Reversibly Thermosecreting Organogels with Switchable Lubrication and Anti-Icing Performance.

Synthetic gels with switchable interfacial properties have great potential in smart devices and controllable transport. Herein, we design an organogel by incorporating a binary liquid mixture with an upper critical solution temperature (UCST) into a polymer network, resulting in reversible modulation of lubrication and adhesion properties. As the temperature changes, the lubricating mechanism changes reversibly from boundary lubrication to hydrodynamic lubrication due to phase separation within the binary solution permeating the gel (friction coefficient 0.4-0.03). Droplets appear on the gel surface at low temperature and disappear with temperature higher than the critical phase separation temperature (Tps ) of the organogel. The organogel possesses a relatively low ice adhesive strength (less than 1 kPa). This material has potential applications in anti-icing and smart devices, and we believe that this design strategy can be expanded to other systems such as aqueous solutions and hydrogels.

General Strategy to Fabricate Highly Filled Microcomposite Hydrogels with High Mechanical Strength and Stiffness.

Conventional synthetic hydrogels are intrinsically soft and brittle, which severely limits the scope of their applications. A variety of approaches have been proposed to improve the mechanical strength of hydrogels. However, a facile and ubiquitous strategy to prepare hydrogels with high mechanical strength and stiffness is still a challenge. Here, we report a general strategy to prepare highly filled microcomposite hydrogels with high mechanical performance using an ultrasonic assisted strategy. The microparticles were dispersed in the polymer network evenly, resulting in homogeneous and closely packed structures. The as-prepared hydrogels with extraordinary mechanical performance can endure compressive stress up to 20 MPa (at 75% strain) and exhibit high stiffness (elastic modulus is around 18 MPa). By using our comprehensive strategy, different hydrogels can enhance their mechanical strength and stiffness by doping various microparticles, leading to a much wider variety of applications.

Covalent tethering of photo-responsive superficial layers on hydrogel surfaces for photo-controlled release.

The diffusion and transport of substances between a hydrogel and its environment have received tremendous research interest, due to the wide range of applications of hydrogel materials in fields related to drug carriers and drug delivery vehicles. To date, much research has been done to tailor the diffusion and transport of substances through hydrogels, where most efforts were focused on tuning the 3D network properties of the hydrogel including loop size, hydrophobicity of building blocks and the stimuli-responsive properties of backbones. These conventional strategies, however, usually suffer from complicated fabrication procedures and result in a homogeneous increase in hydrophobicity of the hydrogel network, leading to low efficiency control over the diffusion of substances through the hydrogel. Herein, a facile strategy that can functionalize the surfaces of hydrogels, while keeping the interior network unchanged, was reported, and is realized by quaternization reaction confined to the hydrogel/oil interface. Owing to the introduction of the photo-responsive molecule IBSP as a modifier, the surface wettability of the resulting hydrogel can be controlled by light both in air and underwater environments. Consequently, the diffusion rate of a substance through this modified hydrogel can be regulated by light, which brings convenience to the controlled release of hydrogels and other hydrogel-related fields.

Interfacial Engineering of Hierarchically Porous NiTi/Hydrogels Nanocomposites with Exceptional Antibiofouling Surfaces.

Seamlessly bridging the hard and the soft, a strategy to fabricate hierarchically porous NiTi/hydrogels nanocomposites is reported. The nanocomposite surface can hold high-content water while keeping its hierarchical nanoscale topography, thus showing exceptional antibiofouling performance. This strategy will lead to antibiofouling alloy (e.g., NiTi)/hydrogel nanocomposites for improved stents and other blood-contacting implants and medical devices.

Controllable Fabrication of Noniridescent Microshaped Photonic Crystal Assemblies by Dynamic Three-Phase Contact Line Behaviors on Superhydrophobic Substrates.

Enormous research efforts have been made to self-assemble monodisperse colloidal spheres into special microscopic shapes (e.g., superbeads, superballs, or doughnuts), due to their widespread applications in sensors, displays, separation processes, catalysis, etc. But realization of photonic crystal (PC) assemblies with both facile microshape control and a noniridescent property is still a tough task. Herein, we demonstrate the controllable fabrication of noniridescent microshaped PC assemblies by evaporation-induced self-assembly inside aqueous colloidal dispersion droplet templates on superhydrophobic substrates. The microshapes of the PC assemblies could be tuned from microbeads to microwells to microellipsoids by manipulating the dynamic behaviors of the three-phase contact line of the colloidal droplets during the evaporating process. Structure characterization shows that the PC assemblies are crack-free, consisting of an ordered periodic arrangement of colloidal spheres in the surface layers and amorphous inner layers. The incorporation of black Fe3O4 nanoparticles into the PC assembly lattice is demonstrated to endow the PC assemblies with enhanced noniridescent structural colors with wide-viewing angles and a superparamagnetic property. The crack-free noniridescent PC assemblies with controlled microshapes have promising applications in the fields of nontoxic, nonbleaching pigments and energy-efficient full-color display pixels, and their facile fabrication procedure may provide guidance for creating new types of substructured colloidal particles.

Self-Replenishable Anti-Waxing Organogel Materials.

Solid deposition, such as the formation of ice on outdoor facilities, the deposition of scale in water reservoirs, the sedimentation of fat, oil, and grease (FOG) in sewer systems, and the precipitation of wax in petroleum pipelines, cause a serious waste of resources and irreversible environmental pollution. Inspired by fish and pitcher plants, we present a self-replenishable organogel material which shows ultra-low adhesion to solidified paraffin wax and crude oil by absorption of low-molar-mass oil from its crude-oil environment. Adhesion of wax on the organogel surface was over 500 times lower than adhesion to conventional material surfaces and the wax was found to slide off under the force of gravity. This design concept of a gel with decreased adhesion to wax and oil can be extended to deal with other solid deposition problems.