24
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Mapping electrochemically driven gas exchange of mixed conducting SrTi 0.7Fe 0.3O 3 − δ and Ce 0.8Gd 0.2O 1.9 thin films by 18O tracer incorporation under reducing atmosphere

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Thermally and electrochemically driven 18O tracer exchange experiments in H 2/H 2 18O atmosphere were performed on SrTi 0.7Fe 0.3O 3 − δ and Ce 0.8Gd 0.2O 2 − δ thin films on single crystalline YSZ substrates. Noble metal current collectors were deposited on both films and electrochemically polarized during the exchange experiment. The resulting tracer distribution was analyzed by spatially resolved secondary ion mass spectrometry. Increased tracer fraction near the current collectors was found under cathodic polarization and decreased tracer fraction under anodic polarization. High cathodic bias leads to enhanced n-type electronic conductivity, which increases the extent of the electrochemically active zone.

          Highlights

          • 18O from tracer marked water was incorporated in SrTi 0.7Fe 0.3O 3–δ and Ce 0.8Gd 0.2O 1.8 thin films.

          • On both MIEC thin films, Pt and Au current collectors were applied beneath the film and ontop, respectively.

          • Cathodic polarization extended the oxygen incorporation zone from the current collector along the free electrode surface.

          Related collections

          Most cited references26

          • Record: found
          • Abstract: found
          • Article: not found

          A redox-stable efficient anode for solid-oxide fuel cells.

          Solid-oxide fuel cells (SOFCs) promise high efficiencies in a range of fuels. Unlike lower temperature variants, carbon monoxide is a fuel rather than a poison, and so hydrocarbon fuels can be used directly, through internal reforming or even direct oxidation. This provides a key entry strategy for fuel-cell technology into the current energy economy. Present development is mainly based on the yttria-stabilized zirconia (YSZ) electrolyte. The most commonly used anode materials are Ni/YSZ cermets, which display excellent catalytic properties for fuel oxidation and good current collection, but do exhibit disadvantages, such as low tolerance to sulphur and carbon deposition when using hydrocarbon fuels, and poor redox cycling causing volume instability. Here, we report a nickel-free SOFC anode, La0.75Sr0.25Cr0.5Mn0.5O3, with comparable electrochemical performance to Ni/YSZ cermets. The electrode polarization resistance approaches 0.2 Omega cm2 at 900 degrees C in 97% H2/3% H2O. Very good performance is achieved for methane oxidation without using excess steam. The anode is stable in both fuel and air conditions, and shows stable electrode performance in methane. Thus both redox stability and operation in low steam hydrocarbons have been demonstrated, overcoming two of the major limitations of the current generation of nickel zirconia cermet SOFC anodes.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Efficient and limiting reactions in aqueous light-induced hydrogen evolution systems using molecular catalysts and quantum dots.

            Hydrogen produced from water and solar energy holds much promise for decreasing the fossil fuel dependence. It has recently been proven that the use of quantum dots as light harvesters in combination with catalysts is a valuable strategy to obtain photogenerated hydrogen. However, the light to hydrogen conversion efficiency of these systems is reported to be lower than 40%. The low conversion efficiency is mainly due to losses occurring at the different interfacial charge-transfer reactions taking place in the multicomponent system during illumination. In this work we have analyzed all the involved reactions in the hydrogen evolution catalysis of a model system composed of CdTe quantum dots, a molecular cobalt catalyst and vitamin C as sacrificial electron donor. The results demonstrate that the electron transfer from the quantum dots to the catalyst occurs fast enough and efficiently (nanosecond time scale), while the back electron transfer and catalysis are much slower (millisecond and microsecond time scales). Further improvements of the photodriven proton reduction should focus on the catalytic rate enhancement, which should be at least in the hundreds of nanoseconds time scale.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              High electrochemical activity of the oxide phase in model ceria-Pt and ceria-Ni composite anodes.

              Fuel cells, and in particular solid-oxide fuel cells (SOFCs), enable high-efficiency conversion of chemical fuels into useful electrical energy and, as such, are expected to play a major role in a sustainable-energy future. A key step in the fuel-cell energy-conversion process is the electro-oxidation of the fuel at the anode. There has been increasing evidence in recent years that the presence of CeO(2)-based oxides (ceria) in the anodes of SOFCs with oxygen-ion-conducting electrolytes significantly lowers the activation overpotential for hydrogen oxidation. Most of these studies, however, employ porous, composite electrode structures with ill-defined geometry and uncontrolled interfacial properties. Accordingly, the means by which electrocatalysis is enhanced has remained unclear. Here we demonstrate unambiguously, through the use of ceria-metal structures with well-defined geometries and interfaces, that the near-equilibrium H(2) oxidation reaction pathway is dominated by electrocatalysis at the oxide/gas interface with minimal contributions from the oxide/metal/gas triple-phase boundaries, even for structures with reaction-site densities approaching those of commercial SOFCs. This insight points towards ceria nanostructuring as a route to enhanced activity, rather than the traditional paradigm of metal-catalyst nanostructuring.
                Bookmark

                Author and article information

                Contributors
                Journal
                Solid State Ion
                Solid State Ion
                Solid State Ionics
                Elsevier Science B.V
                0167-2738
                1872-7689
                1 May 2015
                May 2015
                : 273
                : 25-29
                Affiliations
                Vienna University of Technology, Institute of Chemical Technologies and Analytics, Getreidemarkt 9/164, 1060 Vienna, Austria
                Author notes
                [* ]Corresponding author. alexander.opitz@ 123456tuwien.ac.at
                Article
                S0167-2738(14)00440-8
                10.1016/j.ssi.2014.10.024
                4986286
                3ed529c3-5b3d-463a-b05a-0e7714d9edcc
                © 2014 The Authors. Published by Elsevier B.V.

                This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/).

                History
                : 15 June 2014
                : 16 October 2014
                : 17 October 2014
                Categories
                Article

                thin film electrode,isotopic surface exchange,18o enriched water,electrochemical water splitting,electrochemically active zone

                Comments

                Comment on this article