4.7 Article

Novel synthesis of core-shell Au-Pt dendritic nanoparticles supported on carbon black for enhanced methanol electro-oxidation

期刊

APPLIED SURFACE SCIENCE
卷 433, 期 -, 页码 840-846

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.apsusc.2017.10.104

关键词

Core-shell structure; Au-Pt; Electrocatalysis; Methanol oxidation

资金

  1. National Natural Science Foundation of China [51572073]
  2. Wuhan Youth Science and Technology Morning Program [2014072704011252]
  3. Natural Science Foundation of Hubei Province [2015CFA119]
  4. Key Laboratory of Tobacco Chemistry Foundation of Yunnan Province [2016539200340109]

向作者/读者索取更多资源

Core-shell Au-Pt dendritic nanoparticles (Au-Pt NPs) has been synthesized via a facile seed-mediated growth method, in which dendritic Pt nanoparticles as shell grow on the surface of gold nanocores by using ascorbic acid (AA) as green reducing reagents. The morphologies and compositions of the as-prepared nanocomposites with core-shell structure are characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS). Electrochemical experiments, including cyclic voltammetry (CV) and chronoamperometry (CA) are performed to investigate the electrocatalytic properties of the Au-Pt NPs loaded carbon black composites (Au-Pt NPs/V) towards methanol oxidation in an alkaline solution. It is found that the reduction time of AA could regulate the thickness and amount of Pt on the Au nanocores, which significantly affect catalytic activity of the Au-Pt NPs/V toward methanol oxidation. Au-Pt NPs/V with optimum reduction time 4 h exhibit 2.3-times higher electrocatalytic activity than that of a commercial catalyst (Pt/carbon black) and an excellent CO tolerance toward methanol oxidation. This behavior is attributed to large active electro-chemical area of the bimetallic nanocomposites and the change in the electronic structure of Pt when Au surface modified with fewer Pt nanoparticles. (C) 2017 Elsevier B.V. All rights reserved.

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