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Surfaces with photoswitchable wettability are of great interest for various applications such as smart coatings or liquid condensation. The photochromic ring opening reaction of spiropyran (SP) to merocyanine (MC) implies a high dipole moment change, making it interesting for photo‐controlled wetting properties. In addition to the material chemistry, surface wettability is influenced by the surface topography. Porous SP copolymers with various micro‐/nanostructures, that is, different submicron roughness, are fabricated via polymerization‐induced phase separation. The influence of the surface topography on the photoswitchable wetting properties is studied. Surfaces with arithmetic mean roughness (Sa) below 150 nm exhibited a maximum static contact angle (SCA) photoswitch up to 16° from 124 ± 6° to 108 ± 4° upon UV exposure. While superhydrophobic surfaces with higher Sa (157 – 608 nm) showed an insignificant SCA switch. The latter surfaces have a SCA above 150° and low CA hysteresis indicating small and insufficient contact with SP/MC surface asperities for the switch. With the optimized surfaces, photo‐controlled water condensation is studied on microscale and showed that the condensate droplets merged faster, and formed larger droplets pinned to the original contact lines on surfaces switched to the less hydrophobic state. [ABSTRACT FROM AUTHOR]

Superhydrophobic coatings are widely applicable, e.g., as self‐cleaning surfaces or water–oil separation membranes, yet their wider usage is impeded due to costs of fabrication, size, or substrate limitation. Spray‐coating is a versatile coating procedures and might offer a good solution for the fabrication of these superhydrophobic coatings, due to the fact that coatings can be fabricated on various materials in a simple, fast, and inexpensive manner. Most procedures rely on hybrid coatings of hydrophobized nanoparticles and a polymeric matrix, which have several drawbacks including the easy loss of nanoparticles and difficult waste handling. Here, the fabrication of the superhydrophobic material, called Fluoropor, for the first time, by spray‐coating on various substrates including metals, tissues, concrete, and glass is presented. It is fabricated by spray‐coating a mixture of a highly fluorinated monomer blended with porogens followed by photopolymerization. The superhydrophobicity of the material relies on the porous structure on the micro‐/nanoscale across the bulk material and does not require any nanoparticles. Excellent self‐cleaning ability of these coatings, resistance against thermal and abrasive impact, and their application as oil–water separation membranes are shown. This versatile applicability is highly promising for real‐world application as self‐cleaning coatings or oil–water separating membranes. [ABSTRACT FROM AUTHOR]

The transfer of stretchable electrodes or devices from one substrate to another thin elastomer is challenging as the elastic stamp often yields a huge strain beyond the stretchability limit of the electrodes at the debonded interface. This will not happen if the stamp is rigid. However, a rigid material cannot be used as the substrate for stretchable electrodes. Herein, silk fibroin with tunable rigidity (Young's modulus can be changed from 134 kPa to 1.84 GPa by controlling the relative humidity) is used to transfer highly stretchable metal networks as highly conformable epidermal electrodes. The silk fibroin stamp is tuned to be rigid during peeling, and then be soft and highly stretchable as a substrate when laminated on moisturized human skin. In addition, the epidermal electrodes exhibit no skin irritation or inflammation after attaching for over 10 d. The high compliance results in a lower interface impedance and lower noises of the electrode in measuring electromyographic signals, compared with commercial Ag‐AgCl gel electrodes. The strategy of tuning the rigidity at different stages of transfer is a general method that can be extended to the transfer of other stretchable electrodes and devices for epidermal electronics, human machine interfaces, and soft robotics. [ABSTRACT FROM AUTHOR]

Human–computer interfaces, smart glasses, touch screens, and some electronic skins require highly transparent and flexible pressure‐sensing elements. Flexible pressure sensors often apply a microstructured or porous active material to improve their sensitivity and response speed. However, the microstructures or small pores will result in high haze and low transparency of the device, and thus it is challenging to balance the sensitivity and transparency simultaneously in flexible pressure sensors or electronic skins. Here, for a capacitive‐type sensor that consists of a porous polyvinylidene fluoride (PVDF) film sandwiched between two transparent electrodes, the challenge is addressed by filling the pores with ionic liquid that has the same refractive index with PVDF, and the transmittance of the film dramatically boosts from 0 to 94.8% in the visible range. Apart from optical matching, the ionic liquid also significantly improves the signal intensity as well as the sensitivity due to the formation of an electric double layer at the dielectric‐electrode interfaces, and improves the toughness and stretchability of the active material benefiting from a plasticization effect. Such transparent and flexible sensors will be useful in smart windows, invisible bands, and so forth. [ABSTRACT FROM AUTHOR]

A new kind of agar-polyacrylamide/graphene oxide (agar-PAM/GO) nanocomposite double network (DN) hydrogels is successfully synthesized using one-pot method. The agar-PAM/GO DN hydrogel consists of first agar network cross-linked via hydrogen bond and second PAM network with GO severing as physically cross-linking agent. The factors that influence the mechanical properties of agar-PAM/GO DN gel is investigated. The DN hydrogel exhibits excellent mechanical properties with fracture strain of 4 600% and fracture strength of 332 kPa. In addition, the DN hydrogel shows a good fatigue resistance and self-healing ability. [ABSTRACT FROM AUTHOR]