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Träfflista för sökning "WFRF:(Mühlbacher Inge) "

Search: WFRF:(Mühlbacher Inge)

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1.
  • Annamalai, Alagappan, et al. (author)
  • Influence of Sb5+ as a Double Donor on Hematite (Fe3+) Photoanodes for Surface-Enhanced Photoelectrochemical Water Oxidation
  • 2018
  • In: ACS Applied Materials and Interfaces. - : American Chemical Society (ACS). - 1944-8244 .- 1944-8252. ; 10:19, s. 16467-16473
  • Journal article (peer-reviewed)abstract
    • To exploit the full potential of hematite (α-Fe2O3) as an efficient photoanode for water oxidation, the redox processes occurring at the Fe2O3/electrolyte interface need to be studied in greater detail. Ex situ doping is an excellent technique to introduce dopants onto the photoanode surface and to modify the photoanode/electrolyte interface. In this context, we selected antimony (Sb5+) as the ex situ dopant because it is an effective electron donor and reduces recombination effects and concurrently utilize the possibility to tuning the surface charge and wettability. In the presence of Sb5+ states in Sb-doped Fe2O3 photoanodes, as confirmed by X-ray photoelectron spectroscopy, we observed a 10-fold increase in carrier concentration (1.1 × 1020 vs 1.3 × 1019 cm–3) and decreased photoanode/electrolyte charge transfer resistance (∼990 vs ∼3700 Ω). Furthermore, a broad range of surface characterization techniques such as Fourier-transform infrared spectroscopy, ζ-potential, and contact angle measurements reveal that changes in the surface hydroxyl groups following the ex situ doping also have an effect on the water splitting capability. Theoretical calculations suggest that Sb5+ can activate multiple Fe3+ ions simultaneously, in addition to increasing the surface charge and enhancing the electron/hole transport properties. To a greater extent, the Sb5+- surface-doped determines the interfacial properties of electrochemical charge transfer, leading to an efficient water oxidation mechanism.
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2.
  • Sandström, Robin, et al. (author)
  • Evaluation of Fluorine and Sulfonic Acid Co-functionalized Graphene Oxide Membranes in Hydrogen Proton Exchange Membrane Fuel Cell Conditions
  • 2019
  • In: Sustainable Energy & Fuels. - : Royal Society of Medicine Press. - 2398-4902. ; 3:7, s. 1790-1798
  • Journal article (peer-reviewed)abstract
    • The use of graphene oxide (GO) based membranes consisting of self-assembled flakes with a lamellar structure represents an intriguing strategy to spatially separate reactants while facilitating proton transport in proton exchange membranes (PEM). Here we chemically modify GO to evaluate the role of fluorine and sulfonic acid groups on the performance of H2/O2 based PEM fuel cells. Mild fluorination is achieved by the presence of hydrogen fluoride during oxidation and subsequent sulfonation resulted in fluorine and SO3- co-functionalized GO. Membrane electrode assembly performance in low temperature and moderate humidity conditions suggested that both functional groups contribute to reduced H2 crossover compared to appropriate reference membranes. Moreover, fluorine groups promoted an enhanced hydrolytic stability while contributing to prevent structural degradation after constant potential experiments whereas sulfonic acid demonstrated a stabilizing effect by preserving proton conductivity.
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