IEEE Electron Device

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2010:19.2.1–19.2.4. Competing interests The authors declare that they have no competing interests. Authors’ contributions AP and DJ reviewed the papers under the instruction of SM. AP wrote the first draft and DJ prepared Tables 1 and 2 carefully under the instruction of SM. The final draft was modified by SM. All authors read and approved the final manuscript.”
“Background Catalysts using metal nanoparticles have been one of the most interesting research areas in recent years since its relevance to chemical [1–4], pharmaceutical [5–8], and energy-related applications [9–11]. Recently, some buy Pictilisib researchers have shown that nanocatalysts with high dispersion and narrow size distributions stabilized by appropriate supports or capping materials can work under mild conditions with high activity and high selectivity when compared to conventional heterogeneous catalysts. It is known that the transition metal nanoparticles are effective catalysts, in which the shape, size, and surface structure of the solid supports all that contribute to the

catalytic activity [1–4, 9–13]. The supports usually are alumina, zeolite, Non-specific serine/threonine protein kinase and carbon materials that further include the carbon black, carbon nanotubes, graphene, and nanoporous carbon [14–20]. Graphene is the most important and eye-catching carbon material since 2004 [21]. The graphene as catalyst support is known with many applications, such as in catalysis, in photodevices, and in enhancing electronic property [22–24]. Conventionally, the synthesis of metal nanoparticles on graphene follows the methods of polyol reduction, hydrothermal and solvothermal synthesis, and CVD, etc. [21–24]. In this study, we employed a simple method to synthesize the nanocomposite, abbreviated as Pt/GE and Pt/GO, in that the Pt precursor was dissolved in just the ionic liquid of 2-hydroxyethanaminium formate [HOCH2CH2NH3][HCO2], without any additional organic solvents or any additional reducing agents in the system. And this method was further microwave-assisted so that the synthesis was more efficient in time and less wasting in energy. The total synthesis was accomplished under 20 min.