Citation: ZHAO Jing, SUN Yue, LI Yong-Jun, LIANG Ren. Preparation of ‘Sandwich-Like’ Au/Pt Composite Multilayer Films for Methanol Electrooxidation[J]. Acta Physico-Chimica Sinica, ;2011, 27(08): 1868-1874. doi: 10.3866/PKU.WHXB20110803 shu

Preparation of ‘Sandwich-Like’ Au/Pt Composite Multilayer Films for Methanol Electrooxidation

  • Received Date: 11 April 2011
    Available Online: 8 June 2011

    Fund Project: 国家自然科学基金(20703016) (20703016) 湖南省科技计划(2010FJ6030) (2010FJ6030)固体表面物理化学国家重点实验室(厦门大学)开放课题经费资助 (厦门大学)

  • Pt/Au composite monolayer films were fabricated by combining interfacial assembly and under-potential deposition (UPD) with redox replacement. Based on the Pt/Au composite monolayers, an organic linker-free method was proposed for the fabrication of sandwich-like Pt/Au composite multilayer films: (Pt/Au)n, Ptm/Au, and (Pt3/Au)k (n, m, or k represents the layer number). Electron microscopy was used to characterize the morphologies of the Au monolayer films and the Pt/Au composite multilayer films. For each type of composite multilayer films, a common characteristic was that the effective electroactive areas increased with an increase in the layer number. Additionally, the electrocatalytic activities of the composite multilayer films for methanol electrooxidation are systematically discussed by examining the catalytic current densities and its tolerance toward carbonaceous species. For the same series of composite multilayer films (Pt/Au)3, Pt3/Au, and (Pt3/Au)2 showed a higher catalytic current density than bulk Pt (Ptbulk). Among the three composite multilayer films, (Pt/Au)3 showed the best catalytic performance in terms of the current density and tolerance toward carbonaceous species. The tolerance of (Pt/Au)3 to carbonaceous species was found to be better than that of the commercial Pt/C catalyst. This better electrocatalytic activity may be attributed to the maximum synergistic effect between Au and Pt, which depends on the Pt:Au atomic ratio and also the arrangement of Pt and Au nanoparticles.

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