Proton Exchange Membrane Water Electrolysis Incorporating Sulfo-Phenylated Polyphenylene Catalyst Coated Membranes

被引:8
|
作者
Wang, Xin [1 ]
Mardle, Peter [1 ]
Adamski, Michael [1 ]
Chen, Binyu [1 ]
Holdcroft, Steven [1 ]
机构
[1] Simon Fraser Univ, Dept Chem, Burnaby, BC V5A 1S6, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
FUEL-CELL; COMPOSITE MEMBRANES; PERFORMANCE; DURABILITY; DEGRADATION; HYDROGEN; TEMPERATURE; STABILITY; IONOMERS;
D O I
10.1149/1945-7111/acb643
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Herein, fully hydrocarbon-based ionomer catalyst coated membranes (CCM)s based on sulfo-phenylated polyphenylene biphenyl (sPPB-H+) are evaluated in a proton exchange membrane water electrolyzer cell at 70 degrees C. In conjunction with catalyst layers incorporating Nafion (R) D520 ionomer, sPPB-H+ membranes require a lower applied potential than reference Nafion (R) NR112 recast membranes of equal thickness, e.g., 1.66 V vs 1.75 V at 1 A cm(-2). Initially, sPPB-H+ membranes yield substantially lower gas crossover compared to the CCMs containing NR112 membrane, however, increasing gas crossover and a higher rates of voltage evolution is measured during a stability test at 1 A cm(-2). A reinforced and commercialized membrane of similar chemistry (Pemion (R)) is also evaluated, demonstrating smaller changes to the initial gas crossover owing to higher mechanical stability. Employment of sPPB-H+ as the catalyst layer binder is also investigated, where the highest efficiency for all-sPPB-H+ CCMs is achieved when the anode and cathode ionomer content are 20 wt%, which from electrochemical impedance spectroscopy is predominately attributed to changes in the proton conductivity within the catalyst layer. Despite this advancement, high ionomer swelling and catalyst delamination led to shorter electrolyzer lifetimes for the all hydrocarbon and non fluorinated membrane electrode assembly, informing future ionomer development.
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页数:14
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