Highly durable fuel cell electrodes based on ionomers dispersed in glycerol

被引:69
作者
Kim, Y. S. [1 ]
Welch, C. F. [2 ]
Mack, N. H. [3 ]
Hjelm, R. P. [4 ]
Orler, E. B. [2 ]
Hawley, M. E. [2 ]
Lee, K. S. [1 ]
Yim, S. -D. [1 ]
Johnston, C. M. [1 ]
机构
[1] Los Alamos Natl Lab, Sensors & Electrochem Devices Grp, Los Alamos, NM 87545 USA
[2] Los Alamos Natl Lab, Polymers & Coatings Grp, Los Alamos, NM 87545 USA
[3] Los Alamos Natl Lab, Phys Chem & Appl Spect Grp, Los Alamos, NM 87545 USA
[4] Los Alamos Natl Lab, Los Alamos Neutron Sci Ctr, Los Alamos, NM 87545 USA
关键词
CATALYSTS; DEGRADATION; DURABILITY; SCATTERING; INTERFACE; PEFCS; ELECTROCATALYSTS; ALLOY;
D O I
10.1039/c4cp00496e
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070305 [高分子化学与物理];
摘要
A major, unprecedented improvement in the durability of polymer electrolyte membrane fuel cells is obtained by tuning the properties of the interface between the catalyst and the ionomer by choosing the appropriate dispersing medium. While a fuel cell cathode prepared from aqueous dispersion showed 90 mV loss at 0.8 A cm(-2) after 30000 potential cycles (0.6-1.0 V), a fuel cell cathode prepared from glycerol dispersion exhibited only 20 mV loss after 70000 cycles. This minimum performance loss occurs even though there was an over 80% reduction of electrochemical surface area of the Pt catalyst. These findings indicate that a proper understanding and control of the catalyst-water-ionomer (three-phase) interfaces is even more important for maintaining fuel cell durability in typical electrodes than catalyst agglomeration, and this opens up a novel path for tailoring the functional properties of electrified interfaces.
引用
收藏
页码:5927 / 5932
页数:6
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