Effect of Organic Solvents on Catalyst Layer Structure in Polymer Electrolyte Membrane Fuel Cells

被引:23
|
作者
Chisaka, Mitsuharu [1 ]
Daiguji, Hirofumi [1 ]
机构
[1] Univ Tokyo, Grad Sch Frontier Sci, Inst Environm Studies, Chiba 2778563, Japan
基金
日本学术振兴会;
关键词
carbon; catalysts; electrochemical electrodes; organic compounds; platinum; porosity; proton exchange membrane fuel cells; voltammetry (chemical analysis); PLATINUM LOADING ELECTRODES; GAS-DIFFUSION ELECTRODES; OXYGEN REDUCTION; ULTRA-LOW; PERFORMANCE; FILM; ELECTROCATALYSIS; ALLOYS; PEMFC; MEAS;
D O I
10.1149/1.3000592
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The effect of an organic solvent contained in a catalyst ink on the catalyst layer structure was revealed by measuring the porosity and thickness of catalyst layers in the decal method to fabricate membrane electrode assemblies (MEAs) in polymer electrolyte membrane fuel cells. In this study, ethylene glycol and propylene glycol were used as organic solvents. The pore volume of the catalyst layer fabricated from a catalyst ink containing ethylene glycol (CL(EG)) was smaller than that containing propylene glycol (CL(PG)) near the peak pore diameter of 54-66 nm, suggesting the intrusion of perfluorosulfonate-ionomer into the space between carbon black-supported platinum (Pt-C) particles could reduce the pore volume and extend the active reaction area of CL(EG) compared with CL(PG). The thickness of CL(PG) was 1.3 times larger than that of CL(EG) at a fixed platinum loading, m(Pt), suggesting mass transport could restrict the cell performance of CL(EG) compared with CL(PG). The expectations from these two structural analyses were verified by measuring the cyclic voltammograms and current density vs voltage (i-V) curves of a single cell for MEAs fabricated from catalyst inks containing either ethylene glycol or propylene glycol with various m(Pt).
引用
收藏
页码:B22 / B26
页数:5
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