School of Materials Science and Engineering, The University of New South Wales, Sydney, NSW 2052, Australia.
Langmuir. 2013 Jun 11;29(23):7134-42. doi: 10.1021/la400753q. Epub 2013 May 31.
Silver-gold (Ag-Au) bimetallic nanowires were controllably synthesized by a newly developed wet-chemical method at room temperature. The Ag nanowires and Au nanoparticles were sequentially formed by reduction with vanadium oxide (V2O3) nanoparticles so as to form Ag-Au bimetal, in which the Ag nanowires show a diameter of ~20 nm and length up to 10 μm. A few unique features were noted in our new approach: it was rapid (within a few minutes), controllable in shape and size, reproducible, and there was no need for any surface modifiers. The formation and growth mechanisms of these Ag-Au bimetallic nanostructures driven by lattice match and a unique reducing agent (V2O3) have been proposed in this study. Moreover, the application of such bimetallic nanoparticles for catalytic reduction of 4-nitrophenol to 4-aminophenol was performed, and they exhibit catalytic properties superior to those of the Ag nanowires, Au nanoparticles, and Ag-Pd bimetallic nanostructures prepared under the reported conditions. These Ag-Au bimetallic nanoparticles have potential to be highly efficient catalysts for the reduction of 4-nitrophenol. This study may lead to new path for the generation of other bimetallic nanostructures with excellent catalytic efficiency.
银金(Ag-Au)双金属纳米线在室温下通过新开发的湿化学方法可控合成。Ag 纳米线和 Au 纳米颗粒通过氧化钒(V2O3)纳米颗粒的还原依次形成,从而形成 Ag-Au 双金属,其中 Ag 纳米线的直径约为 20nm,长度可达 10μm。在我们的新方法中注意到了一些独特的特征:它快速(在几分钟内),形状和尺寸可控,可重复,并且不需要任何表面改性剂。本研究提出了晶格匹配和独特还原剂(V2O3)驱动下这些 Ag-Au 双金属纳米结构的形成和生长机制。此外,还对这种双金属纳米颗粒用于催化还原 4-硝基苯酚为 4-氨基酚的应用进行了研究,它们表现出的催化性能优于在报道条件下制备的 Ag 纳米线、Au 纳米颗粒和 Ag-Pd 双金属纳米结构。这些 Ag-Au 双金属纳米颗粒有望成为高效的 4-硝基苯酚还原催化剂。本研究可能为生成具有优异催化效率的其他双金属纳米结构开辟新途径。