Influence of thermal post-curing on the degradation of a cross-linked polybenzimidazole-based membrane for high temperature polymer electrolyte membrane fuel cells

被引:29
作者
Ossiander, T. [1 ]
Perchthaler, M. [2 ]
Heinzl, C. [1 ]
Scheu, C. [1 ]
机构
[1] Univ Munich, Dept Chem, D-81377 Munich, Germany
[2] Graz Univ Technol, Inst Chem Engn & Environm Technol, A-8010 Graz, Austria
关键词
High temperature polymer electrolyte membrane; Fuel cell; Polybenzimidazole; Thermal post-curing; Degradation mechanisms; PHOSPHORIC-ACID; PBI MEMBRANES; REDUCTION; LINKING;
D O I
10.1016/j.jpowsour.2014.04.158
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 lifetime stability of membranes is one of the main requirements regarding reliability of high temperature polymer electrolyte membrane fuel cells. The present work has improved durability under cycled operation by thermal post-curing of cross-linked polybenzimidazole (PBI)-based membranes. The membranes were dried over 1, 2 and 3 h at 250 degrees C under air. Ex-situ experiments proved an increase in stability by post-curing. The liquid uptake and swelling in phosphoric acid increased with longer curing periods. The effect of thermal treatments on cycle stability, lifetime and begin-of-life performance of the membrane electrode assemblies (MEAs) was investigated. Longer post-curing periods of the membranes had no influence on the MEAs' begin-of-life performance and constant current behavior over 2300 h. However, the 3 h post-cured MEAs showed enhanced cycle stability. Post-mortem analysis was carried out to identify the occurring degradation mechanisms. While a significant loss of phosphoric acid and a reduction of electrochemical surface activity on the cathode were observed for both post-cured MEAs, the 3 h dried membrane sample had a significantly higher resistance against pinhole formation during the long term test. Altogether, this work presents thermal post-curing as a promising method for the reduction of degradation determining effects in fuel cell membranes. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:323 / 328
页数:6
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