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Tungsten carbide/porous carbon core-shell nanocomposites as a catalyst support for methanol oxidation

机译:碳化钨/多孔碳核-壳纳米复合材料作为甲醇氧化的催化剂载体

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摘要

Carbon-encapsulated tungsten carbide (WC@C) was prepared by a microwave-assisted synthesis method with resorcinol-formaldehyde resin (RF) as carbon source. WC was encapsulated by porous carbon layer to form core-shell structure which could protect tungsten oxide from occupying the active sites on the surfaces of the WC@C. The characteristics of WC@C composites were determined by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, energy dispersive X-ray spectroscopy and Brunauer-Emmet-Teller gas adsorption. Platinum nanoparticles were uniformly distributed on WC@C to synthesize a new electrocatalyst Pt-WC@C. The electro-catalytic performances of prepared Pt-WC@C, commercial Pt/C and PtRu/C toward methanol oxidation were compared by cyclic voltammetry, chronoamperometry and CO stripping test. It was found that Pt-WC@C exhibited higher catalytic activity for methanol oxidation than that of commercial Pt/C and PtRu/C catalysts. Especially, the Pt-WC@C achieved the long-term stability which was attributed to the effective protection by the carbon porous shell structure.
机译:以间苯二酚-甲醛树脂(RF)为碳源,通过微波辅助合成法制备了碳包碳化钨(WC @ C)。 WC被多孔碳层包裹,形成核-壳结构,可以保护氧化钨不占据WC @ C表面的活性位。 WC @ C复合材料的特性通过X射线衍射,扫描电子显微镜,透射电子显微镜,能量色散X射线光谱和Brunauer-Emmet-Teller气体吸附来确定。铂纳米颗粒均匀地分布在WC @ C上以合成新的电催化剂Pt-WC @ C。通过循环伏安法,计时安培法和CO汽提试验,比较了制备的Pt-WC @ C,市售Pt / C和PtRu / C对甲醇氧化的电催化性能。结果发现,Pt-WC @ C对甲醇氧化的催化活性高于商用Pt / C和PtRu / C催化剂。尤其是,Pt-WC @ C获得了长期稳定性,这归因于碳多孔壳结构的有效保护。

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