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首页> 外文期刊>Nanotechnology >Core-shell structured Co@CN nanocomposites as highly efficient dual function catalysts for reduction of toxic contaminants and hydrogen evolution reaction
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Core-shell structured Co@CN nanocomposites as highly efficient dual function catalysts for reduction of toxic contaminants and hydrogen evolution reaction

机译:核 - 壳结构CN纳米复合材料作为高效的双函数催化剂,用于减少有毒污染物和氢气进化反应

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In this study, we have reported nitrogen-doped graphite C coated Co nanocomposite (Co@CN) catalysts synthesized by one-step arc discharge method. The surface compositions, morphologies and the catalytic properties of the Co@CN nanocomposites were studied minutely. The results reveal that the prepared Co@CN nanocomposites have typical core-shell structure and show highly efficient catalytic performance in a reduction of 4-nitrophenol (4-NP), rhodamine and methylene blue. Their rate constant (K-app) is 0.074 s(?1) in a reduction of 4-NP, which is much higher than that of reported transition metal-based catalysts. Moreover, the overpotential of Co@CN is only 96 mV at a current density of 10 mA cm(?2) in alkaline solution, showing high electrocatalytic activities in the hydrogen evolution reaction. The excellent synergistic effect between nitrogen-doped graphite C shell and magnetic Co core enables the Co@CN nanocomposites catalysts to hold abundant active sites and to transmit rapidly electron ability, resulting in Co@CN nanocomposite catalysts having a highly efficient catalytic nature.
机译:在该研究中,我们已经报道了通过单步电弧放电方法合成的氮掺杂石墨C涂覆的CO纳米复合材料(CO @ CN)催化剂。 CO @ CN纳米复合材料的表面组合物,形态和催化性质进行了细微。结果表明,制备的CO纳米复合材料具有典型的核 - 壳结构,并在减少4-硝基苯酚(4-NP),罗丹明和亚甲基蓝色中表现出高效的催化性能。它们的速率常数(K-APP)为0.074秒(α1),减少4-NP,远高于报道的过渡金属基催化剂。此外,CO @ CN的过电位仅为碱性溶液中的10 mA cm(β2)的电流密度为96mV,在氢进化反应中显示出高电催化活性。氮掺杂石墨C壳和磁共核之间的优异协同效应使得CO @ CN纳米复合材料催化剂能够保持丰富的活性位点并传递快速的电子能力,得到具有高效催化性质的CO @ CN纳米复合催化剂。

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