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Effects of sintering temperature on composition, microstructure and electrochemical performance of spray pyrolysed LSC thin film cathodes

机译:烧结温度对喷雾热解LSC薄膜阴极组成,微观结构和电化学性能的影响

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Thin nanoporous LSC (La_(0.6)Sr_(0.4)CoO_(3-δ)) cathodes are deposited by spray pyrolysis onto gadolinium-doped ceria (GDC) electrolyte substrates, followed by sintering at 600°C, 800°C, and 1000°C. The investigation includes quantitative microstructure analysis, electrochemical characterization and application of Adler-Lane-Steele (ALS) model in order to extract intrinsic material properties and to explain the effects of variation in sintering temperature. A secondary gray phase (SGP) is detected, which consists of Sr and O and has a contrast in backscatter imaging intermediate between the pores and the LSC. SGP fills 66% of the mesopores in LSC sintered at 600 °C. With increasing sintering temperature the amount of SGP decreases until it disappears at 1000 °C. In this investigation we intend to understand the effect of SGP formation. For this purpose the influence of microstructural changes (i.e. active surface area) and variation of intrinsic material properties (exchange flux density) associated with SGP formation need to be quantified. The area specific resistance (ASR) of symmetrical LSC/GDC/LSC cells is measured between 400 and 600°C by impedance spectroscopy. ASR values as low as 0.13 Ω·cm~2 are obtained for samples sintered at 600°C, and 80 times higher for samples sintered at 1000 °C. These results indicate that the SGP is not blocking gas diffusion of O2 in the pores and therefore surface oxygen reduction reaction may take place over the entire LSC surface. Hence at low sintering temperatures a high specific surface area is obtained and the results indicate that formation of SGP does not bring a negative effect neither on the oxygen transport in 1-μm thin electrodes, nor on the oxygen reduction kinetics of LSC. An inverse correlation between the measured ASR values and the LSC-surface is obtained. The exchange neutral flux density, r0, is calculated using the ALS model, which results in r0-values in the range between 10~(-8) (600°C) and 10~(-9) mol/cm~2/s (1000°C). Considering the formation of a secondary SrO-phase in a mass-balance for the entire sample also leads to the conclusion that there must be an increase of A-site deficiency and oxygen vacancies in LSC. In summary, it can be concluded that the variation of the ASR between LSC sintered at 600°C and 1000 °C is more strongly related to the difference in intrinsic material property, (r0 varies by a factor of 40) than the difference in surface area, (a varies by a factor of 2). For a controlled optimization of cathode performance it is necessary to consider all these different aspects (non-stoichiometric compositions, microstructure, secondary phase formation, intrinsic properties, sintering temperature).
机译:通过将热解沉积到钆掺杂的二氧化铈(GDC)电解质基材上沉积薄的纳米多孔LSC(La_(0.6)Sr_(0.4)CoO_(3-Δ))阴极,然后在600℃下烧结,800℃和1000 °C。该研究包括定量微观结构分析,施肥 - 泳钢(ALS)模型的电化学表征和应用,以提取内在材料特性,并解释烧结温度变化的影响。检测次级灰度阶段(SGP),其由SR和O组成,并且在孔和LSC之间的后散射成像中间具有对比度。 SGP填充600℃的LSC中的66%的中孔。随着烧结温度的增加,SGP的量降低,直至其在1000℃下消失。在这项调查中,我们打算了解SGP形成的影响。为此目的,需要量化微观结构变化(即主动表面积)和与SGP形成相关的内在材料特性(交换通量密度)的变化需要量化。对称LSC / GDC / LSC细胞的区域特异性电阻(ASR)通过阻抗光谱测量400-600℃。对于在600℃下烧结的样品获得低至0.13Ω·cm〜2的ASR值,对于1000℃烧结的样品,样品较高的80倍。这些结果表明,SGP未阻断O2在孔中的气体扩散,因此可以在整个LSC表面上进行表面氧还原反应。因此,在低烧结温度下,获得高比表面积,结果表明SGP的形成既不会在1μm薄电极中的氧气输送也不会导致LSC的氧还原动力学。获得测量的ASR值与LSC表面之间的逆相关性。使用ALS型号计算交换中性磁通密度R0,这导致r0值在10〜(-8)(600°C)和10〜(-9)mol / cm〜2 / s之间的r0-值(1000°C)。考虑到整个样品的质量平衡中形成二级阶段的次级阶段也导致了结论,即在LSC中必须增加一个现场缺乏和氧空位。总之,可以得出结论,在600℃和1000℃的LSC之间的ASR之间的变化与内在材料特性的差异更强烈地相关,(R0变化为40倍),而不是表面差异面积,(A变化为2倍)。对于阴极性能的受控优化,需要考虑所有这些不同的方面(非化学计量组合物,微观结构,二次相形成,内在性质,烧结温度)。

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