The non-equilibrium cation site occupancy in nanosized zinc ferrites (6-13 nm) with different degree of inversion (0.2 to 0.4) was investigated using Fe and Zn K-edge x-ray absorption spectroscopy XANES and EXAFS, and magnetic measurements. The very good agreement between experimental and ab-initio calculations on the Zn K-edge XANES region clearly show the large Zntransference that takes place in addition to the well-identified Fe 3+ [B]→Fe 3+ (A) one, without altering the long-range structural order. XANES spectra features as a function of the spinel inversion were shown to depend on the configuration of the ligand shells surrounding the absorbing atom. This XANES approach provides a direct way to sense cationic inversion in these spinel compounds. We also demonstrated that a mechanical crystallization takes place on nanocrystalline spinel that causes an increase of both grain and magnetic sizes and, simultaneously, generates a significant augment of the inversion.

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Differences on carbon content and chemical bonds in a-Si1−xCx:H were observed and analyzed in carbon rich and silicon rich films, deposited by plasma enhanced chemical vapor deposition from mixtures of silane and methane. The influence of the radio frequency low power density regime on the film’s properties was investigated. The content of Si, C, and H in the solid phase was obtained by Rutherford back scattering and forward recoil spectrometry. The bondings were analyzed by Fourier transform infrared spectroscopy. Quantitative analysis on the film’s chemical composition was performed combining the vibrational spectra with the stoichiometry data. The results showed that under “silane starving plasma” conditions, a carbon content as high as 70 at. % is achieved and the main carbon bonds are tetragonal C–H,  C–H2, and Si–C.

In this work we report a study of the magnetic behavior of ferrimagnetic oxide CoFe 2 O 4 treated by mechanical milling with different grinding balls. The cobalt ferrite nanoparticles were prepared using a simple hydrothermal method and annealed at 500 o C. The non-milled sample presented coercivity of about 1.9 kOe, saturation magnetization of 69.5 emu/g, and a remanence ratio of 0.42. After milling, two samples attained coercivity of 4.2 and 4.1 kOe, and saturation magnetization of 67.0 and 71.4 emu/g respectively. The remanence ratio M R /M S for these samples increase to 0.49 and 0.51, respectively. To investigate the influence of the microstructure on the magnetic behavior of these samples, we used X-ray powder diffraction (XPD), transmission electron microscopy (TEM), and vibrating sample magnetometry (VSM). The XPD analysis by the Williamson-Hall plot was used to estimate the average crystallite size and strain induced by mechanical milling in the samples.

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The charge ordering observed in the (TMTTF) 2 X family has been studied by X-ray absorption spectroscopy. XANES measurements at the Sulfur K-edge show no evidence of charge disproportionation larger than 0.5 e, and EXAFS at the Phosphorus K-edge indicate no displacements of the PF 6 anion larger than 0.05 Å. The difficulty to observe a structural signature of this charge ordering is due to the triclinic symmetry of these salts. By contrast, in the monoclinic charge transfer salt (DMtTTF) 2 ClO 4 , a screw axis symmetry constrains the molecular stacks to be uniform. In this real ¼-filled system, charge localization is observed at about 150 K. We show that around this temperature an incommensurate modulation of reduced wave vector (0.58,0,-0.275) is stabilized. The transition is strongly hysteretic, but no long range order is established. We suggest that this modulation, which has the 4k F periodicity in the chain direction, stabilizes a local antiferroelectric state similar to the one previously observed in (TMTTF) 2 SCN.