Voltage-concentration relations with enhanced slopes in electrochemical cells based on Nafion®

被引:17
作者
Jak, MJG
Raz, S
van Rij, LN
Schoonman, J
Riess, I [1 ]
机构
[1] Technion Israel Inst Technol, Dept Phys, IL-32000 Haifa, Israel
[2] Delft Univ Technol, Inorgan Chem Lab, NL-2628 BL Delft, Netherlands
关键词
mixed potential; Nafion (R); Ag electrodes on Nafion (R); Pt electrodes on Nafion (R); Pd electrodes on Nafion (R);
D O I
10.1016/S0167-2738(01)00841-4
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
In electrochemical cells based on Nafion (R), exposed to a humid atmosphere that contains oxygen, hydrogen or a mixture of oxygen and hydrogen, the open circuit voltage, V-oc, depends linearly on the logarithm of the concentrations [H-2] and [O-2] in the gas phase. We show, experimentally, that the slope of these relations is significantly higher than in a concentration cell based on a free proton conductor. This was explained before to be due to a mixed potential formed by the oxidation of hydrogen. However, this explanation cannot be applied when one of the reacting gases H-2 or O-2 is missing. We suggest a different explanation that involves reactions that are in equilibrium and others totally blocked. With this mixed equilibrium-non-equilibrium approach (MENEA), we are able to interpret all the experimental results obtained under different conditions. in the analysis of these experiments, we always find a water transference coefficient m similar to 3, as expected for the species H+. (H2O)(m) that transports protons in highly humidified Nafion (R). The explanations are consistent with (a) Ag and Pd catalyzing the absorption of water by Nafion (R), (b) Pt and Pd catalyzing the reaction of oxygen and hydrogen with charged complexes in Nafion (R), and (c) in the absence of oxygen, Ag, Pt and Pd forming an oxide with water. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:205 / 217
页数:13
相关论文
共 28 条
[1]  
BOCKRIS JOM, 1973, MODERN ELECTROCHEMIS, V2, P1104
[2]   ADSORPTION OF HYDROGEN ON PALLADIUM SINGLE-CRYSTAL SURFACES [J].
CONRAD, H ;
ERTL, G ;
LATTA, EE .
SURFACE SCIENCE, 1974, 41 (02) :435-446
[3]   A NOVEL THIN-FILM ELECTROCHEMICAL DEVICE FOR ENERGY-CONVERSION [J].
DYER, CK .
NATURE, 1990, 343 (6258) :547-548
[4]   Trends in the chemical reactivity of surfaces studied by ab initio quantum-dynamics calculations [J].
Eichler, A ;
Hafner, J ;
Gross, A ;
Scheffler, M .
PHYSICAL REVIEW B, 1999, 59 (20) :13297-13300
[5]   ADSORPTION OF OXYGEN ON SILVER SINGLE-CRYSTAL SURFACES [J].
ENGELHARDT, HA ;
MENZEL, D .
SURFACE SCIENCE, 1976, 57 (02) :591-618
[6]   THE INTERACTION OF WATER WITH THE PT(111) SURFACE [J].
FISHER, GB ;
GLAND, JL .
SURFACE SCIENCE, 1980, 94 (2-3) :446-455
[7]   EXPERIMENTAL-DETERMINATION OF THE TRANSPORT NUMBER OF WATER IN NAFION-117 MEMBRANE [J].
FULLER, TF ;
NEWMAN, J .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1992, 139 (05) :1332-1337
[8]  
GABIS IE, 1990, PHYS M MET RUSS JAN, P93
[9]   ADSORPTION OF OXYGEN ON A STEPPED PLATINUM SINGLE-CRYSTAL SURFACE [J].
GLAND, JL ;
KORCHAK, VN .
SURFACE SCIENCE, 1978, 75 (04) :733-750
[10]   THIN-FILM FUEL-CELLS [J].
GOTTESFELD, S .
NATURE, 1990, 345 (6277) :673-673