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      Zr and Y co-doped perovskite as a stable, high performance cathode for solid oxide fuel cells operating below 500 °C

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          Abstract

          BaCo 0.4Fe 0.4Zr 0.1Y 0.1O 3−δis applied for the first time as a cathode for low-temperature solid oxide fuel cells (LT-SOFCs) with high power densities below 500 °C and 2500 hours stable performance.

          Abstract

          Zr and Y co-doped perovskite BaCo 0.4Fe 0.4Zr 0.1Y 0.1O 3−δ(BCFZY0.1) was recently developed as a promising new cathode for protonic ceramic fuel cells (PCFCs). Here, it is applied for the first time as a cathode for low-temperature solid oxide fuel cells (LT-SOFCs). It exhibits large lattice parameters, high oxygen reduction reaction (ORR) activity, exceptional low-temperature performance, long-term stability, and excellent chemical compatability with ceria-based SOFC electrolytes. When BCFZY0.1 is used as the cathode in Ce 0.8Gd 0.2O 2−δ(GDC20)-based SOFCs, it enables a peak power density of 0.97 W cm −2at 500 °C with 2500 hours stable performance and complete recoverability without any degradation after more than 80 fast thermal ramping cycles. Even at 350 °C, peak power density reaches 0.13 W cm −2. It also shows good H 2O and CO 2tolerance.

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          Most cited references27

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          A high-performance cathode for the next generation of solid-oxide fuel cells.

          Fuel cells directly and efficiently convert chemical energy to electrical energy. Of the various fuel cell types, solid-oxide fuel cells (SOFCs) combine the benefits of environmentally benign power generation with fuel flexibility. However, the necessity for high operating temperatures (800-1,000 degrees C) has resulted in high costs and materials compatibility challenges. As a consequence, significant effort has been devoted to the development of intermediate-temperature (500-700 degrees C) SOFCs. A key obstacle to reduced-temperature operation of SOFCs is the poor activity of traditional cathode materials for electrochemical reduction of oxygen in this temperature regime. Here we present Ba(0.5)Sr(0.5)Co(0.8)Fe(0.2)O(3-delta)(BSCF) as a new cathode material for reduced-temperature SOFC operation. BSCF, incorporated into a thin-film doped ceria fuel cell, exhibits high power densities (1,010 mW cm(-2) and 402 mW cm(-2) at 600 degrees C and 500 degrees C, respectively) when operated with humidified hydrogen as the fuel and air as the cathode gas. We further demonstrate that BSCF is ideally suited to 'single-chamber' fuel-cell operation, where anode and cathode reactions take place within the same physical chamber. The high power output of BSCF cathodes results from the high rate of oxygen diffusion through the material. By enabling operation at reduced temperatures, BSCF cathodes may result in widespread practical implementation of SOFCs.
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            Readily processed protonic ceramic fuel cells with high performance at low temperatures

            Because of the generally lower activation energy associated with proton conduction in oxides compared to oxygen ion conduction, protonic ceramic fuel cells (PCFCs) should be able to operate at lower temperatures than solid oxide fuel cells (250° to 550°C versus ≥600°C) on hydrogen and hydrocarbon fuels if fabrication challenges and suitable cathodes can be developed. We fabricated the complete sandwich structure of PCFCs directly from raw precursor oxides with only one moderate-temperature processing step through the use of sintering agents such as copper oxide. We also developed a proton-, oxygen-ion-, and electron-hole-conducting PCFC-compatible cathode material, BaCo(0.4)Fe(0.4)Zr(0.1)Y(0.1)O(3-δ) (BCFZY0.1), that greatly improved oxygen reduction reaction kinetics at intermediate to low temperatures. We demonstrated high performance from five different types of PCFC button cells without degradation after 1400 hours. Power densities as high as 455 milliwatts per square centimeter at 500°C on H2 and 142 milliwatts per square centimeter on CH4 were achieved, and operation was possible even at 350°C.
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              Direct oxidation of hydrocarbons in a solid-oxide fuel cell

              Park, Vohs, Gorte (2000)
              The direct electrochemical oxidation of dry hydrocarbon fuels to generate electrical power has the potential to accelerate substantially the use of fuel cells in transportation and distributed-power applications. Most fuel-cell research has involved the use of hydrogen as the fuel, although the practical generation and storage of hydrogen remains an important technological hurdle. Methane has been successfully oxidized electrochemically, but the susceptibility to carbon formation from other hydrocarbons that may be present or poor power densities have prevented the application of this simple fuel in practical applications. Here we report the direct, electrochemical oxidation of various hydrocarbons (methane, ethane, 1-butene, n-butane and toluene) using a solid-oxide fuel cell at 973 and 1,073 K with a composite anode of copper and ceria (or samaria-doped ceria). We demonstrate that the final products of the oxidation are CO2 and water, and that reasonable power densities can be achieved. The observation that a solid-oxide fuel cell can be operated on dry hydrocarbons, including liquid fuels, without reforming, suggests that this type of fuel cell could provide an alternative to hydrogen-based fuel-cell technologies.
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                Author and article information

                Journal
                EESNBY
                Energy & Environmental Science
                Energy Environ. Sci.
                Royal Society of Chemistry (RSC)
                1754-5692
                1754-5706
                2017
                2017
                : 10
                : 1
                : 176-182
                Affiliations
                [1 ]Department of Metallurgical and Materials Engineering
                [2 ]Colorado School of Mines
                [3 ]USA
                [4 ]CoorsTek
                [5 ]Golden
                [6 ]Department of Materials Science and Engineering
                [7 ]Clemson University
                [8 ]Clemson
                Article
                10.1039/C6EE01915C
                fee18e5f-5e50-42b0-a5ef-cdb4ced50d1b
                © 2017
                History

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