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      Transparent, abrasion-insensitive superhydrophobic coatings for real-world applications

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          Abstract

          Superhydrophobic surfaces and surface coatings are of high interest for many applications in everyday life including non-wetting and low-friction coatings as well as functional clothing. Manufacturing of these surfaces is intricate since superhydrophobicity requires structuring of surfaces on a nano- to microscale. This delicate surface structuring makes most superhydrophobic surfaces very sensitive to abrasion and renders them impractical for real-life applications. In this paper we present a transparent fluorinated polymer foam that is synthesized by a simple one-step photoinitiated radical polymerization. We term this material “Fluoropor”. It possesses an inherent nano-/microstructure throughout the whole bulk material and is thus insensitive to abrasion as its superhydrophobic properties are not merely due to a thin-layer surface-effect. Due to its foam-like structure with pore sizes below the wavelength of visible light Fluoropor appears optically transparent. We determined contact angles, surface energy, wear resistance and Vickers hardness to highlight Fluoropor’s applicability for real-word applications.

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          Candle soot as a template for a transparent robust superamphiphobic coating.

          Coating is an essential step in adjusting the surface properties of materials. Superhydrophobic coatings with contact angles greater than 150° and roll-off angles below 10° for water have been developed, based on low-energy surfaces and roughness on the nano- and micrometer scales. However, these surfaces are still wetted by organic liquids such as surfactant-based solutions, alcohols, or alkanes. Coatings that are simultaneously superhydrophobic and superoleophobic are rare. We designed an easily fabricated, transparent, and oil-rebounding superamphiphobic coating. A porous deposit of candle soot was coated with a 25-nanometer-thick silica shell. The black coating became transparent after calcination at 600°C. After silanization, the coating was superamphiphobic and remained so even after its top layer was damaged by sand impingement.
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            Moving superhydrophobic surfaces toward real-world applications

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              Hydrophilic and superhydrophilic surfaces and materials

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                Author and article information

                Contributors
                bastian.rapp@kit.edu
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                8 November 2017
                8 November 2017
                2017
                : 7
                : 15078
                Affiliations
                [1 ]ISNI 0000 0001 0075 5874, GRID grid.7892.4, Institute of Microstructure Technology (IMT), Karlsruhe Institute of Technology (KIT), Hermann-von-Helmholtz-Platz 1, ; 76344 Eggenstein-Leopoldshafen, Germany
                [2 ]ISNI 0000 0001 0075 5874, GRID grid.7892.4, Institute for Applied Materials - Computational Materials Science (IAM-CMS), Karlsruhe Institute of Technology (KIT), Engelbert-Arnold-Str. 4, ; 76131 Karlsruhe, Germany
                Author information
                http://orcid.org/0000-0002-3955-0291
                Article
                15287
                10.1038/s41598-017-15287-8
                5678135
                29118407
                0c96eeb6-f262-4c9b-8399-870a8c5f78cf
                © The Author(s) 2017

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 1 September 2017
                : 24 October 2017
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