首页> 外文期刊>Journal of the American Ceramic Society >Electrophoretic Deposition of Dense La_(0.8)Sr_(0.2)Ga_(0.8)Mg_(0.0115)Co_(0.085)O_(3-δ) Electrolyte Films from Single-Phase Powders for Intermediate Temperature Solid Oxide Fuel Cells
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Electrophoretic Deposition of Dense La_(0.8)Sr_(0.2)Ga_(0.8)Mg_(0.0115)Co_(0.085)O_(3-δ) Electrolyte Films from Single-Phase Powders for Intermediate Temperature Solid Oxide Fuel Cells

机译:中温固体氧化物燃料电池单相粉末致密La_(0.8)Sr_(0.2)Ga_(0.8)Mg_(0.0115)Co_(0.085)O_(3-δ)电解质膜的电泳沉积

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摘要

La_(0.8)Sr_(0.2)Ga_(0.8)Mg_(0.115)Co_(0.085)O_(3-δ) (LSGMC) powders were prepared by polymeric precursor synthesis, using either polyvi-nyl alcohol (PVA) or citric acid (CA) as complexing agents. The powders were synthesized using different ratios between the complexing agent and the cations dissolved in solution. The obtained polymer gel precursors were dried and calcined at temperatures between 1000° and 1450℃. Single-phase LSGMC powders were obtained at a firing temperature of 1450℃, using PVA and a molar ratio between the hydroxylic groups and the total cations of 3:1. Phase-pure LSGMC powders were used to sinter (1490℃, 2 h) thick pellets. The functional properties of LSGMC pellets were assessed by electrochemical impedance spectroscopy. The electrical conductivity values and the apparent activation energies in different transport regimes were in agreement with literature data. The same LSGMC powders were deposited by electrophoretic deposition (EPD) on a green membrane containing lanthanum-doped ceria (La_(0.4)Ce_(0.6)O_(2-x), LDC), a binder, and carbon powders. The LSGMC/LDC bi-layer obtained by EPD was cofired at 1490℃ for 2 h. A dense and crack-free 8-μm-thick LSGMC film supported on a porous skeleton of LDC was obtained. The combined use of proper powder synthesis and film processing routes has thus proven to be a viable way for manufacturing anode-supported LSGMC films.
机译:La_(0.8)Sr_(0.2)Ga_(0.8)Mg_(0.115)Co_(0.085)O_(3-δ)(LSGMC)粉末是使用聚乙烯醇(PVA)或柠檬酸通过聚合物前体合成制备的( CA)作为络合剂。使用络合剂和溶解在溶液中的阳离子之间的不同比例合成粉末。将获得的聚合物凝胶前体干燥并在1000°至1450℃的温度下煅烧。采用PVA,羟基与总阳离子的摩尔比为3:1,在1450℃的焙烧温度下得到单相LSMGC粉末。用相纯LSGMC粉末烧结(1490℃,2 h)厚的粒料。 LSGMC丸的功能特性通过电化学阻抗谱进行评估。不同传输方式下的电导率值和表观活化能与文献数据一致。相同的LSGMC粉末通过电泳沉积(EPD)沉积在含有镧掺杂的二氧化铈(La_(0.4)Ce_(0.6)O_(2-x),LDC),粘合剂和碳粉的绿色膜上。将EPD制得的LSMGC / LDC双层膜在1490℃下共烧2小时。获得了支撑在LDC多孔骨架上的致密且无裂纹的8μm厚LSGMC膜。因此,结合使用适当的粉末合成和薄膜加工路线是制造阳极支撑LSGMC薄膜的可行方法。

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  • 来源
    《Journal of the American Ceramic Society》 |2009年第9期|1999-2004|共6页
  • 作者单位

    Dipartimento di Scienze e Tecnologie Chimiche. Universita di Roma Tor Vergata, Via della Ricerca Scientifica 1, 00133 Rome, Italy;

    Dipartimento di Scienze e Tecnologie Chimiche. Universita di Roma Tor Vergata, Via della Ricerca Scientifica 1, 00133 Rome, Italy;

    Dipartimento di Scienze e Tecnologie Chimiche. Universita di Roma Tor Vergata, Via della Ricerca Scientifica 1, 00133 Rome, Italy;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
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  • 正文语种 eng
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