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TiO2纳米纺锤体负载Pt在氧还原反应中的应用

  • 彭桂明 ,
  • 巫素琴 ,
  • 彭全明 ,
  • BURKERT Seth C. ,
  • 杜瑞安 ,
  • 余长林 ,
  • STAR Alexander
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  • 1. 江西理工大学冶金与化学工程学院,江西 赣州 341000;
    2. 中国科学院可再生能源重点实验室,广州 510640;                        
    3. 广东工业大学材料与能源学院,广州 510006;
    4. 匹兹堡大学化学系,美国宾夕法尼亚州匹兹堡,15260

收稿日期: 2017-11-07

  修回日期: 2018-01-04

  网络出版日期: 2018-04-28

基金资助

中国科学院可再生能源重点实验室开放基金项目(Y707ka1001);
江西省自然科学基金项目(20171BAB213010);
江西省教育厅科学技术研究项目(GJJ160670)

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

摘要

燃料电池中催化剂的稳定性是影响其实际应用的关键问题之一。本研究合成了锐钛矿型纺锤状TiO2纳米材料,并负载纳米Pt制备了TiO2-Pt双组分复合催化材料。将其制作成电极材料后,进行了TEM、XRD、拉曼光谱、电化学特性分析。结果表明:TiO2-Pt材料中Pt纳米颗粒的TEM形貌与TiO2的表面亲和力有关;该双组分催化剂呈现出两个单独的氧还原反应(ORR)峰;在负载Pt后,材料电荷传输电阻明显减小,使得TiO2-Pt中TiO2纺锤体组分上的ORR性能明显增强;紫外光可同时促进TiO2-Pt中两组分的ORR性能;TiO2-Pt比炭黑负载Pt具有更好的稳定性。

本文引用格式

彭桂明 , 巫素琴 , 彭全明 , BURKERT Seth C. , 杜瑞安 , 余长林 , STAR Alexander . TiO2纳米纺锤体负载Pt在氧还原反应中的应用[J]. 新能源进展, 2018 , 6(2) : 163 -168 . DOI: 10.3969/j.issn.2095-560X.2018.02.011

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.

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