首页> 外文期刊>Chemistry of Materials: A Publication of the American Chemistry Society >Synthesis of Bimetallic Au@Pt Nanoparticles with Au Core and Nanostructured Pt Shell toward Highly Active Electrocatalysts
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Synthesis of Bimetallic Au@Pt Nanoparticles with Au Core and Nanostructured Pt Shell toward Highly Active Electrocatalysts

机译:具有金核和纳米结构的Pt壳的双金属Au @ Pt纳米粒子对高活性电催化剂的合成

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摘要

Au@Pt nanocolloids with nanostructured dendritic Pt shells are successfully synthesized by chemically reducing both H2PtCl6 and HAuCl4 species in the presence of a low-concentration surfactant solution. By applying an ultrasonic treatment, the particle size of the Au@Pt nanocolloids is dramatically decreased and their size distribution becomes very narrow. The difference in reduction potentials of the two soluble metal salts (Au(III) and Pt(IV) species) plays a key role in the one-step synthesis of the core-shell structure. Because of the different reduction potentials, the reduction of Au ions preferentially occurs over a short time to form the Au seeds. It is followed by overgrowth of Pt nanodendritic nanowires on the Au seeds, which is confirmed by ultraviolet—visible light absorption spectroscopy and transmission electron microscopy. Interestingly, the Pt shell thicknesses on Au cores can be easily tuned by controlling the Pt/Au molar ratios in the starting precursor solutions. Through the optimization of the Pt shell thicknesses, the Au@Pt nanocolloids can exhibit enhanced activity as an electrocatalyst for a methanol oxidation reaction, which will be important to improve the utilization efficiency of Pt catalysts in the future.
机译:通过在低浓度表面活性剂溶液中化学还原H2PtCl6和HAuCl4物种,成功合成了具有纳米结构树突状Pt壳的Au @ Pt纳米胶体。通过应用超声波处理,Au @ Pt纳米胶体的粒径显着减小,并且其粒径分布变得非常狭窄。两种可溶性金属盐(Au(III)和Pt(IV)物种)还原电位的差异在核-壳结构的一步合成中起关键作用。由于不同的还原电位,Au离子的还原优先在短时间内发生,以形成Au晶种。随后,Au种子上的Pt纳米树枝状纳米线过度生长,这已通过紫外可见光吸收光谱法和透射电子显微镜得到证实。有趣的是,通过控制起始前体溶液中的Pt / Au摩尔比,可以轻松调整Au核上的Pt壳厚度。通过优化Pt壳的厚度,Au @ Pt纳米胶体可以作为甲醇氧化反应的电催化剂表现出增强的活性,这对于将来提高Pt催化剂的利用率非常重要。

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