Understanding Platinum Ionomer Interface Properties of Polymer Electrolyte Fuel Cells

被引:6
|
作者
Qi, Yongzhen [1 ]
Morimoto, Yu [2 ]
Shibata, Masao Suzuki [3 ]
Gao, Ziliang [2 ,4 ]
Sabarirajan, Dinesh C. [5 ]
Haug, Andrew T. [6 ]
Zenyuk, Iryna, V [1 ,2 ,3 ]
机构
[1] Univ Calif Irvine, Dept Mech & Aerosp Engn, Irvine, CA 92717 USA
[2] Univ Calif Irvine, Adv Power & Energy Program, Irvine, CA 92717 USA
[3] Univ Calif Irvine, Dept Chem & Biomol Engn, Irvine, CA 92717 USA
[4] Xi An Jiao Tong Univ, State Key Lab Multiphase Flow Power Engn, Int Res Ctr Renewable Energy, Xian 710049, Shaanxi, Peoples R China
[5] Tufts Univ, Dept Mech Engn, Medford, MA 02155 USA
[6] 3M Co, 3M Ctr, St Paul, MN USA
关键词
ACID IONOMERS; CO; ADSORPTION; PT(111); DISPLACEMENT; PERFORMANCE; SURFACE;
D O I
10.1149/1945-7111/ac774f
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
A well-designed cathode catalyst layer with optimal ionomer distribution is critical to minimizing amount of Platinum (Pt) content in polymer electrolyte fuel cells (PEFCs). The impact of Pt loading, ionomer content and carbon support types on the catalyst/ ionomer interface were also investigated at dry and wet conditions. Higher Pt loadings resulted in higher double layer capacity (C-dl) and similar electrochemical surface area (ECSA) due to well dispersed ionic phase material. Higher ionomer content resulted in higher ionic conductivity but also showed similar SO3- group coverage. High surface area (HSA) carbon support had larger ECSA and C(dl )at both dry and wet conditions, as less agglomerated Pt was well dispersed in the meso-pores of the support. Lower SO3- group coverages were observed for HSA carbon than for Vulcan carbon due to Pt particles being buried within the porous HSA carbon support. The effect of cell conditioning and voltage recovery on the PEFC cathode catalyst layer was shown to have minimal impact on SOT group coverage despite a decrease in Cap and ECSA due to the size increase of Pt particles. At dry condition, a significant increases in SO3- group coverage were observed for all MEAs due to higher adsorptivity of ionomer in dry conditions. (C) 2022 The Author(s). Published on behalf of The Electrochemical Society by IOP Publishing Limited.
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页数:9
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