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酸处理石墨化碳载体对燃料电池催化剂性能的影响 被引量:3

Effect of Acid-treatment of Graphitized Carbon Supports on Performance of Fuel Cell Catalysts
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摘要 通过1700℃高温处理XC-72CB得到石墨化碳黑(GCB),并采用酸处理对GCB碳载体进行官能团修饰.透射电子显微镜(TEM)、X射线粉末衍射(XRD)和拉曼光谱的结果显示,酸处理后GCB的石墨化程度增加;N2吸附-脱附结果证明GCB比表面积减小,微孔数量减少;热重分析结果表明,GCB热稳定性增强;红外光谱和拉曼光谱结果显示,GCB表面引入了含氧官能团,并同时保持了GCB的有序化结构.采用循环伏安(CV)法和线性扫描伏安(LSV)法测试了不同预处理后催化剂的电化学性能,表明其电化学活性表面积(ECSA,75.25 m^2/g)和质量比活性(MA,0.093 A/mg)均高于商业Pt/C(JM)催化剂.TEM结果表明,使用经过浓硫酸和浓硝酸混合酸处理的GCB(简称OGCB)作为载体得到的Pt/OGCB平均粒径为2.28 nm,略小于商业Pt/C(JM)催化剂(约2.5 nm);经5000周电化学循环伏安测试后,Pt/OGCB的电化学活性表面积衰减17.3%,质量比活性衰减29.5%,而Pt/C(JM)的ECSA衰减达到25.1%,MA衰减达到42.5%. The graphitized carbon black(GCB) was obtained by a high temperature(1700 ℃) treatment of the XC-72 commercial carbon black(XC-72 CB). The functional groups of GCB were modified by acid treatment. Transmission electron microscopy(TEM),X-ray diffraction,Raman spectrum and infrared spectroscopy displayed the GCB with acid treatment had a higher degree of graphitization. Oxygen- containing functional groups were introduced into the GCB surface and the ordered structure of the GCB was maintained at the same time. Nitrogen adsorption and desorption experiment showed the GCB had smaller specific surface area and less micropore compared to XC-72 CB. Thermogravimetric analysis showed that GCB had the better heat stability.Cyclic voltammetry and linear sweep voltammetry test showed that the electrochemical specific activity area(ECSA)(75.25 m2/g) and the mass activity(MA)(0.093 A/mg) of conc. H2SO4 and conc. HNO3 treated GCB(abbreviated as OGCB) were higher than those of the commercial one. TEM showed the Pt/OGCB had an average particle diameter of 2.28 nm,smaller than the commercial one. After durability test of 5000 cycles,the ECSA and MA of Pt/OGCB decreased by 17. 3% and 29. 5%,respectively,smaller than those of Pt/C(JM)(25.1% and 42.5%). Both activity and durability performance of Pt/OGCB catalyst were better than those of commercial Pt/C(JM) catalyst in oxygen reduction reaction. In addition,in single cell test,the durability of Pt/OGCB catalyst was also better than that of the commercial catalyst. The results show that OGCB has a promising application prospect in the field of proton exchange membrane fuel cell(PEMFC)catalyst support.
出处 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2016年第12期2236-2245,共10页 Chemical Journal of Chinese Universities
基金 国家自然科学基金(批准号:21276199) 中央高校基本科研基金(批准号:0500219216) 同济大学青年英才计划攀登高层项目及高等学校学科创新引智计划项目(批准号:B08019)资助~~
关键词 质子交换膜燃料电池 石墨化碳黑 酸处理 耐久性 Proton exchange membrane fuel cell Graphitized carbon black Acid treatment Durability
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  • 1张洁,唐水花,廖龙渝,郁卫飞.低温燃料电池非铂催化剂研究进展[J].催化学报,2013,34(6):1051-1065. 被引量:14
  • 2殷好勇,汪玲,聂秋林,徐铸德.Pt/TiO_2纳米管的制备及其电化学性能研究[J].杭州电子科技大学学报(自然科学版),2010,30(2):73-76. 被引量:1
  • 3王存国,何丽霞,董献国,王怡臻,赵树高,孙琳,林琳,肖红杰.用于锂离子电池的凝胶聚合物电解质的制备与性能[J].高等学校化学学报,2007,28(12):2373-2376. 被引量:10
  • 4麦克杜格尔.燃料电池[M]{H}北京:国防工业出版社,1983.
  • 5WANG Y J,DAVID P W,ZHANG J J. Noncarbon support materials for polymer electrolyte membrane fuel cell electrocatalysts[J].{H}Chemical Reviews,2011,(12):7625-7651.
  • 6MAASS S,FINSTERWALDER F,FRANK G. Carbon support oxidation in PEM Fuel cell cathodes[J].{H}Journal of Power Sources,2008.444-451.
  • 7SHEN Q,HOU M,LIANG D. Study on the processes of startup and shutdown in proton exchange membrane fuel cells[J].{H}Journal of Power Sources,2009,(02):1114-1119.
  • 8ROEN L M,PAIK C H,JARVIC T D. Electrocatalytic corrosion of carbon support in PEMFC cathodes[J].{H}Electrochemical and Solid-State Letters,2004,(01):A19.
  • 9HUANG S Y,POPOV P G,POPOV B N. Development of a titanium dioxide-supported platinum catalyst with ultrahigh stability for polymer electrolyte membrane fuel cell applications[J].{H}Journal of the American Chemical Society,2009.13898-13899.
  • 10HUANG S Y,GANESAN P,PARK S. Titania supported platinum catalyst with high electrocatalytic activity and stability for polymer electrolyte membrane fuel cell[J].{H}Applied Catalysis B:Environmental,2011.71-77.

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