Effect of interface on surface morphology and proton conduction of polymer electrolyte thin films

被引:44
作者
Ohira, Akihiro [1 ,2 ]
Kuroda, Seiichi [2 ]
Mohamed, Hamdy F. M. [2 ]
Tavernier, Bruno [2 ]
机构
[1] Natl Inst Adv Ind Sci & Technol, Res Inst Ubiquitous Energy Devices, Ikeda, Osaka 5638577, Japan
[2] Technol Res Assoc, Fuel Cell Cutting Edge Res Ctr FC Cub, Koto Ku, Tokyo 1350064, Japan
关键词
CATALYST LAYERS; WATER SORPTION; NAFION; MEMBRANES; AFM; TRANSPORT;
D O I
10.1039/c3cp51136g
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
To understand the relationship between surface morphology and proton conduction of polymer electrolyte thin films, perfluorinated ionomer Nafions thin films were prepared on different substrates such as glassy carbon (GC), hydrophilic-GC (H-GC), and platinum (Pt) as models for the ionomer film within a catalyst layer. Atomic force microscopy coupled with an electrochemical (e-AFM) technique revealed that proton conduction decreased with film thickness; an abrupt decrease in proton conductance was observed when the film thickness was less than ca. 10 nm on GC substrates in addition to a significant change in surface morphology. Furthermore, thin films prepared on H-GC substrates with UV-ozone treatment exhibited higher proton conduction than those on untreated GC substrates. However, Pt substrates exhibited proton conduction comparable to that of GCs for films thicker than 20 nm; a decrease in proton conduction was observed at similar to 5 nm thick film but was still much higher than for carbon substrates. These results indicate that the number of active proton-conductive pathways and/or the connectivity of the proton path network changed with film thickness. The surface morphology of thinner films was significantly affected by the film/substrate interface and was fundamentally different from that of the bulk thick membrane.
引用
收藏
页码:11494 / 11500
页数:7
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