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  • 1.
    Cordoba Gallego, Jose Manuel
    et al.
    Linköping University, Department of Physics, Chemistry and Biology, Nanostructured Materials . Linköping University, The Institute of Technology.
    Ballem, Mohamed
    Linköping University, Department of Physics, Chemistry and Biology, Nanostructured Materials . Linköping University, The Institute of Technology.
    Johansson, Emma
    Linköping University, Department of Physics, Chemistry and Biology, Nanostructured Materials . Linköping University, The Institute of Technology.
    Odén, Magnus
    Linköping University, Department of Physics, Chemistry and Biology, Nanostructured Materials . Linköping University, The Institute of Technology.
    Growth of single crystalline dendritic Li(2)SiO(3) arrays from LiNO(3) and mesoporous SiO(2)2011In: Journal of Solid State Chemistry, ISSN 0022-4596, E-ISSN 1095-726X, Vol. 184, no 7, p. 1735-1739Article in journal (Refereed)
    Abstract [en]

    A solution based wet chemistry approach has been developed for synthesizing Li(2)SiO(3) using LiNO(3) and mesoporous silica as starting materials at 550 degrees C. A reaction path where NO and O(2) are formed as side-products is proposed. The crystals synthesized exhibit dendritic growth where the as-prepared nanodendrite is a typical 1-fold nanodendrite composed of one several microns long and some tenth of nanometers wide trunk with small branches, which are several hundreds of nanometers long and up to 70 nm in diameter. The effect of the structure of the mesoporous silica for the final morphology is discussed.

  • 2.
    Grins, Jekabs
    et al.
    Stockholm University.
    Käll, Per-Olov
    Stockholm University.
    Svensson, Gunnar
    Stockholm University.
    Synthesis, structure and magnetic susceptibility of the oxynitride spinell Mn2(MnTa3)N6-δO2+δ, 0≤δ≤11995In: Journal of Solid State Chemistry, ISSN 0022-4596, E-ISSN 1095-726X, Vol. 117, no 1, p. 48-54Article in journal (Refereed)
    Abstract [en]

    The oxynitride spinel Mn2(MnTa3)N6-δO2+δ, with 0 ≤ δ ≤ 1, has been synthesized at 1175 K by ammonolysis of a mixture of a Ta-containing xerogel and Mn(OAc)2 · 4H2O. The N content was determined by combustion analysis and thermogravimetric oxidation, yielding a composition confined between Mn2(MnTa3)N6O2 (δ = 0) and Mn2(MnTa3)N5O3 (δ = 1). The structure is cubic, with space group Fd3m and a = 8.8353(3) Å. It was refined using the Rietveld technique and neutron powder diffraction data collected at room temperature and 15 K, to RF = 2.9 and 3.8%, respectively. The tetrahedral sites are occupied only by Mn atoms and the octahedral sites statistically by 25% Mn and 75% Ta atoms. The N and O atoms are randomly distributed over the anion sites. The magnetic susceptibility exhibits a maximum at 29 K and a Curie-Weiss behavior at higher temperatures with θa = -250(20) K and μeff = 5.7(2) Bohr magnetons per Mn atom. The neutron powder diffraction data collected at 15 K showed no evidence of magnetic ordering. A NaCl-type phase with a = 4.4382(2) Å and tentative composition Mn0.8Ta0.2(O,N) was observed in preparations at 1175 K. A hexagonal Mn4Ta2(O,N)x phase with cell dimensions a = 5.3024(4) Å, c = 14.493(2) Å was obtained at 973 K.

  • 3.
    Mustafa, Elfatih
    et al.
    Linköping University, Department of Science and Technology, Physics and Electronics. Linköping University, Faculty of Science & Engineering.
    Tahira, Aneela
    Linköping University, Department of Science and Technology, Physics and Electronics. Linköping University, Faculty of Science & Engineering.
    Adam, Rania Elhadi
    Linköping University, Department of Science and Technology, Physics and Electronics. Linköping University, Faculty of Science & Engineering.
    Ibupoto, Zafar Hussain
    Institute of Chemistry, University of Sindh, 76080, Jamshoro, Pakistan.
    Elhag, Sami
    Linköping University, Department of Science and Technology, Physics and Electronics. Linköping University, Faculty of Science & Engineering.
    Willander, Magnus
    Linköping University, Department of Science and Technology, Physics and Electronics. Linköping University, Faculty of Science & Engineering.
    Nur, Omer
    Linköping University, Department of Science and Technology, Physics and Electronics. Linköping University, Faculty of Science & Engineering.
    Efficient Ni–Fe layered double hydroxides/ZnO nanostructures for photochemical water splitting2019In: Journal of Solid State Chemistry, ISSN 0022-4596, E-ISSN 1095-726X, Vol. 273, p. 186-191Article in journal (Refereed)
    Abstract [en]

    Zinc oxide (ZnO) nanostructures are widely investigated for photocatalytic applications but the functional properties are limited by the fast carrier recombination rate, which is an intrinsic property of ZnO. To optimize the recombination rate of ZnO, a study is carried out in which it is covered with Ni-Fe layered double hydroxides and synergistic effects are created which boosted the photocatalytic activity of ZnO. The nanostructured materials are synthesized by the low temperature aqueous chemical growth and electrodeposition methods. These nanostructures are characterized by scanning electron microscopy (SEM) and powder X-ray diffraction (XRD) technique. SEM study has revealed a Ni–Fe LDH coated ZnO NRs. The powder XRD has showed a cubic phase of the Ni-Fe layered double hydroxide on the ZnO NRs having an excellent crystalline quality. The optical characterization has shown low scattering of light for the Ni–Fe LDH coated ZnO NRs sample. The sample prepared with deposition time of 25 s showed excellent photochemical water splitting properties compared to counter photo-anodes in alkaline media. The photo response was highly stable and fast. The incident photon to current conversion efficiency for the photo-anode of Ni–Fe(LDHs)/ZnO over 25 s was 82% at a maximum absorption of 380 nm compared to the pristine ZnO NRs which has 70% at the same wavelength. This study is providing a simple, cost effective, earth abundant and environment friendly methodology for the fabrication of photo-anodes for diverse applications specifically water oxidation and solar radiation driven water splitting.

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