature of 513 K in 72 h. Scanning electron microscopy shows that the materials are made up of cuboid-shaped particles in typical dimension of 4.0×2.5×1.6 μm. Heat treatment can improve the magnetocaloric effect for the hydrothermal sample. The maximum magnetic entropy change ΔS_M for the as-prepared sample is 0.88 J kg⁻¹ K⁻¹ at 315 K for a magnetic field change of 2.0 T. It increases to 1.52 J kg⁻¹ K⁻¹, near its Curie temperature (317 K) by annealing the sample at 1473 K for 6 h. The hydrothermal synthesis method is a feasible route to prepare high-quality perovskite material for magnetic refrigeration application.     

Effect of surface-topology on magnetic properties in (La0.6Eu0.4)0.67Ca0.33MnO3 of anisotropic shape of nanoplates

(La_0.6Eu_0.4)_0.67Ca_0.33MnO₃ has been prepared in the shape of nanoplates of single crystallites (an orthorhombic structure) through polymer templates. HRTEM images reveal 18, 25, and 30 nm thicknesses of plates after heating a precursor powder at 873, 1073, and 1273 K in air for 2 h. These values present average crystallite size determined from broadening of the X-ray diffraction peaks. A spin-glass-like surface (GS) overlayer (3-5 nm thickness) in such plates facilitates a ferromagnetic→ferrimagnetic reordering with markedly suppressed Curie point T_C, i.e., as small as 90 K in a 873 K heated sample, from the parent value 268 K. The T_C point increases to 103 K (or 120 K) when heating at higher temperature 1073 (or 1273 K), during which the core grows at the expense of the overlayer. The GS tailors as high coercivity H_c as 617 Oe in the zero field cooled (ZFC) sample that is decreased to 500 Oe in the field cooled (FC) sample in the surface spin-freezing along the field direction. The H_c-value (ZFC) that steps down successively to 252 Oe on the overlayer is thinned down by heating at 1273 K. Samples heated at 873, 1073, or 1273 K have regularly increased saturation magnetization 35.3, 63.9, or 69.6 emu/g in ZFC, while 43.7, 70.2, or 75.5 emu/g in FC measured at 10 K. The ferrimagnetic reordering are described based on the scenario of an antiferromagnetic exchange coupling between the Eu³⁺ and Mn³⁺ (or Mn⁴⁺) sublattices.     

Valence states of iron ions in nanostructured yttrium iron garnet Y3Fe5O12 studied by means of soft X-ray absorption spectroscopy

Nanostructured samples of yttrium iron garnet Y₃Fe₅O₁₂ obtained by plastic deformation method (high-pressure torsion) were studied with help of soft X-ray absorption spectroscopy using Fe 2p and O 1s spectra. Experimental spectra were compared with crystal field multiplet calculations for Fe ions. Some amount of Fe²⁺ ions in nanostructured Y₃Fe₅O₁₂ was found. The concentration of Fe²⁺ ions was found to be increased with the increase of the degree of plastic deformation.     

H2O2氧化法制备Fe3O4纳米颗粒及与共沉淀法制备该样品的比较

在近中性条件下，利用H₂Ｏ₂氧化Fe(OH)2胶体成功制备了Fe₃ Ｏ₄纳米颗粒.分别利用透射电镜(TEM)，x射线衍射仪(XRD)，振动样品磁强计(VSM)和超导量子干涉仪（SQUI D）对样品的形貌，结构，宏观磁性进行了表征和测量.TEM图像表明样品为球形颗粒，直径 大小约18nm，且分布较均匀.XRD结果表明样品为立方尖晶石结构.穆斯堡尔谱测量表明样品 室温下对应两套六线谱，样品的晶体结构存在缺陷，内磁场略小于块体Fe₃Ｏ4的值. 宏观磁测量表明样品的饱和磁化强度可达67×10^-3A·m²/g，在20 K出现了Verw ey转变.选择该法制备的Fe₃Ｏ₄纳米颗粒与共沉淀法得到的样品作 了磁性比较.宏观磁 测量表明共沉淀法制备的样品在外磁场为1T时仍未饱和，磁化强度仅为46×10^-3A·m²/g，在178K出现了超顺磁转变温度，且在测量温度范围内没有发现Verwe y转变. 关键词： 亚铁磁 超顺磁 穆斯堡尔谱     

Deformation of a charge density wave in the vicinity of a point contact with a normal metal

The current-voltage characteristics of Cu-K_0.3MoO₃ point contacts between a metal and a semiconductor with a charge density wave (CDW) are studied for various diameters of the contacts in a wide range of temperatures T and voltages V. In the interval 80 K ? T ? 150 K, the current-voltage characteristics are correctly described in the framework of a semiconductor model: screening of an external electric field causes CDW deformation, shifts the chemical potential of quasiparticles, and changes the point contact resistance. It is shown that the chemical potential is above the middle of the Peierls gap in equilibrium and approaches the middle upon an increase in temperature. The current-voltage characteristics of point contacts with a diameter d ? 100 Å exhibit a sharp decrease in resistance for |V| > V _t , which is associated with the beginning of local CDW sliding within the contact region. The V _t (d, T) dependence can be explained by the size effect in the CDW phase slip.     

The electronic structure of Fe1+xNb3-xSe10

Fe_1+xNb_3-xSe₁₀ has a crystal structure consisting of prismatic niobium chains and iron/niobium octahedral chains. A Charge Density Wave (CDW) has been observed at low temperatures, as might be expected from the similarity of the prismatic niobium chains to those present in NbSe₃. Here we report tight binding band structure calculations which indicate that the electrons responsible for conduction and the CDW reside primarily on the prismatic chains. The effects of disorder and stoichiometry in the iron/niobium octahedral chains on the electronic structure and CDW wave vector are discussed.