期刊文献+

铂-氧化铈/聚苯胺/聚砜复合膜电极的制备及对甲醇的电催化氧化 被引量:1

Preparation of Pt-CeO_2/Polyaniline/Polysulfone Composite Film Electrode and Their Electrocatalytic Activity for Methanol Oxidation
下载PDF
导出
摘要 采用电化学聚合法制备了掺杂CeO2纳米粒子的聚苯胺(PAN)/聚砜(PSF)复合膜电极,在其上电沉积铂粒子,制得了铂-氧化铈/聚苯胺/聚砜的复合膜修饰电极。复合膜的形貌和化学组分通过冷场发射扫描电子显微镜(Cold FE-SEM)和能量散射X射线谱(EDS)进行了表征,用循环伏安法和电化学交流阻抗法考察了复合膜电极对甲醇的电催化氧化性能。结果表明,复合膜的双层多孔结构使铂粒子与CeO2粒子在复合膜内层的多孔聚苯胺上均匀沉积,粒子平均尺寸约为80 nm;CeO2为铂质量的7%时,铂-氧化铈/聚苯胺/聚砜复合膜修饰电极对甲醇有很好的电催化氧化性能和高的稳定性。 The polyaniline/polysulfone (PAN/PSF) composite film modified electrodes doped with cerium oxide were prepared by electropolymerization, and then Pt particles were deposited into this composite film to obtain the Pt modified cerium oxide/polyaniline/polysulfone (Pt-CeO2/PAN/PSF) electrodes. Their morphology and chemical component were characterized by field emission scanning electron microscopy (FESEM) and energy dispersive X-ray spectroscopy (EDS), respectively. Cyclic vohammetry (CV) and electrochemical impedance spectroscopy (EIS) techniques were applied to investigate the electrocatalytic activity of the electrode for methanol oxidation. The results show that the composite film has a hi-layer structure with asymmetrical pores, and platinum and cerium oxide particles are uniformly dispersed in the modified film electrodes. The average size of particles is about 80 nm. The electrode holds higher electro- catalytic activity and better stability for methanol oxidation on the condition of mass ratio between CeO2 and Pt is equal to 7%.
出处 《应用化学》 CAS CSCD 北大核心 2011年第3期302-307,共6页 Chinese Journal of Applied Chemistry
基金 河西学院西部资源环境化学重点实验室基金资助项目(XZ0706)
关键词 铂-氧化铈/聚苯胺/聚砜复合膜电极 电催化氧化 甲醇 Pt-CeO2/PAN/PSF composite film electrode, electrocatalytic oxidation, methnol
  • 相关文献

参考文献15

  • 1Cacciola G, Antonucci V, Freni S. Technology up Date and New Strategies on Fuel Cells [ J ]. J Power Sources,2001,100 (1/2) :67-79.
  • 2Liu Z L, Ling X Y, Su X,et al. Carbon-Supported Pt and PtRu Nanoparticles as Catalysts for a Direct Methanol Fuel Cell [ J]. J Phy Chem B,2004,108(24) :8234-8240.
  • 3Dubau L, Coutanceau C Gamier, et al. Electrooxidation of Methanol at Platinum-ruthenium Catalysts Prepared from Colloidal Precursors:Atomic Composition and Temperature Effects[J]. J Appl Electrochem,2003 ,33 :419-429.
  • 4Zhou W J,Zhou B,Li W Z,et al. Performance Comparison of Low-temperature Direct Alcohol Fuel Cells with Different Aanode Catalysts[ J]. J Power Sources ,2004,12.6 : 16-22.
  • 5Luo L Q, Futamata M. Competitive Adsorption of Water and CO on Pd Modified Pt Electrode from CH3 OH Solution[ J ]. Electrochem Commun ,2006,8:231-237.
  • 6Martinez A, Fernanez M, Conesa J C. Redox Interplay at Copper Oxide-( Ce, Zr) Ox Interfaces:Influence of the Presence of NO on the Catalytic Activity for CO Oxidation over CuO/CeZrO4 [ J ]. J Catal,2003,214:261-272.
  • 7Zimmer P, Tschope A, Birringer R. Temperature-programmed Eeaction Spectroscopy of Ceria- and Cu/ceria-supported Oxide Catalyst[ J ]. J Catal,2002,205 :339-345.
  • 8Liu Y Y, Hayakawa T, Suzuki K,et al. Highly Active Copper/ceria Catalysts for Steam Reforming of Methanol[ J ]. Appl Catal A ,2002,223( 1/2 ) : 137-145.
  • 9Kawaguchi T, Sugimoto W, Murakami Y. Temperature Dependence of the Oxidation of Carbon Monoxide on Carbon Supported Pt, Ru, and PtRu[ J]. Electrochem Commun,2004,6(5) :480-483.
  • 10Sugimoto W, Saida T, Takasu Y. Co-catalytic Effect of Nanostructured Ruthenium Oxide Towards Electro-oxidation of Methanol and Carbon Monoxide[ J]. Chem Commun ,2006,8(5 ) :411-415.

同被引文献9

引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部