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A facile one-pot oxidation-assisted dealloying protocol to massively synthesize monolithic core-shell architectured nanoporous copper@cuprous oxide nanonetworks for photodegradation of methyl orange

机译:一种简便的一锅氧化辅助脱合金协议,可大规模合成单核芯壳结构的纳米多孔铜@氧化亚铜纳米网络,用于甲基橙的光降解

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摘要

In this report, a facile and effective one-pot oxidation-assisted dealloying protocol has been developed to massively synthesize monolithic core-shell architectured nanoporous copper@cuprous oxide nanonetworks (C-S NPC@Cu2O NNs) by chemical dealloying of melt-spun Al 37 at.% Cu alloy in an oxygen-rich alkaline solution at room temperature, which possesses superior photocatalytic activity towards photodegradation of methyl orange (MO). The experimental results show that the as-prepared nanocomposite exhibits an open, bicontinuous interpenetrating ligament-pore structure with length scales of 20 ± 5 nm, in which the ligaments comprising Cu and Cu2O are typical of core-shell architecture with uniform shell thickness of ca. 3.5 nm. The photodegradation experiments of C-S NPC@Cu2O NNs show their superior photocatalytic activities for the MO degradation under visible light irradiation with degradation rate as high as 6.67 mg min-1 gcat -1, which is a diffusion-controlled kinetic process in essence in light of the good linear correlation between photodegradation ratio and square root of irradiation time. The excellent photocatalytic activity can be ascribed to the synergistic effects between unique core-shell architecture and 3D nanoporous network with high specific surface area and fast mass transfer channel, indicating that the C-S NPC@Cu2O NNs will be a promising candidate for photocatalysts of MO degradation.
机译:在本报告中,已经开发了一种简便有效的一锅式氧化辅助脱合金方案,以通过熔融纺丝Al 37的化学脱合金来大规模合成整体式核壳结构纳米孔铜@氧化亚铜纳米网络(CS NPC @ Cu2O NNs)。在室温下在富氧碱性溶液中的0.1%Cu合金具有优异的对甲基橙(MO)光降解的光催化活性。实验结果表明,所制备的纳米复合材料呈现出开放的,双连续的互穿的韧带孔结构,其长度尺度为20±5 nm,其中包含Cu和Cu2O的韧带是典型的核壳结构,壳厚均一。 。 3.5纳米CS NPC @ Cu2O NNs的光降解实验表明,它们在可见光照射下对MO的降解具有优异的光催化活性,降解速率高达6.67 mg min-1 gcat -1,从本质上讲是一个扩散控制的动力学过程。光降解率与照射时间的平方根之间具有良好的线性关系。优异的光催化活性可归因于独特的核-壳结构与具有高比表面积和快速传质通道的3D纳米多孔网络之间的协同效应,这表明CS NPC @ Cu2O NNs将成为MO降解光催化剂的有希望的候选者。

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