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Enhancing photocatalytic activity of one-dimensional KNbO3 nanowires by Au nanoparticles under ultraviolet and visible-light

机译:提高光催化活性一维KNbO3 Au纳米线纳米粒子在紫外和可见光

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摘要

A novel photocatalyst was prepared by anchoring Au nanoparticles (NPs) onto one-dimensional potassium niobate (KNbO3) nanowires. Photocatalytic activity towards rhodamine B degradation over Au/KNbO3 appears to be much greater than that of KNbO3 nanowires, nanorods and commercial Alfa Aesar. in terms of reaction rate constant (k), ultraviolet excitation (X = 365 nm) is higher than that of visible-light (A > 420 nm) and increasing the size of Au NPs from 5 to 10 nm significantly improves the reactivity. Notably, Au NPs with a size of ca. 10 nm supported on KNbO3 nanowires display the greatest photoreactivity, with k exceeding that of commercial KNbO3 by a factor of 15. The mechanism responsible for the enhancement of photocatalytic activity was discussed, highlighting the crucial role of surface plasmon resonance as well as interband transitions on Au NPs. This study is potentially applicable to a range of low-dimensional niobate-based nanostructures combined with Au and other plasmonic NPs with promising applications in photocatalysis and relevant areas.
机译:一种新型光催化剂被锚定盟准备纳米颗粒(NPs)到一维铌酸钾纳米线(KNbO3)。对罗丹明B的光催化活性降解非盟/ KNbO3似乎太多了比KNbO3纳米线,纳米棒和商业阿尔法蛇丘。速率常数(k)、紫外线激发(X =365海里)高于可见光(>420海里)和增加的大小非盟NPs从510 nm显著提高了反应性。值得注意的是,非盟NPs与ca的大小。10纳米支持KNbO3纳米线显示最伟大photoreactivity, k的超过商业KNbO3 15倍。负责增强光催化活动进行了讨论,强调了重要表面等离子体共振的作用在非盟NPs带间的转换。可能适用于一系列的低维niobate-based纳米结构与非盟和其他电浆NPs相结合在光催化和有前途的应用程序相关的领域。

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