A series of (Zn,Co)O layers with Co contents x up to 40% grown by atomic layer deposition have been investigated. All structures deposited at 160 • C show magnetic properties specific to II-VI dilute magnetic semiconductors with localized spins S = 3/2 coupled by strong but short-range antiferromagnetic interactions resulting in low-temperature spin-glass freezing for x = 0.16 and 0.4. At higher growth temperature (200 • C) metallic Co nanocrystals precipitate in two locations giving rise to two different magnetic responses: (i) a superparamagnetic contribution coming from volume disperse nanocrystals; (ii) a ferromagneticlike behavior brought about by nanocrystals residing at the (Zn,Co)O/substrate interface. It is shown that the dipolar coupling within the interfacial two-dimensional dense dispersion of nanocrystals is responsible for the ferromagneticlike behavior.

SummaryZinc oxide nanopowders doped with 1–15 mol % cobalt were produced by the microwave solvothermal synthesis (MSS) technique. The obtained nanoparticles were annealed at 800 °C in nitrogen (99.999%) and in synthetic air. The material nanostructure was investigated by means of the following techniques: X-ray diffraction (XRD), helium pycnometry density, specific surface area (SSA), inductively coupled plasma optical emission spectrometry (ICP-OES), extended X-ray absorption fine structure (EXAFS) spectroscopy, scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS) and with magnetometry using superconducting quantum interference device (SQUID). Irrespective of the Co content, nanoparticles in their initial state present a similar morphology. They are composed of loosely agglomerated spherical particles with wurtzite-type crystal structure with crystallites of a mean size of 30 nm. Annealing to temperatures of up to 800 °C induced the growth of crystallites up to a maximum of 2 μm in diameter. For samples annealed in high purity nitrogen, the precipitation of metallic α-Co was detected for a Co content of 5 mol % or more. For samples annealed in synthetic air, no change of phase structure was detected, except for precipitation of Co3O4 for a Co content of 15 mol %. The results of the magentometry investigation indicated that all as-synthesized samples displayed paramagnetic properties with a contribution of anti-ferromagnetic coupling of Co–Co pairs. After annealing in synthetic air, the samples remained paramagnetic and samples annealed under nitrogen flow showed a magnetic response under the influences of a magnetic field, likely related to the precipitation of metallic Co in nanoparticles.

The Xe 5s nondipole photoelectron parameter is obtained experimentally and theoretically from threshold to 200 eV photon energy. Significant nondipole effects are seen even in the threshold region of this valence shell photoionization. In addition, contrary to previous understanding, clear evidence of interchannel coupling among quadrupole photoionization channels is found. DOI: 10.1103/PhysRevLett.91.053002 PACS numbers: 31.25.Eb, 32.80.Fb Until recently, conventional wisdom had assumed nondipole effects in photoionization were negligible at relatively low photon energies, perhaps for energies up to a few keV, but certainly for photon energies below a few hundred eV [1][2][3]. Indeed, despite indications to the contrary [4 -7], the usual practice in the field of photoionization, particularly for experiment, had been to ignore effects beyond the dipole approximation for photon energies as high as several keV. While this may be a reasonable assumption for integrated cross sections, recent work has shown it is certainly wrong for differential cross sections (i.e., photoelectron angular distributions). Experiments have shown the importance of nondipole effects in the 1-3 keV photon-energy region [8,9], in the hundreds-of-eV range [10], and, in one case, at 13 eV [11]. Concurrently, theory has predicted significant nondipole contributions to electron angular distributions for atomic valence shells down to threshold at a few tens of eV photon energy [12 -14].In addition, for dipole photoionization, interchannel coupling, which is simply configuration interaction in the continuum, has been shown to be important for most subshells of most atoms at most energies [15,16]; this work was contrary to the previous conventional wisdom that the independent-particle approximation (IPA) was generally valid away from thresholds. It had been suggested, however, that such interchannel coupling was not important in quadrupole photoionization channels [17], but recent theory has suggested that interchannel coupling can indeed be significant in quadrupole photoionization channels as well [14].To test these two ideas, significant nondipole contributions to the photoionization of a valence shell in the threshold region, and the existence of interchannel coupling effects in quadrupole photoionization channels, we have performed a benchmark experiment on the differential photoionization cross section of Xe 5s from 26 eV (close to threshold) to 200 eV to obtain the nondipole contribution to the photoelectron angular distribution which arises from interference between dipole (E1) and quadrupole (E2) channels. The differential cross section is given by [6,[18][19][20] where is the angle-integrated cross section, is the dipole anisotropy parameter, P 2 cos 3cos 2 ÿ 1=2, and and are nondipole asymmetry parameters. The coordinate axes have the positive x axis along the direction of the photon propagation vector, the z axis along the photon polarization vector, and and are the polar and azimuthal angles of the photoelectron momentum vector. ...

Flexible polyurethane foams (FPF) are polymer materials that have high flammability. Fyrol PNX (FPNX) and expandable graphite (EG), have been used to modify the properties of these materials. The aim of this study was to assess the possibility of improving the thermal stability and flame retardancy of FPF by the addition of FPNX and EG fillers. The prepared foams were characterised by their apparent density, hardness, flexibility, irreversible strain and linear flammability, as well as thermogravimetric analysis (TGA), dynamic mechanical analysis, Fourier transform infrared spectroscopy (FT-IR) and pyrolysis combustion flow calorimetry (PCFC) measurements. The apparent density, hardness, flexibility and irreversible strain results showed that the addition of graphite and phosphorous fillers to the FPF makes slight changes to the mechanical properties, which remain within the acceptable norms. It was also observed that reducing the amount of Fyrol PNX and replacing it with the same amount of EG allowed similar values of linear flammability to be obtained with a simultaneous increase in thermal stability, as shown in the TGA study and the PCFC test. Moreover, it was found that the modification of flexible polyurethane foam by the addition of a mixture of FPNX and EG fillers allows the best properties of this type of materials to be obtained. This result indicates that this type of modification could be an effective way to improve the thermal stability of FPF.

The local order around Mn atoms in the Mn-implanted Si samples, with ferromagnetic properties, has been investigated by use of x-ray-absorption spectroscopy techniques. Analysis of both extended x-ray-absorption fine structure and x-ray absorption near-edge structure spectra clearly indicates that Mn ions are located neither in the substitutional nor in the interstitial position in the Si lattice, but depending on how the samples were prepared, they have five to eight near neighbors.

The x-ray absorption near edge structure (XANES) of selenium is investigated in the crystals with compositions from the pseudobinary cut line Cu2Se-In2Se3. This includes CuInSe2, indium-rich ternary compounds (Cu2In4Se7, CuIn3Se5, CuIn5Se8, CuIn7Se11) and α-In2Se3. The absorption at the K and L3/L2 edges of selenium has been measured using synchrotron radiation. Two theoretical approaches are used to the interpretation of the experimental data: the band structure calculation and the real-space multiple-scattering (RSMS) method. In the first one, the angular momentum projected densities of states at Se sites are calculated for CuInSe2 and α-In2Se3 for the energies up to 17 eV above the conduction band minimum by the LMTO-ASA method. The RSMS approach represented by the FEFF8 code is used to calculate the XANES spectra for the phases with tetragonal symmetry. Clusters up to 160 atoms are used in the calculations. The influence of different structural factors on the selenium XANES is studied.

Changes of the local structure around Mn atoms in (Ga, Mn)As layers after high temperature annealing were determined by x-ray absorption spectroscopy (EXAFS) and high-resolution x-ray diffraction (HRXRD) measurements, and related to their magnetic properties. X-ray absorption is known to be able to detect crystalline structure changes occurring around investigated atoms. The qualitative and quantitative analysis of EXAFS spectra gives unambiguous evidence for the transition from a cubic to a hexagonal phase around Mn atoms as a result of annealing at temperatures of 500 and 600• C. The performed HRXRD investigation indicated a relaxation of the GaAs matrix during annealing, from highly to slightly compressively strained, and finally, after the formation of inclusions of hexagonal MnAs, to slightly tensile strained. The sample with hexagonal MnAs inclusions exhibits ferromagnetic properties up to room temperature with almost all Mn atoms being in a ferromagnetic phase.

The local atomic structure around the central iron of the synthetic soluble analog of malarial pigment in acetic acid solution and with addition of chloroquine as found by X-ray absorption spectroscopy is reported. The special interest was drawn to the axial linkage between the central iron atom of the ferriprotoporphyrin IX (FePPIX) coordinated axially to the propionate group of the adjacent FePPIX. This kind of bonding is typical for hematin anhydride. Detailed analysis revealed differences in oxygen coordination sphere (part of dimer linkage bond) between synthetic equivalent of hemozoin in the powder state and dissolved in acetic acid and water at different concentrations mimicking the physiological condition of the parasite's food vacuole. The results of performed studies suggest that the molecular structure of synthetic analogue of hemozoin is no longer dimer-like in acidic solution. Further changes in atomic order around Fe are seen after addition of the antimalarial drug chloroquine.