首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Electrochemical Impedance Spectroscopy of High-Efficiency Hydrogen Membrane Fuel Cells Based on Sputter-Deposited BaCe0.8Y0.2O3-delta Thin Films
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Electrochemical Impedance Spectroscopy of High-Efficiency Hydrogen Membrane Fuel Cells Based on Sputter-Deposited BaCe0.8Y0.2O3-delta Thin Films

机译:基于溅射沉积BaCe0.8Y0.2O3-δ薄膜的高效氢膜燃料电池的电化学阻抗谱

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摘要

A hydrogen membrane fuel cell (HMFC) consisting of a Pd solid anode, 1 mu m thick BaCe0.8Y0.2O3-delta thin-film electrolyte, and La0.6Sr0.4Co0.2Fe0.8O3 cathode was examined. A single-phase BaCe0.8Y0.2O3-delta thin film was successfully deposited by radio frequency cosputtering with BaCe0.8Y0.2O3 and Ce0.9Y0.1O2 double targets, as checked by X-ray diffraction, transmission electron microscopy, and wavelength dispersive X-ray analysis. The maximum power density reached 1.05 W cm-(2) at 600 degrees C, and this value was higher than the champion data of the recently reported proton-conducting ceramic fuel cells (PCFCs). Electrochemical impedance analysis was performed to characterize the anode and cathode polarization behavior. The impedance responses of HMFC were explicable with an equivalent circuit built by a series connection of cathode charge-transfer elements and anode mass-transfer elements. The contribution of the mass transfer in Pd bulk was found to be relatively small in comparison to cathode polarization and ohmic loss in normal fuel cell atmosphere. Moreover, the cathodic charge-transfer resistance of HMFC was found to be 25 times smaller than those of the recent PCFC systems. The current results demonstrated that the HMFC retained relatively large gas-proton-electron triple-boundary zones near the interface between the BaCe0.8Y0.2O3-delta electrolyte and porous La0.6Sr0.4Co0.2Fe0.8O3-delta cathode.
机译:研究了由Pd固体阳极,1μm厚的BaCe0.8Y0.2O3-δ薄膜电解质和La0.6Sr0.4Co0.2Fe0.8O3阴极组成的氢膜燃料电池(HMFC)。通过X射线衍射,透射电子显微镜和波长色散检查,通过与BaCe0.8Y0.2O3和Ce0.9Y0.1O2双靶射频共溅射成功地沉积了单相BaCe0.8Y0.2O3-δ薄膜。 X射线分析。最大功率密度在600摄氏度时达到1.05 W cm-(2),该值高于最近报道的质子传导陶瓷燃料电池(PCFC)的冠军数据。进行电化学阻抗分析以表征阳极和阴极的极化行为。用阴极电荷转移元件和阳极质量转移元件的串联连接建立的等效电路可以解释HMFC的阻抗响应。与正常燃料电池气氛中的阴极极化和欧姆损耗相比,Pd块中的传质贡献被发现相对较小。此外,发现HMFC的阴极电荷转移电阻比最近的PCFC系统小25倍。目前的结果表明,HMFC在BaCe0.8Y0.2O3-δ电解质和多孔La0.6Sr0.4Co0.2Fe0.8O3-δ阴极之间的界面附近保留了较大的气-质-电子三边界区。

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