Inspired by biointerfaces, such as the surfaces of lotus leaves and pitcher plants, researchers have developed innovative strategies for controlling surface wettability and transparency. In particular, great success has been achieved in obtaining low adhesion and high transmittance via the introduction of a liquid layer to form liquid-infused surfaces. Furthermore, smart surfaces that can change their surface properties according to external stimuli have recently attracted substantial interest. As some of the best-performing smart surface materials, slippery liquid-infused porous surfaces (SLIPSs), which are super-repellent, demonstrate the successful achievement of switchable adhesion and tunable transparency that can be controlled by a graded mechanical stimulus. However, despite considerable efforts, producing temperature-responsive, super-repellent surfaces at ambient temperature and pressure remains difficult because of the use of nonreactive lubricant oil as a building block in previously investigated repellent surfaces. Therefore, the present study focused on developing multifunctional materials that dynamically adapt to temperature changes. Here, we demonstrate temperature-activated solidifiable/liquid paraffin-infused porous surfaces (TA-SLIPSs) whose transparency and control of water droplet movement at room temperature can be simultaneously controlled. The solidification of the paraffin changes the surface morphology and the size of the light-transmission inhibitor in the lubricant layer; as a result, the control over the droplet movement and the light transmittance at different temperatures is dependent on the solidifiable/liquid paraffin mixing ratio. Further study of such temperature-responsive, multifunctional systems would be valuable for antifouling applications and the development of surfaces with tunable optical transparency for innovative medical applications, intelligent windows, and other devices.

Liquid‐infused coatings are because of their fluidity of considerable technological importance for hydrophobic materials with multifunctional properties, such as self‐healing, transmittance, and durability. However, conventional coatings absorb viscous liquid into their sponge‐like structured surface, causing uncontrollable liquid layer formation or liquid transport. In addition, a hydrophobic‐liquid‐retained surface can cause instability and lead to limitation of the hydrophobicity, optical properties, and flexibility due to liquid layer evaporation. Here, we report a strategy for controllable liquid‐layer formation on smooth surfaces (R rms < 1 nm) by π ‐electron interactions. Using this technology, superoleophilic wetting of decyltrimethoxysilane results in the design of a surface with π ‐interaction liquid adsorption, smoothness, and hydrophobicity (SPLASH), that shows extraordinary hydrophobicity (CAH = 0.75°), and stable repellence for various water‐based solutions including micrometer‐sized mist. The smoothness of the solid under a liquid layer enabled the SPLASH to exhibit stable hydrophobicity, transparency (>90%), structure damage durability and flexibility, regardless of the liquid layer thickness by bending or evaporation. Furthermore, the patterned π ‐electrons' localization on the smooth coating enables controlled liquid‐layer formation and liquid transport. This strategy may provide new insights into designing functional liquid surfaces and our designed surface with multifunctional properties could be developed for various applications.

In this letter, we introduce a novel liquid manipulation strategy to design dynamically hydrophobic and statically hydrophobic/hydrophilic patterned surfaces using an "omniphobicity"-based technique. The surfaces guide the sliding direction of a droplet in the presence of a statically hydrophilic area where the droplet does not stick on the transport path significantly enhancing the fluidic system transport efficiency. The concept of dynamically hydrophobic and statically hydrophobic/hydrophilic patterned surfaces in conjunction with omniphobic patterning techniques having surface multifunctionality, we believe, has potential not only for fluidic applications but also for future material engineering development.

Control of vapor condensation properties is a promising approach to manage a crucial part of energy infrastructure conditions. Heat transfer by vapor condensation on superhydrophobic coatings has garnered attention, because dropwise condensation on superhydrophobic surfaces with rough structures leads to favorable heat-transfer performance. However, pinned condensed water droplets within the rough structure and a high thermodynamic energy barrier for nucleation of superhydrophobic surfaces limit their heat-transfer increase. Recently, slippery liquid-infused surfaces (SLIPS) have been investigated, because of their high water sliding ability and surface smoothness originating from the liquid layer. However, even on SLIPS, condensed water droplets are eventually pinned to degrade their heat-transfer properties after extended use, because the rough base layer is exposed as infused liquid is lost. Herein, we report a liquid-infused smooth surface named "SPLASH" (surface with π electron interaction liquid adsorption, smoothness, and hydrophobicity) to overcome the problems derived from the rough structures in previous approaches to obtain stable, high heat-transfer performance. The SPLASH displayed a maximum condensation heat-transfer coefficient that was 175% higher than that of an uncoated substrate. The SPLASH also showed higher heat-transfer performance and more stable dropwise condensation than superhydrophobic surfaces and SLIPS from the viewpoints of condensed water droplet mobility and the thermodynamic energy barrier for nucleation. The effects of liquid-infused surface roughness and liquid viscosity on condensation heat transfer were investigated to compare heat-transfer performance. This research will aid industrial applications using vapor condensation.

As frost formation and ice accumulation result in serious problems in various industrial systems, some anti-icing system is highly required, and passive anti-icing processes based on ice prevention coatings have attracted much attention. Recently, antifreeze liquid-infused surfaces (LISs) have been developed for the preparation of ice-phobic surfaces owing to their low ice adhesion strength and antifrosting properties. However, it is still challenging to add an optical function such as high transparency to antifreeze LISs despite the potential for the application in window coatings. In addition, the influence on anti-icing properties by the thickness of antifreeze liquid layer and base layer are still unclear. Here, we designed highly transparent coating surfaces that were resistant to ice adhesion and frost formation. We controlled the thickness, surface roughness, and refractive index of the base layer through a spray layer-by-layer (LbL) method and then investigated the effect on the optical properties, ice adhesion strength, and frost formation behavior. The frost-resisting properties of the surfaces were clearly improved with the increase of the lubricant thickness as well as the increase of the number of bilayers; the parallel transmittance of antifreeze LIS composed of ethylene glycol and this base layer was approximately 92.6%, and the ice adhesion strength was below 17 kPa regardless of the number of bilayers. These results indicated that a high lubricant thickness coating can achieve both excellent anti-icing properties and transparency; the antifreeze LIS based on a 100 bilayer base coating had excellent antifrosting properties owing to its thick antifreeze liquid layer and maintained both of high transparency and low ice adhesion. Furthermore, the spray LbL method makes it possible to fabricate the base layer in short time and also in large scale, which is quite useful for the practical application of antifreeze LIS. This work will be of enormous help for the design of transparent anti-icing coatings as well as industrial applications such as solar cells and the windows of transportation vehicles.