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首页> 外文期刊>Journal of nanoscience and nanotechnology >Catalysis of Methanol Oxidation on Bimetallic Ir/Pt(poly) Electrodes
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Catalysis of Methanol Oxidation on Bimetallic Ir/Pt(poly) Electrodes

机译:双金属IR / PT(多)电极对甲醇氧化的催化

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摘要

Oxidation of methanol was studied in alkaline solution on bimetallic Ir/Pt(poly) catalysts prepared by the spontaneous deposition of Ir on polycrystalline Pt. Nano-scale surface properties of Ir/Pt(poly) catalysts were revealed by ex situ Atomic Force Microscopy imaging. Modified electrodes were characterized in situ electrochemically by cyclic voltammetry in 0.1 M KOH. Investigations of the methanol oxidation in the same alkaline solution showed that Ir/Pt(poly) electrode obtained after 1 minute Ir deposition, which is equivalent to 80% Ir coverage, showed improved activity with respect to both constitutive metals. The observed synergism on the methanol oxidation activity was ascribed to both bifunctional and electronic effects that are induced by the presence of spontaneously deposited Ir. The origin of the synergism and the possible methanol oxidation pathways were discussed on the basis of the activities of the Ir/Pt(poly) electrodes for the oxidation of the most probable reaction intermediates, CO and formaldehyde, in the same alkaline solution.
机译:通过在多晶体Pt上自发沉积的二氧化硅IR / Pt(多种)催化剂上的双金属溶液对碱性溶液进行氧化氧化。通过Ex原位原子力显微镜显微镜揭示IR / Pt(多)催化剂的纳米级表面性质。通过在0.1M KOH中通过循环伏安法在原位的改性电极表征。相同碱性溶液中甲醇氧化的研究表明,1分钟IR沉积后获得的IR / Pt(多)电极,其相当于80%IR覆盖,显示出相对于两个本构金属的活性。观察到对甲醇氧化活性的协同作用归因于通过自发沉积的IR的存在诱导的双官能和电子效应。基于IR / Pt(多种)电极的活性,用于氧化最可能反应中间体,CO和甲醛,在相同的碱性溶液中的氧化的活性和可能的​​甲醇氧化途径的起源。

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