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Ethanol electrooxidation on PdIr/C electrocatalysts in alkaline media: electrochemical and fuel cell studies

机译:碱性介质中PdIr / C电催化剂上的乙醇电氧化:电化学和燃料电池研究

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摘要

PdIr/C electrocatalysts in different atomic ratios (Pd:Ir 90:10, 70:30, and 50:50), Pd/C and Ir/C supported on Vulcan XC 72 carbon were tested for ethanol electrooxidation in alkaline media. The electrocatalysts were prepared by borohydride reduction method. The electrocatalysts were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), energy dispersive spectroscopy (EDS), cyclic voltammetry (CV), and chronoamperometry (CA). The XRD measurements suggested the PdIr alloy formation. EDS analyses showed the real atomic ratios similar to the nominal ones. TEM showed the average particle diameter between 4.6 and 5.8 nm for all compositions prepared. The catalytic activity for ethanol electrooxidation in alkaline medium investigated by CV and CA at room temperature showed that PdIr/C (90:10) exhibited higher performance for ethanol oxidation in comparison with others PdIr/C compositions, Pd/C and Ir/C, while the experiments on a single direct ethanol alkaline fuel cell at 70 A degrees C showed higher performance for PtIr (70:30). The best results obtained using PdIr/C electrocatalysts may be associated to the electronic effect between Pd and Ir that might cause a decrease of poisoning on catalyst and the occurrence of bifunctional mechanism.
机译:测试了不同原子比(Pd:Ir 90:10、70:30和50:50),负载在Vulcan XC 72碳上的Pd / C和Ir / C的PdIr / C电催化剂在碱性介质中的乙醇电氧化作用。用硼氢化物还原法制备了电催化剂。通过X射线衍射(XRD),透射电子显微镜(TEM),能量色散谱(EDS),循环伏安法(CV)和计时电流法(CA)对电催化剂进行表征。 XRD测量表明存在PdIr合金。 EDS分析显示实际原子比与标称原子比相似。 TEM显示所制备的所有组合物的平均粒径在4.6至5.8nm之间。 CV和CA在室温下对碱性介质中乙醇电氧化的催化活性表明,与其他PdIr / C组合物Pd / C和Ir / C相比,PdIr / C(90:10)表现出更高的乙醇氧化性能。而在70 A摄氏度的单个直接乙醇碱性燃料电池上进行的实验显示了更高的PtIr性能(70:30)。使用PdIr / C电催化剂获得的最佳结果可能与Pd和Ir之间的电子效应有关,这可能导致催化剂中毒的减少和双功能机理的发生。

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