The influence of a new fabrication procedure on the catalytic activity of ruthenium-selenium catalysts

被引:39
作者
Cheng, H. [1 ]
Yuan, W. [1 ]
Scott, K. [1 ]
机构
[1] Newcastle Univ, Sch Chem Engn & Adv Mat, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
基金
英国工程与自然科学研究理事会;
关键词
electrocatalysis; direct methanol fuel cell; oxygen reduction reaction; ruthenium-selenium chalcogenides; methanol tolerant cathode materials;
D O I
10.1016/j.electacta.2006.05.028
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
A new procedure has been introduced to enhance catalytic activity of ruthenium-selenium electro-catalysts for oxygen reduction, in which materials are treated under hydrogen atmosphere at elevated temperatures. The characterisation using scanning electron microscopy, energy dispersive spectroscopy or energy dispersive X-ray spectroscopy exhibited that the treatment at 400 degrees C made catalysts denser while their porous nature remained, led to a good degree of crystallinity and an optimum Se:Ru ratio. The half cell test confirms feasibility of the new procedure; the catalyst treated at 400 degrees C gave the highest reduction current (55.9 mA cm(-2) at -0.4 V) and a low methanol oxidation effect coefficient (3.8%). The direct methanol fuel cell with the RuSe 400 degrees C cathode catalyst (2 mg RuSe cm(-2)) generated a power density of 33.8 mW cm(-2) using 2 M methanol and 2 bar oxygen at 90 degrees C. The new procedure produced the catalysts with low decay rates. The best sample was compared to the Pt and to the reported ruthenium-selenium catalyst. Possible reasons for the observations are discussed. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:466 / 473
页数:8
相关论文
共 20 条
  • [11] HUERTA RGG, 2005, J NEW MAT ELECTR SYS, V8, P15
  • [12] Nano-stuctured Pt-Fe/C as cathode catalyst in direct methanol fuel cell
    Li, WZ
    Zhou, WJ
    Li, HQ
    Zhou, ZH
    Zhou, B
    Sun, GQ
    Xin, Q
    [J]. ELECTROCHIMICA ACTA, 2004, 49 (07) : 1045 - 1055
  • [13] Oxygen reduction on high surface area Pt-based alloy catalysts in comparison to well defined smooth bulk alloy electrodes
    Paulus, UA
    Wokaun, A
    Scherer, GG
    Schmidt, TJ
    Stamenkovic, V
    Markovic, NM
    Ross, PN
    [J]. ELECTROCHIMICA ACTA, 2002, 47 (22-23) : 3787 - 3798
  • [14] Methanol-tolerant oxygen reduction catalysts based on transition metal sulfides and their application to the study of methanol permeation
    Reeve, RW
    Christensen, PA
    Dickinson, AJ
    Hamnett, A
    Scott, K
    [J]. ELECTROCHIMICA ACTA, 2000, 45 (25-26) : 4237 - 4250
  • [15] Recent advances in direct methanol fuel cells at Los Alamos National Laboratory
    Ren, XM
    Zelenay, P
    Thomas, S
    Davey, J
    Gottesfeld, S
    [J]. JOURNAL OF POWER SOURCES, 2000, 86 (1-2) : 111 - 116
  • [16] Oxygen reduction on Ru1.92Mo0.08SeO4, Ru/carbon, and Pt/carbon in pure and methanol-containing electrolytes
    Schmidt, TJ
    Paulus, UA
    Gasteiger, HA
    Alonso-Vante, N
    Behm, RJ
    [J]. JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2000, 147 (07) : 2620 - 2624
  • [17] Electrochemical selenium hydride generation with in situ trapping in graphite tube atomizers
    Síma, J
    Rychlovsky, P
    [J]. SPECTROCHIMICA ACTA PART B-ATOMIC SPECTROSCOPY, 2003, 58 (05) : 919 - 930
  • [18] Snyder R. L., 1999, X-ray characterization of materials, P1
  • [19] New catalysts for oxygen reduction based on transition-metal sulfides
    Trapp, V
    Christensen, P
    Hamnett, A
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1996, 92 (21): : 4311 - 4319
  • [20] ENERGY-CONVERSION CATALYSIS USING SEMICONDUCTING TRANSITION-METAL CLUSTER COMPOUNDS
    VANTE, NA
    TRIBUTSCH, H
    [J]. NATURE, 1986, 323 (6087) : 431 - 432