Sliding of water droplets on smooth hydrophobic silane coatings with regular triangle hydrophilic regions.

The effect of the triangular pinning region on the sliding of water droplets on the smooth hydrophobic surface was investigated. Smooth hydrophobic silane coatings with various regular triangle hydrophilic regions were prepared using photolithography and octadecyltrimethoxysilane (ODS). The hydrophilic area in the surfaces was aligned hexagonally with a constant area fraction. Thereby water contact angles of the coatings were almost equivalent. The water droplet sliding velocity increased continuously with increasing pattern size. Anisotropic sliding velocity was observed on the surface, suggesting different pinning effects. The sliding motion of water droplets on the gradient surface with changing hydrophilic region size deflects against the downward direction. The deflection length depends on the direction of triangle hydrophilic regions and the initial sliding position. These results demonstrate that control of the sliding velocity while sustaining the static contact angle is feasible by designing the shape and alignment of chemical heterogeneity.

Preparation and photocatalytic activity of robust titania monoliths for water remediation.

TiO(2) monoliths were prepared, characterized, and evaluated for photocatalytic performance. The TiO(2) monoliths were found to have an interconnected void lattice and a bimodal porous structure with macropores and mesopores after calcination at 500-700 °C. Monoliths calcined at 500 °C had high specific surface area (93.1 m(2)/g) and porosity (68%), which were maintained after calcination at 700-1100 °C (51-46%). The calcined monoliths had relatively high Vickers hardness (∼104) despite their porous structure. Monoliths calcined at 500 and 700 °C exhibited high performance for methylene blue decolorization because of their high specific surface area.

Mesoporous TiO2 core-shell spheres composed of nanocrystals with exposed high-energy facets: facile synthesis and formation mechanism.

A facile new method that combines electrospray and hydrothermal treatment is used to prepare mesoporous core-shell TiO(2) spheres with high specific surface areas and high pore volumes. Interestingly, the resulting TiO(2) spheres are composed of anatase TiO(2) nanocrystals with exposed step-like {001} and smooth {010} facets. The percentage of exposed {001} facets can be adjusted by changing the experimental parameters used in the electrospray and hydrothermal treatment processes, such as the contents of poly(N-vinyl-2-pyrrolidone) and acetic acid. The combination of high specific surface area (>100 m(2) g(-1)), high pore volume (>0.30 cm(3) g(-1)), useful pore size (10-15 nm), spherical core-shell structure, and exposed high energy facets makes these TiO(2) spheres an important candidate for use in many photoelectrochemical applications. The formation mechanism of the mesoporous TiO(2) spheres is also studied. The great advantage of this method is that interesting and complicated mesoporous superstructures can be prepared using electrospray technology.

Photocatalytic activity and related surface properties of transparent ZnO films prepared by a low-temperature aqueous route.

Transparent ZnO were prepared using solutions with various trisodium citrate concentrations by a spin-spray method at 90°C. The morphological and structural characteristics, as well as photocatalytic activity of the resulting ZnO films were examined with respect to the added trisodium citrate concentration. Photocatalytic activities of the ZnO films were evaluated from photodecomposition of methylene blue (MB) in aqueous solution. With increasing citrate concentrations, the ZnO films came to have higher transmittances in visible region but lower MB decomposition rate. Both high transmittance and high photocatalytic activity were achieved in the ZnO film prepared in the citrate concentration of 0.5 mm. The possible mechanism for the difference in photocatalytic activity by the samples prepared with the various concentrations of citrate was discussed from the viewpoint of film texture, crystal orientation and surface chemical state.

Preparation of TiO2 thin films using water-soluble titanium complexes and their photoinduced properties.

Titanium dioxide thin films were prepared by using four water-soluble titanium complexes of titanium-lactate, tartalate, malate and salicylate complex solutions. The crystalline phases detected in the films were anatase. The surface microstructures of the four film samples were different in their grain sizes. Photocatalytic decomposition activity of the four films was almost the same, but their photoinduced hydrophilicities were different. The film prepared using titanium-salicylate complex exhibited lower hydrophilic conversion rate than the other films. Grain size and stress yielded to the film are considered to be important factors on the photoinduced hydrophilicity.

Sliding of water droplets on hydrophobic surfaces with various hydrophilic region sizes.

Four patterned surfaces with hydrophilic areas of different sizes were prepared using photolithography with a smooth octadecyltrimethoxysilane (ODS) hydrophobic coating. The hydrophilic area in the surfaces was aligned hexagonally with a constant area fraction. The sliding angle and contact angle hysteresis of the water droplets increased concomitantly with increasing pattern size. The increase of the contact line distortion between defects at the receding side plays an important role in this trend. The droplet sliding velocity also increased concomitantly with increasing pattern size. This trend was simulated by a simple flow model. The contribution of the interface between the ODS region and the hydrophilic area was deduced from this trend. This study demonstrated the different size dependency of the chemical surface defects for sliding behavior between the critical moment at which a droplet slides down and the period when a droplet is sliding.

Antireflection and self-cleaning properties of a moth-eye-like surface coated with TiO2 particles.

Poly(ethylene terephthalate) (PET) films with a moth-eye-like surface are coated with TiO(2) particles to form self-cleaning antireflective films. The use of a TiO(2) suspension of high concentration to coat the PET surface produces a thicker TiO(2) layer with smaller pores, whereas a low concentration of a TiO(2) suspension gives a thinner layer of TiO(2) with larger pores. The PET films coated with TiO(2) particles exhibit a high transmittance of 76-95% and almost no absorption in the range of 400-800 nm. The PET films coated with a TiO(2) suspension with a concentration of ≥2 vol % exhibit superhydrophilicity after irradiation with UV light. After irradiation, the superhydrophilic nature is retained for at least 18 days. The TiO(2)-coated PET films showed the ability to decompose methylene blue under UV irradiation.

UV/thermally driven rewritable wettability patterns on TiO2-PDMS composite films.

Composite films of TiO2 and polydimethylsiloxane (PDMS) are prepared by a sol-gel method, cured with UV irradiation, and then treated in hot water to crystallize the TiO2 in the film. The presence of anatase TiO2 contributes to the photoinduced superhydrophilicity of the film under UV irradiation. Contact angle studies reveal that the TiO2-PDMS composite film recovers its original hydrophobic state. Hydrophobic-superhydrophilic patterns are successfully formed on the films. The wettability patterns can be erased by UV irradiation and thermal treatment. New wettability patterns can be reconstructed, demonstrating that the film exhibits rewritable wettability without the need for organic chemicals.

Effect of dew condensation on the wettability of rough hydrophobic surfaces coated with two different silanes.

Dew condensation effects on the wettability of rough and smooth coatings of two fluoroalkylsilanes (FAS3 and FAS17) were investigated by controlling the temperature. Contact angles of the coatings decreased concomitantly with decreasing surface temperature. Inflection points in the temperature dependence of contact angles were observed at the dew point. They were attributable to the change of the interfacial free energy of the solid-gas interface by water adsorption. The contact angle decrease suggested a mode transition from Cassie to Wenzel on the rough surface, and resulted from the surface wettability change and the increase of the condensation amount of water. The contact angle change by increasing temperature from -6 degrees C revealed that the Wenzel mode is more stable than Cassie's mode.

Water droplets' internal fluidity during horizontal motion on a superhydrophobic surface with an external electric field.

On a superhydrophobic surface, the internal fluidity of water droplets with different volumes (15, 30 microL) and their horizontal motion in an external electric field were evaluated using particle image velocimetry (PIV). For driving of water droplets on a superhydrophobic coating between parallel electrodes, it was important to place them at appropriate positions. Droplets moved with slipping. Small droplets showed deformation that is more remarkable. Results show that the dielectrophoretic force induced the initial droplet motion and that the surface potential gradient drove the droplets after reaching the middle point between electrodes.

Evaporation behavior of microliter- and sub-nanoliter-scale water droplets on two different fluoroalkylsilane coatings.

The evaporation behavior of microliter (2.0 microL) and subnanoliter (0.8 nL) scale water droplets was investigated on two smooth hydrophobic and hydrophilic fluoroalkylsilane coatings prepared using chemical vapor deposition. The contact angle was constant in the second stage of evaporation for a 2.0 microL droplet on the hydrophobic coating, but it was slightly decreased in the case of a 0.8 nL droplet. The contact angle decreased gradually in the same stage of evaporation for a 2.0 microL droplet on the hydrophilic coating, but it was almost constant for a 0.8 nL droplet. These differences in evaporation behavior are expected to originate from the differences of their magnitudes and signs of line tension.

Sliding of water droplets on the superhydrophobic surface with ZnO nanorods.

In this study, we prepared various superhydrophobic surfaces using ZnO nanorod arrays (ZnO-NR) of different diameters. The contact angle was equivalent to the calculated value if it is assuming that the topmost surface of the rods is a solid-liquid contact area. On the superhydrophobic ZnO-NR surfaces, the 5 microL water droplets slid down by constant acceleration motion. Sliding acceleration was governed by the solid area fraction. The resistance force of the actual measurement was consistent with that calculated using the model.

Evaporation and sliding of water droplets on fluoroalkylsilane coatings with nanoscale roughness.

Evaporation and sliding behaviors of water droplets were investigated on smooth and rough fluoroalkylsilane coatings. The rough coating possesses nanoscale roughness and chemical heterogeneity on its surface. Evaporation behaviors for these two coatings differed when nanoliter-scale droplets were used, although they were nearly identical for microliter-scale droplets. The droplets on the smooth coating exhibit greater sliding acceleration and a larger slipping velocity ratio than those on the rough coating. Both the evaporation behavior of nanoliter-scale droplets and sliding velocity of microliter-scale droplets were affected by nanoscale surface heterogeneity. They are indicators for highly homogeneous smooth silane coatings.

Effect of surface structure on the sustainability of an air layer on superhydrophobic coatings in a water-ethanol mixture.

Using a laser beam and its reflection, we evaluated surface air layers on two superhydrophobic coatings with different roughnesses (Ra = 1900 and 74 nm) in a water-ethanol mixture. The reflected laser intensity decreased by increasing the ethanol concentration for the superhydrophobic coating with large roughness because of increased scattering by the surface structure of the solid. However, it was almost constant and slightly increased for the coating with small roughness, probably because the liquid-air interface becomes flatter as the liquid intrudes into the surface structure. Results demonstrated that the difference in surface structure provides different sustainability of the surface air layer.

Hydrophobicity and freezing of a water droplet on fluoroalkylsilane coatings with different roughnesses.

Smooth (Ra approximately 0.1 nm) and rough (Ra approximately 20 nm) coatings of 1H,1H,2H,2H-perfluorodecyltrimethoxysilane (FAS-17) were prepared by controlling process conditions. The water contact angles for the smooth and rough coatings were similar (107 degrees and 110 degrees, respectively), but their sliding angles differed considerably (10 degrees and 27 degrees, respectively). The surface potential on the smooth coating, assessed using Kelvin force microscopy, showed a sharp distribution, but that on the rough coating ranged widely, implying large chemical heterogeneity including residual SiOH groups. The freezing temperature of a supercooled water droplet on the rough coating was higher than that on the smooth coating.

Image analysis system for evaluating sliding behavior of a liquid droplet on a hydrophobic surface.

An analysis system was developed to evaluate the sliding behavior of a liquid droplet on a hydrophobic surface. This system enables continuous and simultaneous measurement of both the sliding acceleration and shape deformation during the sliding of a liquid droplet. Moreover, the velocity vector of the internal fluidity of a sliding droplet was obtained by employing particle image velocimetry in the analysis system. This evaluation method pioneers the measurement of the dynamic wettability of a hydrophobic solid surface.

Direct observation of internal fluidity in a water droplet during sliding on hydrophobic surfaces.

In the current study, we used a high-speed camera system with particle image velocimetry to observe the internal fluidity of water droplets during sliding. The droplets' velocity during sliding was controlled by slipping and rolling motions. On the superhydrophobic surface, with a contact angle of 150 degrees, the droplet fell at high velocity by slipping. However, on a normal hydrophobic surface whose water contact angle was around 100 degrees, both slipping and rolling controlled the droplet's velocity during sliding. In addition, the advancing velocity might be large when the slip velocity is large and the contact area is small.