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Structural, electrical and electrochemical properties of calcium-doped lanthanum nickelate

机译:钙掺杂镍酸镧的结构,电和电化学性质

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The present work focuses on the structural, thermo-mechanical and electrical properties of La2-xCaxNiO4 + (delta) with different calcium content (x = 0-0.4) and the electrochemical performance of the electrodes on their base in contact with a Ce0.8Sm0.2O1.9 electrolyte. It was shown that the introduction of even a small amount of calcium (x = 0.1) stabilized the crystal structure in the tetragonal syngony across the whole temperature range 25-800 degrees C. Dilatometric study of the compact samples in the entire concentration range of Ca showed no phase transitions up to 800 degrees C The total electrical conductivity, measured by a dc four-probe technique, increased with an increase in calcium content. However, electrochemical activity of the La2-xCaxNiO4 + delta - based electrodes, contrarily, drastically decreased. The polarization resistance R-eta, derived from the impedance spectroscopy data, increased from 0.18 Omega.cm(2) (x = 0) to 1.240 Omega.cm(2) (x = 0.3) at 800 degrees C. The coefficients of oxygen surface exchange (k*) and oxygen tracer diffusion (D*) calculated from the oxygen isotope exchange data for La2NiO4+delta were considerably higher than those for La1.7Ca0.3NiO4+delta (4.54-10(-7) cm.s(-1) and 3.02.10(-8) cm(2).s(-1) (x = 0); 2.91-10(-8) cm.s(-1) and 5.82.10(-10) cm(2).s(-1) (x = 0.3) at 800 degrees C, respectively). It was found that for La1.7Ca0.3NiO4+delta the rate-determining stage of oxygen surface exchange is incorporation of oxygen, while for La2NiO4+delta it is oxygen dissociative adsorption. (C) 2016 Elsevier B.V. All rights reserved.
机译:目前的工作集中在具有不同钙含量(x = 0-0.4)的La2-xCaxNiO4 +(δ)的结构,热机械和电学性质以及与Ce0.8Sm0接触的其基底上电极的电化学性能.2O1.9电解质。结果表明,即使在25-800℃的整个温度范围内,即使少量的钙(x = 0.1)的引入也能稳定四方晶系的晶体结构。在整个Ca浓度范围内对致密样品的膨胀学研究在800°C时无相变。通过直流四探针技术测得的总电导率随钙含量的增加而增加。然而,相反,La2-xCaxNiO4 +基于δ的电极的电化学活性急剧下降。从阻抗光谱数据得出的极化电阻R-eta在800摄氏度下从0.18 Omega.cm(2)(x = 0)增加到1.240 Omega.cm(2)(x = 0.3)。氧的系数根据La2NiO4 +δ的氧同位素交换数据计算的表面交换(k *)和氧示踪扩散(D *)明显高于La1.7Ca0.3NiO4 +δ的表面交换(k *)和氧示踪扩散(D *)(4.54-10(-7)cm.s( -1)和3.02.10(-8)cm(2).s(-1)(x = 0); 2.91-10(-8)cm.s(-1)和5.82.10(-10)cm (2).s(-1)(x = 0.3)分别在800摄氏度下)。发现对于La1.7Ca0.3NiO4 +δ,确定氧表面交换的速率阶段是结合氧,而对于La2NiO4 +δ,则是氧解离吸附。 (C)2016 Elsevier B.V.保留所有权利。

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