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Electrode surface modification for cathode catalysis in semi-fuel cells

机译:半燃料电池阴极催化电极表面改性

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The development of a catalyzed substrate toward the reduction of hydrogen peroxide in a semi-fuel cell is described. Long term reproducible performance and cell voltage over a broad range of current densities were studied. Characterization of theelectrocatalyst was performed using Scanning Electron Microscopy (SEM) and Energy Dispersive Spectrometer mapping. Electrodeposition was carried out by cyclic voltammetry. A combination of palladium and iridium outperformed palladium, iridium or silveralone as shown by electrode polarization curves and measured cell voltages at various current densities. The Pd/Ir combination was found to be more uniformly distributed on a high density planar carbon substrate than on a nickel substrate. The Pd/Ircombination exhibited clusters and film growth on the nickel substrate with large areas of the substrate uncovered. The carbon substrate was uniformly covered and showed only spherical clusters of fairly uniform size. Semi-fuel cell voltage measurementsover time and at various current densities showed the superior performance of the Pd/Ir combination on the high density carbon substrate without compromising the current density range of operation for the cell.
机译:描述了催化基材朝向半燃料电池中的过氧化氢的还原的研制。研究了长期可重复的性能和电池电压在广泛的电流密度上进行。使用扫描电子显微镜(SEM)和能量分散光谱仪映射进行电催化剂的表征。电沉积通过循环伏安法进行。钯和铱优于钯,铱或银酮的组合,如电极偏振曲线所示和各种电流密度的测量电池电压。发现PD / IR组合在高密度平面碳基底上比镍基材更均匀地分布。 Pd / Ircombination在镍基材上表现出簇和薄膜生长,其中覆盖大面积的基材。均匀地覆盖碳基材并仅显示相当均匀的球形簇。半燃料电池电压测量时间和各种电流密度显示PD / IR组合在高密度碳基板上的优异性能,而不会影响电池的电流密度的操作范围。

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