Tailoring the Icephobic Performance of Slippery Liquid-Infused Porous Surfaces through the LbL Method.

There has been increasing interest in recent years in identifying an ice-removal procedure that is low cost and scalable and consumes a negligible amount of energy in order to prevent catastrophic failures in outdoor structures. One of the potential solutions to the structural problems caused by frigid and icy conditions is the use of slippery liquid-infused porous surfaces (SLIPS) to effect passive ice removal using easy, economical, and energy-free means. This work takes advantage of the highly flexible layer-by-layer (LbL) technology to customize and design surfaces that have a high degree of roughness using negatively and positively charged polyelectrolytes and negatively charged silica nanoparticles (NPs). SEM (scanning electron microscopy) images represent the silica nanoparticles deposition on the surface of the thin film. The roughness of these thin films has been demonstrated by AFM (atomic force microscopy) investigation. The main characteristics of these surfaces are their high contact angle and low water contact angle hysteresis, which is achieved by the fluorinated lubricant that is infused in the pores of the films. The ice adhesion strength of the thin films was measured using a home-built normal mode tensile test in an environmental chamber, which confirmed the icephobicity of the surface as having an adhesion strength of less than 5 kPa, implying that this surface is an excellent candidate for passive removal of ice. The thin films were aged for up to 100 days, and the results showed that the thin film could reduce the ice adhesion strength by 65%, even after this period. The ice adhesion strength of the thin film after icing/deicing cycles showed that 80% of the icephobicity of the thin film had been preserved even after 50 cycles.

Multilayer transfer printing of electroactive thin film composites.

We demonstrate the high fidelity transfer printing of an electroactive polymer nanocomposite thin film onto a conductive electrode. Polyelectrolyte multilayer thin films of thickness ∼200 nm containing 68 vol % Prussian Blue nanoparticles are assembled on a UV-curable photopolymer stamp and transferred in their entirety onto ITO-coated glass creating ∼2.5 µm-wide line patterns with ∼1.25 µm spacing. AFM and SEM are used to investigate pattern fidelity and morphology, while cyclic voltammetry confirms the electroactive nature of the film and electrical connectivity with the electrode. The patterning strategy presented here could be used to pattern electroactive thin films containing a high density of nanoparticles onto individually addressable microelectrodes for a variety of applications ranging from biosensor arrays to flexible electronics.

Layer-by-layer assembled polyaniline nanofiber/multiwall carbon nanotube thin film electrodes for high-power and high-energy storage applications.

Thin film electrodes of polyaniline (PANi) nanofibers and functionalized multiwall carbon nanotubes (MWNTs) are created by layer-by-layer (LbL) assembly for microbatteries or -electrochemical capacitors. Highly stable cationic PANi nanofibers, synthesized from the rapid aqueous phase polymerization of aniline, are assembled with carboxylic acid functionalized MWNT into LbL films. The pH-dependent surface charge of PANi nanofibers and MWNTs allows the system to behave like weak polyelectrolytes with controllable LbL film thickness and morphology by varying the number of bilayers. The LbL-PANi/MWNT films consist of a nanoscale interpenetrating network structure with well developed nanopores that yield excellent electrochemical performance for energy storage applications. These LbL-PANi/MWNT films in lithium cell can store high volumetric capacitance (~238 ± 32 F/cm(3)) and high volumetric capacity (~210 mAh/cm(3)). In addition, rate-dependent galvanostatic tests show LbL-PANi/MWNT films can deliver both high power and high energy density (~220 Wh/L(electrode) at ~100 kW/L(electrode)) and could be promising positive electrode materials for thin film microbatteries or electrochemical capacitors.

Electrochemically controlled swelling and mechanical properties of a polymer nanocomposite.

We present the layer-by-layer assembly of an electroactive polymer nanocomposite thin film containing cationic linear poly(ethyleneimine) (LPEI) and 68 vol % anionic Prussian Blue (PB) nanoparticles, which allow for electrochemical control over film thickness and mechanical properties. Electrochemical reduction of the PB doubles the negative charge on the particles, causing an influx of water and ions from solution to maintain electroneutrality in the film; concomitant swelling and increased elastic compliance of the film result. Reversible swelling upon reduction is on the order of 2-10%, as measured via spectroscopic ellipsometry and electrochemical atomic force microscopy. Reversible changes in the Young's elastic modulus of the hydrated composite film upon reduction are on the order of 50% (from 3.40 to 1.75 GPa) as measured with in situ nanoindentation, and a qualitative increase in viscous contributions to energy dissipation upon redox is indicated by electrochemical quartz crystal microbalance. Electrochemical stimuli maintain a mild operating environment and can be applied rapidly, reversibly, and locally. We maintain that electrochemical control over the swelling and mechanical behavior of polymer nanocomposites could have important implications for responsive coatings of nanoscale devices, including mechanically tunable surfaces to modulate behavior of adherent cells.

Patterned superhydrophobic surfaces: toward a synthetic mimic of the Namib Desert beetle.

The present study demonstrates a surface structure that mimics the water harvesting wing surface of the Namib Desert beetle. Hydrophilic patterns on superhydrophobic surfaces were created with water/2-propanol solutions of a polyelectrolyte to produce surfaces with extreme hydrophobic contrast. Selective deposition of multilayer films onto the hydrophilic patterns introduces different properties to the area including superhydrophilicity. Potential applications of such surfaces include water harvesting surfaces, controlled drug release coatings, open-air microchannel devices, and lab-on-chip devices.

Nanoporosity-driven superhydrophilicity: a means to create multifunctional antifogging coatings.

Multifunctional nanoporous thin films have been fabricated from layer-by-layer assembled silica nanoparticles and a polycation. The resultant multilayer films were found to exhibit both antifogging and antireflection properties. The antifogging properties are a direct result of the development of superhydrophilic wetting characteristics (water droplet contact angle <5 degrees within 0.5 s or less). The nearly instantaneous sheetlike wetting promoted by the superhydrophilic multilayer prevents light scattering water droplets from forming on a surface. The low refractive index of the multilayer film (as low as 1.22) resulting from the presence of nanopores was found to impart excellent antireflection properties. Glass slides coated on both sides with a nanoporous multilayer film exhibited transmission levels as high as 99.8%. Stable superhydrophilic wetting characteristics were obtained only after a critical number of bilayers were deposited onto a surface. The assembly conditions (solution pH and nanoparticle concentration), as well as the choice of nanoparticle size, were found to strongly influence film properties. It is suggested that the superhydrophilic behavior is driven by the rapid infiltration of water into a 3D nanoporous network created under specific assembly conditions.