Nafion公司
接触角
润湿
材料科学
X射线光电子能谱
化学工程
色散(光学)
薄脆饼
弹性体
椭圆偏振法
膜
分析化学(期刊)
薄膜
化学
复合材料
纳米技术
有机化学
光学
电化学
物理化学
物理
生物化学
电极
工程类
作者
Devproshad K. Paul,Kunal Karan,Aristides Docoslis,Javier B. Giorgi,Joshua M. Pearce
出处
期刊:Macromolecules
[American Chemical Society]
日期:2013-04-22
卷期号:46 (9): 3461-3475
被引量:159
摘要
Self-assembled Nafion films of varying thickness were generated on SiO2 terminated silicon wafer by immersion in Nafion dispersions of different concentrations. The impact of solvent/dispersion media was probed by preparing films from two different types of Nafion dispersions—IPA-diluted dispersion and Nafion-in-water dispersion. The thickness of films was ascertained by three different techniques: variable angle spectroscopic ellipsometry (VASE), atomic force microscopy (AFM), and X-ray photoelectron spectroscopy (XPS). The three techniques yielded consistent nominal thicknesses of 4, 10, 30, 55, 75, 110, 160, and 300 nm for films self-assembled from IPA-diluted Nafion dispersions of concentrations 0.1, 0.25, 0.5, 1.0, 1.5, 2.0, 3.0, and 5.0 wt %, respectively. Films generated from 0.25–5.0 wt % Nafion-in-water dispersions generated comparable thicknesses. An interesting finding of our work is the observation of bimodal surface wettability, investigated by water contact angle. The sub-55 nm films were found to exhibit hydrophilic surface whereas the thicker films showed hydrophobic surface similar to those reported for Nafion membranes. Employing XDLVO theory, surface energies of the hydrophobic, 160 nm film was found to be similar to that reported for Nafion membrane whereas those for the hydrophilic 4 nm film yielded high electron-accepting/proton-donating parameters resulting in an enhanced surface polarity. It can be concluded that the structure and properties of the ultrathin (<55 nm) Nafion films are distinct from those of the thicker (but still submicrometer) films, which are likely similar to those of the well-studied Nafion membranes. No significant effect of dispersion type was observed for 10–300 nm thick films.
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