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Synthesis of TiO2 Nanospindles Supported Pt Nanodots for Oxygen Reduction Reaction

  • PENG Gui-ming ,
  • WU Su-qin ,
  • PENG Quan-ming ,
  • BURKERT Seth C. ,
  • DU Rui-an ,
  • YU Chang-lin ,
  • STAR Alexander
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  • 1. School of Metallurgy and Chemical Engineering, Jiangxi University of Science and Technology,  Ganzhou 341000, Jiangxi, China;                
    2. CAS Key Laboratory of Renewable Energy, Guangzhou 510640, China;
    3. School of Materials and Energy, Guangdong University of Technology, Guangzhou 510006, China;
    4. Department of Chemistry, University of Pittsburgh, Pittsburgh, Pennsylvania, 15260, United States

Received date: 2017-11-07

  Revised date: 2018-01-04

  Online published: 2018-04-28

Abstract

The long-term stability of the catalysts for fuel cell reactions is one of the obstacles that limit their practical application. Herein, anatase TiO2 nanospindles were synthesized as a support for the growth of Pt nanodots to obtain a TiO2-Pt catalyst for oxygen reduction reaction (ORR). TEM, XRD, Raman spectrum, and electrochemical testing were employed to characterize the properties of TiO2-Pt catalyst. Results showed as following: the morphology of Pt nanodots on TiO2-Pt catalyst was dependent on the surface affinity of TiO2 nanospindles; there were two individual ORR peaks of the dual-component catalyst; after Pt deposition, the ORR performance of the catalyst was enhanced, which was ascribed to the accelerated surface charge transport through the Pt nanodots; the oxygen reduction performance on both components of  TiO2-Pt catalyst were promoted by ultraviolet light illumination; the long-term stability of TiO2-Pt nanospindle was better than that of commercial carbon black supported Pt catalyst.

Cite this article

PENG Gui-ming , WU Su-qin , PENG Quan-ming , BURKERT Seth C. , DU Rui-an , YU Chang-lin , STAR Alexander . Synthesis of TiO2 Nanospindles Supported Pt Nanodots for Oxygen Reduction Reaction[J]. Advances in New and Renewable Energy, 2018 , 6(2) : 163 -168 . DOI: 10.3969/j.issn.2095-560X.2018.02.011

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