Chemical Reduction and Deposition of Nanostructured Pt–Au Alloy

ular method (Herricks, Chen & Xia, 2004; Ouyang & Cho, 2011; Skrabalak, Wiley, Kim, Formo, & Xia, 2008). The chemical reduction method uses a reducing agent, such as NaBH4 and LiBEt3H, to reduce metal precursors to their pure metallic form (Gonsalvesa, Rangarajan & Wang, 2000). By controlling the experimental conditions, like the pH and precursor concentration, the shape, size and composition of NMA are well-controlled, making this method the most popular (Ouyang & Cho, 2011). Most studies employ complex chemical reduction methods to produce NMA with high catalytic capabilities. They include heating at high temperatures over 300°C (Ganesan, Freemantle, & Obare, 2007; Jana, Dutta, Bera, & Koner, 2008) or using complicated postnanoparticle immobilisation processes like layer-bylayer deposition (Ouyang & Cho, 2011). A convenient chemical reduction method by Ouyang & Cho (2011) is the low heat, solvent-free polyol reduction. The reducing agent used is ethylene glycol (EG), which is vaporized under low heat (below 200°C) so that the vapour will reduce metal precursors. EG is then oxidized to aldehydes and carboxylic acids. Gaseous products from this reaction will escape into the air, leaving the NMA end-product free of any liquid organic compounds. The formed NMA will have well-defined shapes and good adhesion to glass substrates. Thus, no additional steps of mixing metal precursors with surfactants and additives, which control the shapes, are required. Here we investigate the deposition of Pt–Au NMA of varying Pt:Au mass loading ratios on fluorine-doped tin oxide (FTO) glass substrates using the low heat, solvent-free polyol reduction by Ouyang & Cho (2011). We evaluate the hypothesis that the low heat, solvent-free polyol reduction method is able to produce the Pt–Au NMA that has better catalytic ability than that of pure Pt. We also investigate the role that the Pt:Au ratio plays in determining the catalytic capability of Pt–Au NMA. INTRODUCTION Platinum (Pt) nanoparticles act as catalysts in proton exchange membrane (PEM) fuel cells powering machinery (Bing, Liu, Zhang, Ghosh, & Zhang, 2010; Ouyang & Cho, 2011). Using H2 or liquid fuels like CH3OH, PEM fuel cells, made up of acid-soaked PEM placed in between the anode and cathode catalyst, oxidize the fuel at the cathode and reduce the oxygen entering the cell. This creates a potential difference, V, that drives an electric current. Said electric current can be used to power a variety of applications. The fuel cell could use a Pt plate or Pt coated substrate as either the anode or cathode catalysts. It has been reported in studies that by combining Pt with other metals to form nanostructured metal alloys (NMA), the adsorption of carbonaceous poisoning species like CO is suppressed (Ren et al., 2010). Such poisoning species tend to permanently bind themselves to the catalyst, leaving less sites for the oxidation and reduction of chemical species responsible for driving the electric current. Less adsorption of poisoning species in NMA catalysts can lead to enhanced catalytic performance. NMA can be chemically deposited on substrates in the same way as pure metal nanoparticles do. There are several deposition methods, of which the chemical reduction method is the most popChemical Reduction and Deposition of Nanostructured Pt–Au Alloy