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Chemically initiated liquid-like behavior and fabrication of periodic wavy Cu/CuAu nanocables with enhanced catalytic properties

机译:化学发起行为和液状物制造周期波浪铜/ CuAu nanocables具有增强的催化特性

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Solid crystalline materials have long range order in their atomic arrangement while liquids have short range order, and the transition between them is usually caused by heat and/or pressure. Herein, we report the finding that chemical processes may play a similar role as heat and initiate liquid-like behavior of crystalline nanomaterials at a temperature far below their melting points. When the straight Cu/CuAu crystalline nanocables are dispersed in organic amine at 8 degrees C under ambient conditions, the continuous oxidation of Cu atoms on the surface and diffusion of Cu atoms from the core to the surface would break up the long-range ordered arrangement of atoms and lead to the transformation of an anisotropic crystal into an isotropic liquid-like state, which resulted in the evolution of the straight morphology of the nanocables into periodic wavy structures following the Rayleigh instability. It was also demonstrated that periodic wavy Cu@CuAu nanocables exhibit much better catalytic activity than straight Cu@CuAu nanocables towards the reduction of p-nitrophenol into p-aminophenol by NaBH4. Our results not only provide new insights into the transition between a solid crystal and a liquid-like state at the nanoscale, but also facilitate the development of new strategies for the synthesis of functional nanomaterials.
机译:固体晶体材料具有长程有序在他们的原子排列而液体短程有序,之间的过渡他们通常是由热量和/或压力引起的。在此,我们报告的发现的化学物质过程可能发挥类似的作用和热启动水晶的液状物行为纳米材料在温度远低于他们熔点。水晶nanocables分散在有机食品胺在8摄氏度环境条件下,连续氧化的铜原子从核心表面和铜原子的扩散表面会分手远程有序排列的原子,导致的各向异性的晶体转变成一个各向同性的近似液态,这导致的直接形态的演变nanocables成周期性波浪结构瑞利后不稳定。表明周期性波浪Cu@CuAunanocables表现出更好的催化活性比直Cu@CuAu nanocables向减少p-nitrophenol到p-aminophenolNaBH4。为固体晶体和之间的过渡在纳米尺度上的近似液态,但也促进发展的新策略功能纳米材料的合成。

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