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Pd-Au/C catalysts with different alloying degrees for ethanol oxidation in alkaline media

机译:不同合金化程度的Pd-Au / C催化剂在碱性介质中乙醇氧化

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摘要

High alloyed Pd-Au/C catalyst is prepared through a rate-limiting strategy in water/ethylene glycol solution. Pd/C and low alloyed Pd-Au/C catalysts are prepared with trisodium citrate and sodium borohydride as stabilizing and reducing agents, respectively. Transmission electron microscopy (TEM) shows that the synthesized Pd(Au) particles are well dispersed on the catalysts. X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) show that the high alloyed Pd-Au/C catalyst presents a relatively homogenous structure while the low alloyed Pd-Au/C catalyst presents a Pd-rich shell/Au-rich core structure. Electrochemical characterization shows that the low alloyed Pd-Au/C catalyst exhibits the best catalytic activity for ethanol oxidation reaction (EOR) in alkaline media, which could be attributed to its relatively large exposed Pd surface area as compared with the high alloyed Pd-Au/C catalyst due to its Pd-rich shell structure and its enhanced adsorption of OH_(ads) as compared with Pd/C catalyst due to its core-shell structure.
机译:通过限速策略在水/乙二醇溶液中制备高合金化的Pd-Au / C催化剂。 Pd / C和低合金化Pd-Au / C催化剂分别以柠檬酸三钠和硼氢化钠为稳定剂和还原剂制备。透射电子显微镜(TEM)显示合成的Pd(Au)颗粒很好地分散在催化剂上。 X射线衍射(XRD)和X射线光电子能谱(XPS)表明,高合金化Pd-Au / C催化剂呈现出相对均匀的结构,而低合金化Pd-Au / C催化剂呈现出富钯的壳/ Au丰富的核心结构。电化学表征表明,低合金化Pd-Au / C催化剂在碱性介质中对乙醇氧化反应(EOR)表现出最佳的催化活性,这可能是由于其与高合金化Pd-Au相比具有相对较大的暴露Pd表面积/ C催化剂是由于其富含Pd的壳结构,并且与Pd / C催化剂相比由于其核-壳结构而增强了对OH_(ads)的吸附。

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