The influence of membrane electrode assembly water content on the performance of a polymer electrolyte membrane fuel cell as investigated by 1H NMR microscopy

被引:33
作者
Feindel, Kirk W. [1 ]
Bergens, Steven H. [1 ]
Wasylishen, Roderick E. [1 ]
机构
[1] Univ Alberta, Dept Chem, Gunning Lemieux Chem Ctr, Edmonton, AB T6G 2G2, Canada
关键词
D O I
10.1039/b617551a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The relation between the performance of a self-humidifying H-2/O-2 polymer electrolyte membrane fuel cell and the amount and distribution of water as observed using H-1 NMR microscopy was investigated. The integrated H-1 NMR image signal intensity (proportional to water content) from the region of the polymer electrolyte membrane between the catalyst layers was found to correlate well with the power output of the fuel cell. Several examples are provided which demonstrate the sensitivity of the H-1 NMR image intensity to the operating conditions of the fuel cell. Changes in the O-2(g) flow rate cause predictable trends in both the power density and the image intensity. Higher power densities, achieved by decreasing the resistance of the external circuit, were found to increase the water in the PEM. An observed plateau of both the power density and the integrated H-1 NMR image signal intensity from the membrane electrode assembly and subsequent decline of the power density is postulated to result from the accumulation of H2O(l) in the gas diffusion layer and cathode flow field. The potential of using H-1 NMR microscopy to obtain the absolute water content of the polymer electrolyte membrane is discussed and several recommendations for future research are provided.
引用
收藏
页码:1850 / 1857
页数:8
相关论文
共 88 条
  • [1] Appleby AJ, 1999, SCI AM, V281, P74, DOI 10.1038/scientificamerican0799-74
  • [2] Gas evolution and power performance in direct methanol fuel cells
    P. Argyropoulos
    K. Scott
    W.M. Taama
    [J]. Journal of Applied Electrochemistry, 1999, 29 (6) : 663 - 671
  • [3] Carbon dioxide evolution patterns in direct methanol fuel cells
    Argyropoulos, P
    Scott, K
    Taama, WM
    [J]. ELECTROCHIMICA ACTA, 1999, 44 (20) : 3575 - 3584
  • [4] Barbir F, 2005, SUSTAIN WORLD SER, P1
  • [5] Neutron imaging technique for in situ measurement of water transport gradients within Nafion in polymer electrolyte fuel cells
    Bellows, RJ
    Lin, MY
    Arif, M
    Thompson, AK
    Jacobson, D
    [J]. JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1999, 146 (03) : 1099 - 1103
  • [6] Water management in PEM fuel cells
    Berg, P
    Promislow, K
    St Pierre, J
    Stumper, J
    Wetton, B
    [J]. JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2004, 151 (03) : A341 - A353
  • [7] Review of proton exchange membrane fuel cell models
    Biyikoglu, A
    [J]. INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2005, 30 (11) : 1181 - 1212
  • [8] Brown LF, 2001, INT J HYDROGEN ENERG, V26, P381, DOI 10.1016/S0360-3199(00)00092-6
  • [9] Callaghan P.T., 1991, Principles of nuclear magnetic resonance microscopy, V1st
  • [10] A nonelectrochemical reductive deposition of ruthenium adatoms onto nanoparticle platinum: anode catalysts for a series of direct methanol fuel cells
    Cao, DX
    Bergens, SH
    [J]. ELECTROCHIMICA ACTA, 2003, 48 (27) : 4021 - 4031