Smart responsive surfaces switching reversibly between super-hydrophobicity and super-hydrophilicity

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Smart responsive surfaces switching reversibly between super-hydrophobicity and super-hydrophilicity

Authors: Fan Xia, Ying Zhu, Lin Feng and Lei Jiang

Soft Matter, 2009, 5, 275–281

Soft matter keywords

superhydrophobicity, photowetting, electrowetting, thermowetting, pH-response, mechanowetting, multiresponsive surfaces

By Alex Epstein

Abstract from the original paper

Super-hydrophilicity and super-hydrophobicity are fundamentally opposite properties of special wettability, which are governed by surface chemical composition and surface roughness. Smart responsive surfaces switching reversibly between super-hydrophobicity and super-hydrophilicity can be effectively fabricated by modification of stimuli-responsive materials on rough surfaces. The externally applied stimuli include light irradiation, electrical potential, temperature, pH or selected solvents, and mechanical forces. Such surfaces with controllable wettability are of great importance to both fundamental research and practical applications.

Soft matters

The authors, who have written a considerable body of papers on controllable wettability, discuss five principal systems of surface wetting control. There is clearly a good deal of progress to date in reversibly switching between superhydophobic and philic surface states. I found this paper interesting because it explains the different approaches to control surface chemistry and topography; the surface is not a black box, and its effect on the contact angle can be understood and exploited.


As photogeneration increases carrier concentration in semiconductors, so do photo-responsive surfaces change their surface chemistry in the presence of UV radiation. The most well known class of photo-responsive materials are inorganic semiconductor oxides such as titania, zinc oxide, vanadium oxide, etc. These materials are normally hydrophobic, so texturing them with submicron roughness, as seen in Fig. 1, amplifies them to superhydrophobic. However, exposure of the surfaces to UV light renders them hydrophilic, and their roughness collaborates to give complete wetting, as predicted by the Wenzel relation. Now storage in the dark restores superhydrophobicity! As seen in Fig. 1, the contact angle was shown to change reversibly from 0 to 160 deg for at least 5 cycles without degradation.

The generation of superhydrophilicity by exposure to UV light is closely related to the preferential adsorption of water on photogenerated surface defect sites. UV exposure generates electron−hole pairs in, e.g., V2O5. The holes react with lattice oxygen, leading to the creation of surface oxygen vacancies, while the electrons react with lattice metal ions, inducing conversion of V5+ sites to V3+ defect sites. Hydroxyl adsorption on the defect sites is kinetically more favorable than oxygen adsorption, which leads to dissociative adsorption of water molecules at these sites. This renders the V2O5 films hydrophilic. [1]

Some organic compounds can also show the photoresponsive transition. Azobenzene and spiropyran molecules are typical examples. Irradiation by UV or visible light causes a cis-trans conformation change or cleavage of a C-O bond, respectively. The point is that the molecules switch between polar and nonpolar forms in response to light and switch back in the dark.


Electric control is desirable because it is a simple and familiar type of input.


pH and Solvent


Multiresponsive and Common Theme

Fig. 1 (a) Water-drop profiles for the nano-structured V2O5. (b) SEM of a rose-garden-like nanostructure V2O5 substrate. (c) XPS of the O 1s level before and after UV irradiation. (d) Reversible wettability transitions through UV exposure and dark storage, respectively.
Fig. 2 (a) SEM image of the nanograss substrate. (b) Demonstration of electrically induced reversible transitions between different wetting states on a nanostructured substrate. (1) With no voltage applied. (2) With the application of about 35 V. (3) With a short pulse of electrical current.
Fig. 3 (a) SEM image of the nanostructures on rough substrate modified with PNIPAAm. (b) Water drop profile for responsive surface at 25 C and 40 C. (c) Diagram of reversible formation of intermolecular hydrogen bonding between PNIPAAm chains and water molecules (left) and intramolecular hydrogen bonding between C]O and N–H groups in PNIPAAm chains (right) below and above the LCST, which is considered to be the molecular mechanism of the thermally responsive wettability of a PNIPAAm thin film. (d) CAs in at two different temperatures 20 C and 40 C for PNIPAAm-modified rough substrate.
Fig. 4 SEM images of deposited gold structures: (a) micro-scale gold structures, (b) magnified image of the gold clusters. Photographs of (c) acid and (d) base droplet applied on the surface. The CA of the acid droplet is 154 deg and the basic droplet will spread out on the surface gradually.
Fig. 5 Reversibly change in structure and wettability of the triangular polyamide film during extension and unloading.


1. UV-Driven Reversible Switching of a Roselike Vanadium Oxide Film between Superhydrophobicity and Superhydrophilicity. Ho Sun Lim,, Donghoon Kwak,, Dong Yun Lee,, Seung Goo Lee, and, Kilwon Cho. Journal of the American Chemical Society 2007 129 (14), 4128-4129