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As compared to superhydrophobic surfaces, the challenge to obtain superoleophobic properties, surfaces against low-surface-tension probe liquids such as hexadecane, is very important because of their high tendency to wet. From the molecular design of the monomer, it is possible to obtain in one step superoleophobic surfaces by electrodeposition. Hence, we report the synthesis and the characterization of an original series of fluorinated 3,4-ethylenedioxypyrrole (EDOP) derivatives. The electrodeposited polymer films are characterized by contact angle measurements (static and dynamic with various probe liquids), optical profilometry, and scanning electron microscopy. In the view toward reaching superoleophobic properties, a common approach is to increase the number of fluoromethylene units of the surface post-treatment agent. Here, surprisingly, it is possible, in one step, to reach more efficient antioil surface properties by decreasing the length of the fluorinated tail (F-octyl to F-hexyl). This fact can be explained by a double scale of structuration (micro and nano) induced using only F-hexyl tails.

International audienceIn order to produce extremely high oleophobic properties with a low fluorine content, long dodecyl spacers were introduced between a polymer and fluorinated chains in order to reduce the mobility of the fluorinated chains, especially short perfluorobutyl (F-butyl) chains. We report the synthesis and characterization of electrodeposited polymer surfaces obtained from original fluorinated 3,4-ethylenedioxypyrrole (EDOP) derivatives. Semi-fluorinated chains of three different lengths (F-octyl: PEDOPC12F8, F-hexyl: PEDOPC12F6 and F-butyl: PEDOPC12F4) were grafted to EDOP and separated with a n-dodecyl chain in order to reduce the mobility of F-butyl chains. For the first time, a surprisingly high contact angle of 138u was measured with hexadecane on PEDOPC12F4, although F-octyl tails are necessary to produce robust superoleophobic surfaces. By producing smooth surfaces, we successfully separate the influence of the intrinsic hydro- and oleophobicity and the surface structuration on the static contact angles of water and hexadecane. Here, the surface structuration increases the contact angle of hexadecane by 90u for PEDOPC12F4. The Cassie-Baxter equation predicts a porosity of 84.5% between the surface and a hexadecane droplet