期刊文献+

掺杂Fe元素对Pd/C催化剂性能的影响 被引量:8

Effect of Adding Fe on the Performances of Pd/C Catalyst
下载PDF
导出
摘要 用Fe作为掺杂元素,以活性炭为载体,通过浸溃还原方法制备了Pd:Fe原子比分别为1:1、2:1、1:2的Pd-Fe/C催化剂.采用TEM和XRD技术对合金催化剂的物理性质进行了测试.结果表明,获得的Pd-Fe/C催化剂合金粒子在载体上分布均匀,粒径<5nm,Fe的掺杂量对Pd/C催化剂晶体结构有很大影响,通过电化学性能测试比较,分析了三个不同比例的Pd-Fe/C催化剂和Pd/C催化剂对氢和甲酸的电催化氧化性能.结果得出:在相同的峰值电位下,几种催化剂的电流密度大小顺序为:Pd-Fe/C(1:1)>Pd-Fe/C(2:1)>Pd/C>Pd-Fe/C(1:2).结果表明,适量掺杂Fe提高了Pd/C催化剂的催化性能。且Pd:Fe原子比为1:1时催化性能最好. Pd-Fe/C catalysts were prepared by the impregnation-reduction method. The ratios of Pd to Fe were 1:1, 2:1, 1:2, respectively. The catalysts were characterized by transmission electron microscope (TEM) and powder X-ray diffraction (XRD). The results indicate that the catalyst particles are homogeneously distributed in the carrier. The average particle sizes are less than 5nm. The influence of adding Fe on Pd/C catalyst crystal structure was also studied. Finally, the activation of Pd-Fe/C catalysts with different Pd/C ratios to the electrocatalytic oxidation of formic acid was investigated. The results show that the catalytic performances of Pd/C catalyst are improved by adding suitable Fe; the catalytic performance of the Pd-Fe/C catalysts reaches the best when the atom ration of Pd:Fe equal to 1:1.
出处 《无机材料学报》 SCIE EI CAS CSCD 北大核心 2008年第4期847-850,共4页 Journal of Inorganic Materials
基金 国家自然科学基金重点项目(20636060) 国家自然科学基金(50674006) 北京市自然科学基金重点项目(2051001)
关键词 直接甲酸燃料电池 Pd—Fe/C催化剂 电化学催化 direct formic acid fuel cell Pd-Fe/C catalyst electrochemical catalysis
  • 相关文献

参考文献19

  • 1陆天虹.直接醇类燃料电池——一种可能最早商品化的燃料电池[J].科学中国人,2005(1):51-51. 被引量:6
  • 2Zhu Y M, Ha S Y, Masel R I. J. Power Sources, 2004, 130 (1/2): 8-14.
  • 3Tamizhmani G, Gapuano G A. J. Electrochem. Soc., 1994, 14 (4): 968-970.
  • 4Shim J, Yoo D K, Lee J S.Electrochimica Acta, 2000, 45 (12): 1943-1951.
  • 5Xiong L, Kannan A M, Manthikam A, et al. Electrochem. Commun., 2002, 4 (11): 898-903.
  • 6Neergat M, Shukla A K, Gandhi K S.Journal of Applied Electrochemistry, 2001, 31 (4): 373-378.
  • 7李长志,文纲要,张颖,盖云天.PtCr/C-Nafion 膜氧电极的电催化活性[J].电源技术,1998,22(5):201-203. 被引量:10
  • 8Lee K, Savaziogo O, Ishihara A, et al. J. Electrochem. Soc., 2006, 153 (1): A20-A24.
  • 9Savadogo O, Lee K, Oishi K, et al. Electrochemistry Communications, 2004, 6 (2): 105-109.
  • 10Shao M H, Sasaki K, Adzic R R.Journal of American Chemical Society, 2006, 128 (7): 3526-3527.

二级参考文献17

  • 1苏爱华,李长志,孙公权,张颖,陆天虹.Pt/C-SPE和PtRu/C-SPE膜电极上甲醇的催化氧化[J].电化学,1995,1(4):397-401. 被引量:12
  • 2[3]Acres G J K. Recent advances in fuel cell technology and its applications[J]. Journal of Power Sources,2001, 100: 60- 66.
  • 3[4]Graham M, Barbir F, Marken F, et al. Fuel cell power system for utility vehicle[A]. In: Fuel Cell Seminar, Part 3 [C]. Oriando, Florida, USA, 1996. 40.
  • 4[5]Zhou D B, Vander Poorten H. Impedance characteristics of oxygen reduction at a platinum electrode in alkaline electrolyte[J]. J Electrochem Soc, 1998, 145(3):936 - 945.
  • 5[6]Min M K, Cho J, Cho K, et al. Particle size and alloying effects of Pt-based alloy catalysts for fuel cell applications[J]. Electrochimica Acta, 2000, 45: 4211-4217.
  • 6[7]Tamizhmani G, Gapuano G A. Improved electrocatalytic oxygen reduction performance of platinum ternary alloy-oxide in SPFCs[J]. J Electrochem Soc, 1994, 14(4): 968 - 970.
  • 7[8]Shim J, Yoo D K, Lee J S. Characteristics for electrocatalytic properties and hydrogen-oxygen adsorption of platinum ternary alloy catalysts in polymer electrolyte fuel cell[J]. Electrochimica Acta, 2000, 45: 1943 -1951.
  • 8[9]Xiong L, Kannan A M, Manthikam A, et al. Pt-M(M =Fe, Co, Ni and Cu) electrocatalysts synthesized by an aqueous route for proton exchange membrane fuel cells[J]. Electrochem Commun, 2002, 4(11): 898-903.
  • 9[10]Neergat M, Shukla A K, Gandhi K S. Platinumbased alloys as oxygen-reduction catalysts for solidpolymer-electrolyte direct methanol fuel cells [J].Journal of Applied Electrochemistry, 2001, 31 (4):373 - 378.
  • 10[13]Toda T, Hiroshi I, Masahiro W, et al. Enhancement of the electrocatalytic O2 reduction on Pt-Fe alloys[J]. J Electroanal Chem, 1999, 460(1 - 2): 258 -262.

共引文献34

同被引文献60

引证文献8

二级引证文献19

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