期刊文献+

固相反应制备的Pt/C催化剂对乙醇氧化的电催化活性 被引量:11

Electrocatalytic Activity of Pt/C Catalyst Prepared with Solid Phase Reaction Method for Ethanol Oxidation
下载PDF
导出
摘要 用固相反应法制备了Pt/C催化剂(Pt/C(s)),并研究了该催化剂对乙醇氧化的电催化活性。XRD和TEM测量表明,Pt/C(s)中Pt的平均粒径为3.8nm,结晶度为2.38,远小于用传统的液相还原方法制得的Pt/C催化剂(Pt/C(1))的平均粒径(8.5nm)和结晶度(5.56)。因此,Pt/C(s)对乙醇的电催化氧化性能远好于液相还原法制得的Pt/C(1)。 The Pt/C catalyst (Pt/C(s)) was prepared with solid phase reaction method and its electrocatalytic activity for the ethanol oxidation was studied. XRD and TEM measurements indicated that the average diameter and the crystalline extent of Pt particles in Pt/C(s) are 3.8 nm and 2.38, respectively, which are much lower than the average diameter(8.5 nm) and the crystalline extent(5.56) of the Pt/C(l) catalyst prepared with the traditional liquid phase reaction method(Pt/C(l)). Therefore, the electrocatalytic activity of Pt/C(s) for the ethanol oxidation is much better than that of Pt/C(l). Cyclic voltammograms and chronoamperometric curves both confirmed this conclusion.
出处 《物理化学学报》 SCIE CAS CSCD 北大核心 2003年第11期1001-1004,共4页 Acta Physico-Chimica Sinica
基金 国家基础研究重大项目计划(G2000026408) 国家高技术研究计划(2001AA323060) 国家自然科学基金(20003005) 江苏省自然科学基金BQ2000009) 江苏省教育厅高新技术产业化基金(JH02-080) 吉林省自然科学基金(20000510) 国家"211"工程重点学科建设资助项目~~
关键词 固相反应 制备 PT/C 催化剂 乙醇 氧化 电催化活性 燃料电池 solid phase reaction ethanol fuel cell Pt/C catalyst
  • 相关文献

参考文献8

  • 1[1]Hogarth, M. P.; Hards, G. A. Platinum Metals Rev., 1996,40:150
  • 2[2]Witham, C. K.; Chun, W.; Valdez, T. I.; Narayanan, S. R.Electrochem. and Solid-State Letters, 2000, 3:497
  • 3[3]Watanabe, M.; Uchida, M.; Motoo, S. J. Electroanal.Chem., 1987, 229:395
  • 4[5]Schmidt, T. J.; Noeske, M.; Gasteiger, H. A. Langmuir,1997, 13:2591
  • 5[6]White, J. H.; Sammells, A. F. J. Electrochem. Soc., 1993,140:2167
  • 6[7]Antolini, E.; Cardelini, F. J. Alloys and Compounds, 2001,315:118
  • 7[8]Lamy, C.; Lima, A.; Lerhun, V.; Delime, F.; Coutanceau,C.; Leger, J.M. J. Power Sources, 2002, 105:283
  • 8[9]Snell, K. D.; Keenan, A. G. Electrochim. Acta, 1981, 26:1399

同被引文献92

引证文献11

二级引证文献52

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