X-ray study of field induced deformation of sliding CDW in K0.30MoO3

A deformation of the CDW is investigated under the electric field whose magnitude is intensionally made inhomogeneous in the one-dimensional conductor K_0.30MoO₃. It is verified that the CDW's deformation, which occurs in the transverse (2a¹-c¹)-direction, is caused by the field gradient in the sample. In the sample where the CDW deformation is found without the intensional inhomogeneity of the electroc field, the deformation is not uniform from point to point. Possible relations are discussed between the structural change and the electrical polarization observed in pulse measurements of the conductivity.     

SrCl2:Co++EPR谱电场效应的理论解释

本文从理论上研究了[111]方向电场对SrCl₂:Co⁺⁺的EPR谱的影响。结果表明:外电场使晶格发生畸变而偏离原来的O_h对称,成为C_3v。由此圆满地从理论上解释了零场分裂因子D随电场强度E线性变化的实验规律,并从理论上预言了晶格在平行电场方向的变化率为α=—8×10^-5α₀mm/kV,在垂直电场方向的变化率β=1.66×10^-4α₀关键词：     

NMR study of KCuF3 at low temperatures

The NMR of F¹⁹ nuclei in KCuF₃ has been measured in the a-type single crystal at 1.7 K. Two types of magnetic domains exist; one occupies most part of the crystal and has easy axis along <110>, and the other occupies the rest of the crystal and has easy axis along <100>. In both domains the moment directions are distributed around the easy axes over a considerable angular range. The spin-flop begins with nearly zero applied field in the <110>;-domain. When the magnetic field is rotated in the c-plane, an angular dependence has been observed for those F¹⁹ nuclei which lie on the c-axis. This dependence arises from the alternate stacking of the ground state wave functions of Cu²⁺ ions.     

Evolution of the spin-density wave-superconductivity texture in the organic superconductor (TMTSF)2PF6 under pressure

We report an investigation at the endpoint region of the spin density wave state in (TMTSF)₂PF₆ where metal and superconductivity emerge. Thanks to resistivity measurements along the three main crystallographic directions, we are able to follow the texture in this phase coexistence regime. In this respect, superconductivity is used as a decoration technique of the metallic pattern. We show that metal (superconductivity) emerges first along the c^? direction in a counterintuitive manner. Then metal (superconductivity) domains evolves from filaments along the c^? axis towards slabs perpendicular to the a-axis which melt together in the homogeneous phase at high pressure. This evolution is compatible with the proposition of the formation of a soliton phase in the vicinity of the critical pressure of the (TMTSF)₂PF₆ phase diagram.     

Giant magnetocaloric effect in the Gd5Ge2.025Si1.925In0.05 compound

The magnetocaloric properties of the Gd 5 Ge 2.025 Si 1.925 In 0.05 compound have been studied by x-ray diffraction,magnetic and heat capacity measurements.Powder x-ray diffraction measurement shows that the compound has a dominant phase of monoclinic Gd5Ge2Si2-type structure and a small quantity of Gd 5(Ge,Si) 3-type phase at room temperature.At about 270 K,this compound shows a first order phase transition.The isothermal magnetic entropy change(△SM) is calculated from the temperature and magnetic field dependences of the magnetization and the temperature dependence of MCE in terms of adiabatic temperature change(△Tad) is calculated from the isothermal magnetic entropy change and the temperature variation in zero-field heat-capacity data.The maximum S M is 13.6 J·kg-1·K-1 and maximum △Tad is 13 K for the magnetic field change of 0-5 T.The Debye temperature(θD) of this compound is 149 K and the value of DOS at the Fermi level is 1.6 states/eV·atom from the low temperature zero-field heat-capacity data.A considerable isothermal magnetic entropy change and adiabatic temperature change under a field change of 0-5 T jointly make the Gd5Ge2.025Si1.925 In 0.05 compound an attractive candidate for a magnetic refrigerant.     

Determination of the electric dipole moment of the HSO radical in its X̃2A″(000) and Ã2A′(003) electronic states

Stark shifts were measured for the zero-field-allowed 0₀₀-1₁₀, 1₁₀-0₀₀ and zero-field-forbidden 0₀₀-1₁₁, 1₁₁-0₀₀ lines of the HSO $\text{A}\text{?}{}^2\text{A′(003)-}\text{X}\text{?}{}^2\text{A″(000)}$ transition. A single-mode dye laser is used to record the Doppler-limited fluorescence excitation spectrum as a function of applied electric field (0–11 kV/cm) for excitation polarizations parallel and perpendicular to the applied field direction. The electric dipole moment along the a axis of this near-prolate asymmetric top is determined to be μ″_a = 2.20 ± 0.08 D and μ′_a = 1.05 ± 0.08 D, in close agreement with recent ab initio calculations.     

Spontaneous magnetostriction of Y2Fe16Al compound

The structure and magnetic properties of Y₂Fe₁₆Al compound have been investigated by means of x-ray diffraction and magnetization measurements. The Y₂Fe Fe₁₆Al compound has a hexagonal Th$_{2}$Ni$_{17}$-type structure. Negative thermal expansion was found in Y₂Fe₁₆Al compound in the temperature range from 332 to 438K by x-ray dilatometry. The coefficient of the average thermal expansion is \alpha =-3.4\times 10^-5K^-1. The spontaneous magnetostrictive deformations from 293 to 427K have been calculated based on the differences between the experimental values of the lattice parameters and the corresponding values extrapolated from the paramagnetic range. The result shows that the spontaneous volume magnetostrictive deformation \textit{$\omega $}$_{\rm S}$ decreases from 5.4$\times $10^-3to near zero with temperature increasing from 293 to 427K, the spontaneous linear magnetostrictive deformation \textit{$\lambda $}$_{\rm c}$ along the $c$ axis is much larger than the spontaneous linear magnetostrictive deformation \textit{$\lambda $}$_{\rm a}$ in basal-plane in the same temperature range except near 427K.     

Thermal expansion of lT-TaS2 and 2H-NbSe2

The thermal expansion of the a and c axes of lT-TaS₂ and of the a axis of 2H-NbSe₂ have been measured between 4 K and 360 K. Discontinuities in the lattice parameters of TaS₂ were observed at the known charge density wave phase transitions near 200 K and 352 K, and a new transition was found near 283 K. These results are used to estimate the entropy changes occurring at the phase transitions. At the charge density wave onset temperature in NbSe₂ we find an upper limit to any discontinuity in the a axis of 2 × 10^-7 and to any discontinuity in the expansion coefficient of 3 × 10^-7 K^-1.     

Neutron diffraction determination of the magnetic structures of NpCo2Si2 and NpCu2Si2

A small polycrystalline ingot sample of NpCo₂Si₂ (weight ≈ 1.5 g) has been studied by neutron diffration between 2 and 160 K on the multi-detector D1B of ILL, Grenoble. At 100 K, the crystal structure is body-centered tetragonal (space group 14/mmm) with a = 3.886 Å and c =9.649 Å. Below T_N = (44 ± 2) K, seven superlattice lines are observed which correspond to a simple tetragonal lattice with lattice constants as above. They are consistent with a type I antiferromagnetic structure of the Np (2a) sublattice, with (001) ferromagnetic sheets coupled antiferromagnetically according to the sequence +-+-. At 6 K, the neptunium moment obtained from the diffracted intensities is: (1.48 ± 0.20)_μuB, and makes an angle 52° ± 15° with the c axis. The cobalt moment is certainly smallet than 0.3_μuB. The Np moment correlates well with the ²³⁷Np hyperfine field deduced from Mos?sbauer spectroscopy; the sublattice magnetization-temoperature curve follows very well the $\text{J=}\text{1}\text{2}$ brillouin curve. The magnetism is therefore probably of lovalized character in this compound. An isomorphous sample of NpCu₂Si₂ (a = 3.990 Å c = 9.920 Å) was shown to be ferromagnetic below (41 ± 2) K, with the Np moment [1.5 ± 0.2)_μuB] aligned along the c axis.     

EPR study of Mn2+ around the ferroelastic transition point of Pb3(PO4)2

The spin Hamiltonian parameters of Mn²⁺ have been measured above and below the transition point (180°C) of the lead phosphate. They show that Mn²⁺ substitutes a Pb_I ion. Between 175 and 180°C the principal axis OX of the fine tensor is parallel to the wave vector of the soft mode which condensates at the transition point. An exaltation of the linewidth is observed. The linewidth remains constant within 5°C of T_c; in this temperature range, the “static regime” is achieved, and the correlation time of the fluctuations is less than 10^?8 sec.     

Fabrication and characterization of GaN/amorphous Ga2O3 nanocables through thermal oxidation

In an effort to obtain one-dimensional core/shell nanostructures, thermal oxidation behavior of GaN nanowires in O₂ with N₂ ambients was investigated by x-ray diffraction, transmission electron microscopy, and x-ray photoelectron spectroscopy. Crystallinity and chemical bonding states of the oxidized surface in the GaN nanowires were strongly dependent on the oxidation temperature. Chemical oxidation reaction occurred upon increasing the temperature, accompanied by the formation of an amorphous Ga₂O₃ layer at the GaN nanowire surface at 900 ^°C. The XPS analyses provided further evidence supporting the change in the chemical bonding states with increasing oxidation temperature.     

One-dimensional electronic order in underdoped surface of YBa2Cu3Oy studied by STM

We have performed low-temperature scanning tunneling microscopy (STM) experiments on the cold-cleaved surface of YBa₂Cu₃O_y single crystals to study the nanoscale electronic order in high-T_c superconductors. STM images measured at low-bias voltage below ∼50 meV show the one-dimensional (1D) electronic modulation along the Cu-O bonds (parallel to the b-axis). The 1D electronic modulation does not have long-range order and the periodicity along the a-axis varies within the range ∼2a-4a depending on the position on the surface, indicating the glassy electronic order in the underdoped CuO₂ plane.     

The infrared spectra of 12C32S, 12C34S, 13C32S,and 12C33S

Using a tunable diode laser spectrometer, the infrared absorption spectra of four isotopic species of carbon monosulfide have been observed in the positive column of a dc discharge of CS₂ and Ar. The wavenumbers of 115 vibration-rotation transitions between 1180.5 and 1266.1 cm^?1 have been measured. These lines were assigned to the 1-0, 2-1, 3-2, and 4-3 bands of ¹²C³²S, the 1-0 and 2-1 bands of ¹²C³⁴S and ¹³C³²S, and the 1-0 band of ¹²C³³S. These new data have been combined with the previous infrared and microwave results to determine Dunham coefficients (Y_ij), the Dunham potential expansion constants (a₀,a₁,a₂,a₃, and a₄), and the classical turning points by the RKR method.     

Magnetic phase transitions and structures of Co3V 2O8

Co₃V ₂O₈ is a spin- 3/2 system on a Kagomé staircase and is known to undergo two magnetic phase transitions between 6 and 11 K. The H-T phase diagram of Co₃V ₂O₈ derived by magnetization measurements on a single crystal is presented. Additionally both ordered magnetic structures were investigated by neutron powder diffraction experiments and solved using Bertaut’s macroscopic theory. For the ferromagnetic phase the magnetic moments of the Co²⁺ ions were found to be 1.5(3)μ_B and 2.7(1)μ_B at 3.5 K along the crystallographic a axis for the (4a) and (8e) sites, respectively. The antiferromagnetic phase exhibits a magnetic cell with a doubled b axis with respect to the nuclear one. The magnetic moments point along the a axis being 1.8(2)μ_B (4a) and 1.8(1)μ_B (8e) at 8 K.     

The antiferromagnetic structures of TbCu2Ge2 and HoCu2Ge2 by neutron diffraction

The magnetic structures of TbCu₂Ge₂ and HoCu₂Ge₂ were studied by neutron diffraction. At 293 K the chemical structure is tetragonal body centered, space group I 4/mmm. The magnetic cell at 4.2 K is four times larger than the chemical one with a wave vector $\text{k =}\text{1}\text{2}\text{0}\text{1}\text{2}$. The magnetic space group is triclinic P_a$\text{1}$(Sh₂⁷) for both compounds. The moment values and directions are μ_Tb = 8.48(6) [μ_B] along [110] tetr. and μ_HO = 6.5(1)[μ_B] making an angle of 81.4(°) with c and 80(°) with a₁. The structure consists of ferromagnetic (101) layers stacked antiferromagnetically.     

Determination de la structure magnetique de la phase Na5Fe3F14γ

The magnetic structure of the ferrimagnetic fluoride - Na₅Fe₃F₁₄ has been determined. The magnetic moments of the iron atoms in (2a) and (4d) sites are antiparallel and directed along the c axis. The magnetic group is P4₂2′₁2′.     

Surface anisotropy of CrxN1−x films prepared on an inner wall by magnetic sputtering

The Cr_xN_1−x films were prepared by magnetic sputtering on an inner wall of a column. Their surface morphologies were studied by atomic force microscopy (AFM) and found to be anisotropic. The 3-D AFM images indicate the grains grow upward along the rotational axis of the system. The AFM top views show a mosaic-like pattern for all samples. Analysis of the height-height correlation function demonstrates that correlation length along the rotational axis of the system is longer than that vertical to the axis. The correlation length and RMS roughness increase with the flow rate of N₂. A deposition model proposed that the shadowing effect of the reactive gas N₂ is the dominant factor for surface anisotropy. The bias added on the substrate is regarded to modulate the grain direction to the rotation axis and enhance roughness and defects.     

Electron paramagnetic resonance in the system CaO-SiO2-Al2O3 containing sulfur

An EPR absorption was detected in the system CaO-SiO₂-Al₂O₃ doped with sulfur. The signal consisted of six isotropic hyperfine lines and demonstrated isotropic fine structure and forbidden doublets. The signal was attributed to an Mn²⁺ impurity displacing Ca²⁺ in fine CaS crystallites formed in the matrix of the ternary system. The spectrum was well accounted for with the parameters g = 2.0021 ± 0.0001 and A = ?77.1 ± 0.6 × 10^?4 cm^?1. Sample preparation conditions did not affect the hyperfine splitting, although the fine structure and forbidden lines proved to be dependent on the conditions of preparation. It is suggested that the appearance of the fine structure is a result of the second effect of the hyperfine structure when the cubic field parameter a approaches zero and, consequently, the structure is free of superposition caused by an anisotropic shift determined by a. We ascribe the change in fine structure to the variation in a and discuss the nature of the energy splitting of the ${}^6\text{S}{}_{\mathrm{<mtext>5</mtext><mtext>2</mtext>}}$ state in a cubic field. We also note a correlation between the fine structure and the forbidden lines. This finding suggests that a is not necessarily specific to the host lattice and, furthermore, that the consideration of superposition of axial or lower symmetry upon the original cubic field of the central Mn²⁺ ion is vital for the determination of a.     

Infrared spectra and lattice vibrations of the spin-chain compound LiCuVO 4

The infrared spectra of the one-dimensional antiferromagnet LiCuVO₄ are measured in the frequency range from 10 cm^-1 to 10 000 cm^-1 and at temperatures from 2 K to 300 K, for the electric field vector E of the radiation polarized either along the a- or along the b-crystallographic directions. For each polarization six infrared active phonon modes are observed in accordance with factor group analysis of the crystal structure of LiCuVO₄. The theoretical group analysis of the possible spinel low-symmetry phases is performed within the framework of Landau's theory of phase transitions. The parameters of several phonon lines show noticeable anomalies around 150 K where the magnetic correlations appear in the copper chains, which may indicate a finite interaction between the phonon and the magnon subsystems in LiCuVO₄. Received 19 February 2001 and Received in final form 26 June 2001     

EPR study of the T2+ center in the paraelectric and antiferroelectric phases of NH4H2PO4

The EPR T

²⁺ center in NH₄H₂PO₄ was studied in the range of temperature 85K – 175K which includes the antiferroelectric transition. The center has the symmetry of NH⁺₄ site, where it goes substitutionally, in both the paraelectric and antiferroelectric phases. In the antiferr$\text{o}$electric phase there is a charge compensations mechanism involving the repulsion of one of the neighbor protons in the hydrogen bond. A measurement of the splitting of the resonance lines for the field along the cristallographic direction $\text{a}$ is presented as a function of temperature. This splitting is proportional to the order parameter.