Issue 43, 2014

Controllable wettability and adhesion on bioinspired multifunctional TiO2 nanostructure surfaces for liquid manipulation

Abstract

Hierarchical surfaces with specific topographical morphology and chemical components can be found on many living creatures in nature. They offer special wettability and adhesion (sliding, sticky or patterned superhydrophobic surfaces), a functional platform for microfluidic management and other biological functions. Inspired by their precise arrangement of structures and surface components, we described a facile one-step electrochemical technique to create dual-scale hierarchical anatase TiO2 structures with the combination of pinecone-like micro-particle upper layers and dense-stacked nanoparticle bottom layers in a large scale. The as-prepared TiO2 films display environment-responsive wettability with good dynamical stability. Extremely high contrast of adhesion (2.5–170 μN) can be realized by simply adjusting the physical structures (anodizing voltage and electrolyte concentration dependent) to control the solid–liquid contact state (from “Rose” to “Lotus” state). In addition, erasable and rewritable patterned superhydrophobic TiO2 films were constructed for a versatile platform for microfluidic management. In a proof-of-concept study, robust super-antiwetting films for on-demand droplet separation, mixing and transportation under an ambient atmosphere or an underwater environment, and patterned superhydrophobic surfaces for liquid self-assembling or anti-counterfeiting marks were demonstrated.

Graphical abstract: Controllable wettability and adhesion on bioinspired multifunctional TiO2 nanostructure surfaces for liquid manipulation

Supplementary files

Article information

Article type
Paper
Submitted
08 Aug 2014
Accepted
09 Sep 2014
First published
10 Sep 2014

J. Mater. Chem. A, 2014,2, 18531-18538

Author version available

Controllable wettability and adhesion on bioinspired multifunctional TiO2 nanostructure surfaces for liquid manipulation

J. Huang, Y. Lai, L. Wang, S. Li, M. Ge, K. Zhang, H. Fuchs and L. Chi, J. Mater. Chem. A, 2014, 2, 18531 DOI: 10.1039/C4TA04090B

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