Fracture behavior under mixed-mode loading of ceramic plasma-sprayed thermal barrier coatings at ambient and elevated temperatures

The fracture behavior under modes I and II loading of ceramic plasma-sprayed thermal barrier coatings was determined in air at 25 and 1316 °C in asymmetric four-point flexure. The mode I fracture toughness was found to be K_Ic = 1.15 ± 0.07 and 0.98 ± 0.13 MPa , respectively, at 25 and 1316 °C. The respective ‘nominal’ mode II fracture toughness values were K_IIc = 0.73 ± 0.10 and 0.65 ± 0.04 MPa . The empirical mixed-mode fracture criterion best described the coatings’ fracture behavior under mixed-mode loading. The angle of crack propagation was in reasonable agreement with the minimum strain energy density criterion.     

Electric response as a function of applied voltage of Nb-doped Bi4Ti3O12 thin films

We have investigated the electrical properties of sol-gel deposited Nb-doped Bi₄Ti₃O₁₂ (NBIT) ferroelectric thin films. The obtained values of remanent polarization (2P_r) and coercive voltage (V_c) were 7 μC/cm² and 2.5 V of NBIT thin film, respectively. From complex dielectric spectra, we observed the dielectric response consisting of two regions for measuring frequency; the low frequency region may be due to diffusion charge transport caused by impurities, while the dielectric relaxation mechanism of high frequency region seems to be the modified Debye type. A model was proposed to account for the observed phenomena, which fits very well to the dielectric dispersion relation: . The occurrence of an anomaly in n, σ, τ, and ε_S − ε_∞ parameters near V_c indicates a coupling between the charge carriers and ferroelectricity.     

Synthesis of the intermetallic clathrate Na2Ba6Si46 by oxidation of Na2BaSi4 with HCl

A new preparation route to the intermetallic clathrate-I compound Na₂Ba₆Si₄₆ is introduced, which allows one to make large amounts of product with standard laboratory equipment. The precursor Na₂BaSi₄ is oxidized with gaseous HCl at 673 K to Na₂Ba₆Si₄₆, NaCl and BaCl₂. Full-profile refinement of the crystal structure from the X-ray powder diffraction data revealed a composition close to Na₂Ba₆Si₄₆ (Na_1.94(1)Ba_6.06(1)Si₄₆, space group , a=10.281(1) Å). Differential scanning calorimetry showed an exothermic effect at 874 K, indicating that Na₂Ba₆Si₄₆ is metastable. The product was additionally characterized by scanning electron microscopy. The electronic structure of Na₂Ba₆Si₄₆ was investigated by a first-principles, all-electron full-potential method, predicting metallic conductivity. Na₂Ba₆Si₄₆ obtained by oxidation with HCl shows Pauli paramagnetism; no bulk superconductivity was found down to 1.8 K in a magnetic field of 20 Oe.     

Composition dependent thermoelectric properties of sintered Mg2Si1−xGex (x = 0 to 1) initiated from a melt-grown polycrystalline source

Fabrication of Mg₂Si_1−xGe_x (x = 0-1.0) was carried out using a spark plasma sintering technique initiated from melt-grown polycrystalline Mg₂Si_1−xGe_x powder. The thermoelectric properties were evaluated from RT to 873 K. The power factor of Mg₂Si_1−xGe_x with higher Ge content (x = 0.6-1.0) tends to decrease at higher temperatures, and the maximum value of about 2.2 × 10^− 5 Wcm^− 1K^− 2 was observed at 420 K for Mg₂Si and Mg₂Si_0.6Ge_0.4. The coexistence of Si and Ge gave rise to a decrease in the thermal conductivity in the Mg₂Si_1−xGe_x. The values close to 0.02 Wcm^− 1K^− 1 were obtained for Mg₂Si_1−xGe_x (x = 0.4-0.6) over the temperature range from 573 to 773 K, with the minimum value being about 0.018 Wcm^− 1K^− 1 at 773 K for Mg₂Si_0.4Ge_0.6. The maximum dimensionless figure of merit was estimated to be 0.67 at 750 K for samples of Mg₂Si_0.6Ge_0.4.     

Growth of La0.7Sr0.3MnO3 films on Si(0 0 1) using SrMnO3 template layer

Using RF magnetron sputtering, we have successfully grown (1 1 0) orientated La_0.7Sr_0.3MnO₃ (LSMO) films on Si(0 0 1) wafers using SrMnO₃ (SMO) as a template layer. The X-ray diffraction (XRD) patterns of the SMO/Si heterostructures indicate that SMO grows along the (1 1 0) orientation, the orientation relationship between the SMO thin film and the Si (0 0 1) substrate being given by (0 1 1)_SMO∣∣(0 0 1)_Si and [01]_SMO∣∣[0 1 0]_Si. From the XRD patterns of the LSMO/SMO/Si heterostructures, we find that with an increase of substrate temperature, the required thickness of SMO, which plays an effective role of tuning the preferential orientation of LSMO, will decrease at first and then increase. It is thought that this originates from the fact that the crystallization of SMO is not perfect at low temperatures whereas too high a temperature results in reaction and diffusion at the interface of the two layers.     

Synthesis and characterization of a new organic dihydrogenomonophosphate [3,5-(CH3O)2C6H3NH3]2(H2PO4)2

Chemical preparation, crystal structure, calorimetric studies and spectroscopic investigation are given for a new organic cation dihydrogenomonophosphate [3,5-(CH₃O)₂C₆H₃NH₃]₂(H₂PO₄)₂. This compound is triclinic with the following unit cell parameters: a=9.030(6) Å, b=16.124(5) Å, c=8.868(3) Å, α=75.04(3)°, β=110.71(4)°, γ=104.61(1)°, Z=4, V=1148.0(1) Å³, Z=2 and ρ_cal.=1.454 g cm⁻³. Crystal structure was solved and refined to R=0.04, 2752 independent reflections. The atomic arrangement can be described as inorganic layers of H₂PO₄⁻ anions parallel to planes, between which are located the organic groups. Solid-state and MAS-NMR spectroscopies are in agreement with the X-ray structure. Ab initio calculations allow the attribution of the phosphorous and carbon signals to the independent crystallographic sites and to the various atoms of the organic groups.     

Chemical preparation, crystal structure and characterization of the new sodium ytterbium cyclotriphosphate Na3Yb(P3O9)2·9H2O

Chemical preparation and crystal structure are reported for a new lanthanide cyclotriphosphate Na₃Yb(P₃O₉)₂·9H₂O. This salt crystallizes in the trigonal system, space group with the following parameters: a = 30.933(2), c = 12.8282(5) Å. The crystal structure was refined to R₁ = 0.0432 using 1782 reflections with I > 2 σ(I). In the Na₃Yb(P₃O₉)₂·9H₂O structure, the phosphoric ring anions, located around the axis are interconnected by YbO₈ dodecahedra and NaO₆ and NaO₇ polyhedra to build, around the threefold axis, large channels parallel to the c axis. All the nine water molecules in the present arrangement participate in the coordination spheres of the associated cations. The thermogravimetric analysis shows that the removal of these water molecules occurs in three stages between 305 and 736 K.The vibrational study by IR absorption spectroscopy of Na₃Yb(P₃O₉)₂·9H₂O is also reported.