The Control and Effect of Pore Size Distribution in AEMFC Catalyst Layers

被引:67
作者
Britton, Benjamin [1 ]
Holdcroft, Steven [1 ]
机构
[1] Simon Fraser Univ, Dept Chem, Burnaby, BC V5A 1S6, Canada
基金
加拿大创新基金会;
关键词
ANION-EXCHANGE MEMBRANES; ALKALINE FUEL-CELLS; HYDROXIDE-CONDUCTING POLYMER; ELECTROCHEMICAL DEVICES; PERFORMANCE; ELECTRODE; TETRAHYDROFURAN; MICROSTRUCTURE; COPOLYMERS; IONOMERS;
D O I
10.1149/2.0421605jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Catalyst ink for anion-exchange catalyst coated membranes based on FuMA-Tech FAA-3 membranes and ionomer typically requires high-boiling solvents. Here, we investigate the disproportionate effect of even small quantities of high-boiling solvent in the catalyst ink on the catalyst layer microstructure. High porosity in themesoporous regime, 20-100 nm, is found to be an essential characteristic of effective anion-exchange catalyst layers for increasing membrane hydroxide ion conductivity and reducing mass-transport losses. High porosity in the nanoporous regime (<20 nm pore diameter) facilitates improvements in the kinetic region of polarization curves at the expense of mass-transport losses. New strategies are introduced to improve the control of distribution of pore sizes in the catalyst layer and to increase the mesoporosity. Beginning-of-life power densities for O-2/H-2 anion exchange membrane fuel cells (AEMFCs), under zero backpressure, were accordingly increased from 276 to 428 mW . cm(-2), placing it among the highest AEMFC power densities reported in the literature under the conditions studied, representing a significant improvement over previously reported performances for FAA-3. The study highlights a need to develop anion-exchange solid polymer ionomers soluble in low-boiling solvents for preparing catalyst inks, and a more rigorous evaluation of porosimetry data and catalyst layer preparation methods for AEMFCs. (C) The Author(s) 2016. Published by ECS. All rights reserved.
引用
收藏
页码:F353 / F358
页数:6
相关论文
共 47 条
[1]   Dielectric constants of some organic solvent-water mixtures at various temperatures [J].
Akerlof, G .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1932, 54 :4125-4139
[2]   Best Practices for Investigating Anion Exchange Membrane Suitability for Alkaline Electrochemical Devices: Case Study Using Quaternary Ammonium Poly(2,6-dimethyl 1,4-phenylene)oxide Anion Exchange Membranes [J].
Arges, Christopher G. ;
Wang, Lihui ;
Parrondo, Javier ;
Ramani, Vijay .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2013, 160 (11) :F1258-F1274
[3]  
Biros J., 1972, COLLECT CZECH CHEM C, V37, P3960
[4]   The synthesis and characteristic of an anion conductive polymer membrane for alkaline anion exchange fuel cells [J].
Cao, Yuan-Cheng ;
Wang, Xu ;
Scott, Keith .
JOURNAL OF POWER SOURCES, 2012, 201 :226-230
[5]   Development and electrochemical studies of membrane electrode assemblies for polymer electrolyte alkaline fuel cells using FAA membrane and ionomer [J].
Carmo, Marcelo ;
Doubek, Gustavo ;
Sekol, Ryan C. ;
Linardi, Marcelo ;
Taylor, Andre D. .
JOURNAL OF POWER SOURCES, 2013, 230 :169-175
[6]   Temperature dependent dielectric relaxation study of Tetrahydrofuran in Methanol and Ethanol at microwave frequency using Time Domain Technique. [J].
Chaudhari, A ;
Khirade, P ;
Singh, R ;
Helambe, SN ;
Narain, NK ;
Mehrotra, SC .
JOURNAL OF MOLECULAR LIQUIDS, 1999, 82 (03) :245-253
[7]   Effect of Organic Solvents on the Pore Structure of Catalyst Layers in Polymer Electrolyte Membrane Fuel Cells [J].
Chisaka, Mitsuharu ;
Matsuoka, Eitaro ;
Daiguji, Hirofumi .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2010, 157 (08) :B1218-B1221
[8]   Polymeric materials as anion-exchange membranes for alkaline fuel cells [J].
Couture, Guillaume ;
Alaaeddine, Ali ;
Boschet, Frederic ;
Ameduri, Bruno .
PROGRESS IN POLYMER SCIENCE, 2011, 36 (11) :1521-1557
[9]   The Effect of Noncovalent Interactions on the HOR, ORR, and HER on Ru, Ir, and Ru0.50Ir0.50 Metal Surfaces in Alkaline Environments [J].
Danilovic, N. ;
Subbaraman, Ram ;
Strmcnik, D. ;
Paulikas, A. P. ;
Myers, D. ;
Stamenkovic, V. R. ;
Markovic, N. M. .
ELECTROCATALYSIS, 2012, 3 (3-4) :221-229
[10]   New insights into the electrochemical hydrogen oxidation and evolution reaction mechanism [J].
Durst, J. ;
Siebel, A. ;
Simon, C. ;
Hasche, F. ;
Herranz, J. ;
Gasteiger, H. A. .
ENERGY & ENVIRONMENTAL SCIENCE, 2014, 7 (07) :2255-2260