10 research outputs found

    Three-dimensional Inkjet Printed Solid Oxide Electrochemical Reactors. I. Yttria-stabilized zirconia Electrolyte

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    Solid oxide fuel cell (SOFC) and electrolyser (SOE) performances can be enhanced significantly by increasing the densities of (electrode | electrolyte | pore) triple phase boundaries and improving geometric reproducibility and control over composite electrode | electrolyte microstructures, thereby also aiding predictive performance modelling. We developed stable aqueous colloidal dispersions of yttria-stabilized zirconia (YSZ), a common SOFC electrolyte material, and used them to fabricate 2D planar and highly-customisable 3D microstructures by inkjet printing. The effects of solids fraction, particle size, and binder concentration on structures were investigated, and crack-free, non-porous electrolyte planes were obtained by tailoring particle size and minimising binder concentration. Micro-pillar arrays and square lattices were printed with the optimised ink composition, and a minimum feature size of 35 μm was achieved in sintered structures, the smallest published to-date. YSZ particles were printed and sintered to a 23 μm thick planar electrolyte in a Ni-YSZ|YSZ|YSZ-LSM|LSM electrolyser for CO2 splitting; a feed of 9:1 CO2:CO mixture at 1.5 V and 809 °C produced a current density of −0.78 A cm−2 even without more complex 3D electrode | electrolyte geometries

    Syngas (CO-Hâ‚‚) production using high temperature micro-tubular solid oxide electrolysers

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    AbstractCO2 and/or H2O were reduced to CO/H2 in micro-tubular solid oxide electrolysers with yttria-stabilized zirconia (YSZ) electrolyte, Ni-YSZ cermet cathode and strontium(II)-doped lanthanum manganite (LSM) oxygen-evolving anode. At 822°C, the kinetics of CO2 reduction were slower (ca. −0.49Acm−2 at 1.8V) than H2O reduction or co-reduction of CO2 and H2O, which were comparable (ca. −0.83 to −0.77Acm−2 at 1.8V). Performances were improved (−0.85 and −1.1Acm−2 for CO2 and H2O electrolysis, respectively) by substituting the silver current collector with nickel and avoiding blockage of entrances to pores on the inner lumen of micro-tubes induced by silver paste applied previously to decrease contact losses. The change in current collector materials increased ohmic potential losses due to substituting the lower resistance Ag with Ni wire, but decreased electrode polarization losses by 80–93%. For co-electrolysis of CO2 and H2O, isotopically-labelled C18O2 was used to try to distinguish between direct cathodic reduction of CO2 and its Ni-catalysed chemical reaction with hydrogen from reduction of steam. Unfortunately, oxygen was exchanged between C18O2 and H216O, enriching oxygen-18 in the steam and substituting oxygen-16 in the carbon dioxide, so the anode off-gas isotopic fractions were meaningless. This occurred even in alumina and YSZ tubes without the micro-tubular reactor, i.e. in the absence of Ni catalyst, though not in quartz tubes. Unfortunately, larger differences between the thermal expansion coefficients of quartz and YSZ precluded using a quartz tube to house the micro-tubular reactor. However, the kinetic results, CO/H2 yields from off-gas analysis, diffusional considerations and model predictions of reactant and product gas adsorption on Ni suggested that syngas should be produced by electrochemical reduction of steam to H2, followed by its Ni-catalysed chemical reaction with CO2

    Highly-robust solid oxide fuel cell (SOFC): simultaneous greenhouse gas treatment and clean energy generation

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    Herein, results of combined greenhouse gas treatment with clean energy conversion is reported for the first time. Multi-channel tubular SOFCs were operated with N2O instead of air as the oxidant leading to a 50% increase in power density. Techno-economic evaluation suggested the feasibility of the combined approach eliminating the cost penalty for N2O abatement

    Individual geographic mobility in a Viking-Age emporium—Burial practices and strontium isotope analyses of Ribe’s earliest inhabitants

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    Individual geographic mobility is a key social dynamic of early Viking-Age urbanization in Scandinavia. We present the first comprehensive geographic mobility study of Scandinavia’s earliest emporium, Ribe, which emerged around AD 700 in the North Sea region of Denmark. This article presents the results of strontium isotope analyses of 21 individuals buried at Ribe, combined with an in-depth study of the varied cultural affinities reflected by the burial practices. In order to investigate geographic mobility in early life/childhood, we sampled multiple teeth and/or petrous bone of individuals, which yielded a total of 43 strontium isotope analyses. Most individuals yielded strontium isotope values that fell within a relatively narrow range, between 87Sr/86Sr = 0.709 to 0.711. Only two individuals yielded values >87Sr/86Sr = 0.711. This suggests that most of these individuals had local origins but some had cultural affinities beyond present-day Denmark. Our results raise new questions concerning our understanding of the social and cultural dynamics behind the urbanization of Scandinavia
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