Impact of Substrate and Processing on Confinement of Nafion Thin Films

被引:187
作者
Kusoglu, Ahmet [1 ]
Kushner, Douglas [2 ]
Paul, Devproshad K. [3 ]
Karan, Kunal [3 ]
Hickner, Michael A. [2 ]
Weber, Adam Z. [1 ]
机构
[1] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Environm Energy Technol Div, Berkeley, CA 94720 USA
[2] Penn State Univ, Dept Mat Sci & Engn, University Pk, PA 16802 USA
[3] Queens Univ, Dept Chem Engn, Kingston, ON K7L 3N6, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
PROTON CONDUCTION MECHANISM; ELECTROLYTE FUEL-CELLS; X-RAY-SCATTERING; WATER-UPTAKE; CATALYST LAYERS; MONOLAYER FILMS; ADSORBED NAFION; TRANSPORT; MEMBRANE; ANGLE;
D O I
10.1002/adfm.201304311
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Thin films of ion-conducting polymers are an important area of study due to their function in many electrochemical devices and as analogues for interfacial phenomena that occur in bulk films. In this paper, the properties of Nafion, a prototypical ionomer, are investigated as thin films (4 to 300 nm) on carbon, gold, and platinum substrates that are fabricated using different casting methods and thermal histories. Specifically, water uptake, swelling, and morphology are investigated by quartz-crystal microbalance, ellipsometry, and grazing-incidence X-ray scattering to develop structure/property/ processing relationships. For all substrates, as the films' thickness decreased, there is an initial decrease in swelling followed by a subsequent increase for film thicknesses below approximate to 20 nm due to a disordering of the film hydrophilic/hydrophobic structure. Decreased swelling and less structural order is observed on gold for spin-cast films compared to self-assembled films; the opposite effect is observed for films on carbon. The presented systematic data set and analyses represent a thorough study of the behavior of Nafion thin films on model substrates of interest in metal catalyst/carbon electrodes, and these insights help to elucidate the underlying polymer physics and confinement effects in these and related systems.
引用
收藏
页码:4763 / 4774
页数:12
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