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Influence of CeO2 on Pt-Pd/CeO2-OMC Catalysts for Formic Acid Oxidation

机译:CeO2对Pt-Pd / CeO2-OMC甲酸氧化催化剂的影响

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This article deals with the promotional effects of CeO2 on PtPd/CeO2-OMC electrocatalysts. The synthesized catalysts are characterized using different physicochemical techniques and evaluated in a formic acid oxidation fuel cell. N-2 adsorption/desorption analysis shows that CeO2 modification increases the surface area of OMC from 1005 to 1119 m(2)/ g. SEM, XRD, and TEM analysis reveal that the presence of CeO2 enhances the active metal(s) dispersion on the CeO2-OMC surface. The average particle size of the dispersed metal decreases with the increase of Pt/Pd ratio on CeO2-OMC support. Cyclic voltametry measurement of Pd/CeO2-OMC gives 12% higher anodic current activity with 83-mV negative shift of the peak E as compared to unmodified Pd/OMC. In bimetallic catalysts, the addition of Pt improves the activity and stability of the catalysts significantly. Among the bimetallic samples, Pd3Pt1/CeO2-OMC displays superior current density (74.6 mA/cm(2)), which is 28.3 times higher than that of Pt/CeO2-OMC. It also shows higher stability (on 32.8 mA/cm(2)) for an extended period of time (30 min) with least indication of CO poisoning effects.
机译:本文讨论了CeO2对PtPd / CeO2-OMC电催化剂的促进作用。使用不同的物理化学技术对合成的催化剂进行表征,并在甲酸氧化燃料电池中进行评估。 N-2吸附/解吸分析表明CeO2改性使OMC的表面积从1005增加到1119 m(2)/ g。 SEM,XRD和TEM分析表明CeO2的存在增强了CeO2-OMC表面活性金属的分散性。随着CeO2-OMC载体上Pt / Pd比的增加,分散金属的平均粒径减小。与未经修饰的Pd / OMC相比,Pd / CeO2-OMC的循环伏安法测量可提供12%的阳极电流活性,且峰E的负位移为83-mV。在双金属催化剂中,Pt的添加显着提高了催化剂的活性和稳定性。在双金属样品中,Pd3Pt1 / CeO2-OMC显示出优越的电流密度(74.6 mA / cm(2)),比Pt / CeO2-OMC高28.3倍。它还在较长的时间段(30分钟)内显示出更高的稳定性(在32.8 mA / cm(2)上),并且几乎没有显示CO中毒的迹象。

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