Tuning the Photocatalytic Performance of Plasmonic Nanocomposites (ZnO/Aux) Driven in Visible Light

Aneeya K. Samantara, D. Dash, Diptimoyee Bhuyan, Namita Dalai, Bijayalaxmi Jena
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Abstract

In this article, we explored the possibility of controlling the reactivity of ZnO nanostructures by modifying its surface with gold nanoparticles (Au NPs). By varying the concentration of Au with different wt% (x = 0.01, 0.05, 0.08, 1 and 2), we have synthesized a series of (ZnO/Aux) nanocomposites (NCs). A thorough investigation of the photocatalytic performance of different wt% of Au NPs on ZnO nanosurface has been carried out. It was observed that ZnO/Au0.08 nanocomposite showed the highest photocatalytic activity among all concentrations of Au on the ZnO surface, which degrades the dye concentration within 2 minutes of visible light exposure. It was further revealed that with an increase in the size of plasmonic nanoparticles beyond 0.08%, the accessible surface area of the Au nanoparticle decreases. The photon absorption capacity of Au nanoparticle decreases beyond 0.08% resulting in a decrease in electron transfer rate from Au to ZnO and a decrease of photocatalytic activity. Due to the industrialization process, most of the toxic materials go into the water bodies, affecting the water and our ecological system. The conventional techniques to remove dyes are expensive and inefficient. Recently, heterogeneous semiconductor materials like TiO2 and ZnO have been regarded as potential candidates for the removal of dye from the water system. To investigate the photocatalytic performance of different wt% of Au NPs on ZnO nanosurface and the effect of the size of Au NPs for photocatalytic performance in the degradation process. A facile microwave method has been adopted for the synthesis of ZnO nanostructure followed by a reduction of gold salt in the presence of ZnO nanostructure to form the composite. ZnO/Au0.08 nanocomposite showed the highest photocatalytic activity which degrades the dye concentration within 2 minutes of visible light exposure. The schematic mechanism of electron transfer rate was discussed. Raspberry shaped ZnO nanoparticles modified with different percentages of Au NPs showed good photocatalytic behavior in the degradation of dye molecules. The synergetic effect of unique morphology of ZnO and well anchored Au nanostructures plays a crucial role.
等离子体纳米复合材料(ZnO/Aux)在可见光下的光催化性能
在本文中,我们探索了用金纳米粒子(Au NPs)修饰ZnO纳米结构的表面来控制其反应性的可能性。通过改变Au的wt% (x = 0.01, 0.05, 0.08, 1和2),我们合成了一系列(ZnO/Aux)纳米复合材料(NCs)。研究了不同wt% Au NPs在zno纳米表面上的光催化性能。结果表明,ZnO/Au0.08纳米复合材料在不同Au浓度的ZnO表面表现出最高的光催化活性,在可见光照射2分钟内降解染料浓度。进一步发现,当等离子体纳米粒子的尺寸增加到0.08%以上时,金纳米粒子的可达表面积减小。Au纳米粒子的光子吸收能力降低到0.08%以上,导致Au到ZnO的电子转移速率降低,光催化活性降低。由于工业化进程,大部分有毒物质进入水体,影响水体和生态系统。传统的去除染料的技术既昂贵又低效。近年来,非均相半导体材料如TiO2和ZnO被认为是去除水中染料的潜在候选材料。研究不同wt% Au NPs在ZnO纳米表面的光催化性能,以及Au NPs尺寸对降解过程光催化性能的影响。采用微波法合成ZnO纳米结构,并在ZnO纳米结构存在下还原金盐形成复合材料,ZnO/Au0.08纳米复合材料具有最高的光催化活性,在可见光照射2分钟内降解染料浓度。讨论了电子转移的示意图机制。不同比例Au nps修饰的覆盆子状ZnO纳米粒子在降解染料分子方面表现出良好的光催化性能。氧化锌的独特形貌和良好锚定的金纳米结构的协同效应起着至关重要的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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