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Microscopic insights on the degradation of a PEM water electrolyzer with ultra-low catalyst loading
被引:91
作者:
Yu, Haoran
[1
,2
]
Bonville, Leonard
[2
]
Jankovic, Jasna
[2
,3
]
Maric, Radenka
[1
,2
,3
]
机构:
[1] Univ Connecticut, Dept Chem & Biomol Engn, 191 Auditorium Rd,Unit 3222, Storrs, CT 06269 USA
[2] Univ Connecticut, Ctr Clean Energy Engn, 44 Weaver Rd,Unit 5233, Storrs, CT 06269 USA
[3] Univ Connecticut, Dept Mat Sci & Engn, 97 North Eagleville Rd, Storrs, CT 06269 USA
关键词:
Proton exchange membrane water electrolysis;
Membrane electrode assembly;
Stability;
Degradation;
OXYGEN EVOLUTION ACTIVITY;
ENERGY CARRIER;
MEMBRANE;
STABILITY;
IRIDIUM;
HYDROGEN;
PERFORMANCE;
DISSOLUTION;
FUEL;
ELECTROCATALYSTS;
D O I:
10.1016/j.apcatb.2019.118194
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 present work aims for a comprehensive understanding of the degradation of proton exchange membrane water electrolyzer (PEMWE) with a low catalyst loading of 0.3 mg cm(-2) Pt and 0.08 mg cm(-2) Ir after a long-term test of 4500 h at 1.8 A cm(-2). For the first time, the mechanism of cathode degradation is proposed using established physical models from two aspects: (1) Pt dissolution from nanoparticles and (2) Pt dissolution due to rapid Pt oxide reduction at the start of operation. As Ir dissolves and migrates through the membrane, Pt-Ir precipitates are formed in the membrane. Furthermore, iridium dissolution and subsequent re-deposition on the cathode constitute a major portion (42%) of the anode catalyst loss. The overall picture of degradation mechanisms and the distribution of platinum and iridium across the membrane electrode assembly (MEA) are provided.
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页数:13
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