Designing Bioinspired Anti-Biofouling Surfaces based on a Superwettability Strategy.

Anti-biofouling surfaces are of high importance owing to their crucial roles in biosensors, biomedical devices, food processing, the marine industry, etc. However, traditional anti-biofouling surfaces based on either the release of biocidal compounds or surface chemical/physical design cannot satisfy the practical demands when meeting real-world complex conditions. The outstanding performances of natural anti-biofouling surfaces motivate the development of new bioinspired anti-biofouling surfaces. Herein, a novel strategy is proposed for rationally designing bioinspired anti-biofouling surfaces based on superwettability. By utilizing the trapped air cushions or liquid layers, Lotus leaf inspired superhydrophobic surfaces, fish scales inspired underwater superoleophobic surfaces, and Nepenthes pitcher plants inspired omniphobic slippery surfaces have been successfully designed as anti-biofouling surfaces to effectively resist proteins, bacteria, cells, and marine organisms. It is believed that these novel superwettability-based anti-biofouling surfaces will bring a new era to both biomedical technology and the marine industry, and will greatly benefit human health and daily life in the near future.

Controlled self-cleaning aluminum surfaces mediated by anodic aluminum oxide.

Special porous anodic aluminum oxide (AAO) membranes are created on Al in a phosphonic acid electrolyte solution through one-step anodic oxidation and modified with polydimethysiloxane using a vapor deposition technique. In this context, the anodic oxidation time is tuned during its process. As such, the Al surface's wettability, and self-cleaning property are controlled by the tunable anodic oxidation time, for the anodic oxidation, time can regulate the structure of the AAO and the proportion of the air-liquid interface.

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.

Chiral expression from molecular to macroscopic level via pH modulation in terbium coordination polymers.

Chiral expression from the molecular to macroscopic level is common in biological systems, but is difficult to realise for coordination polymers (CPs). The assembly of homochiral CPs in both crystalline and helical forms can provide a bridge for understanding the relationship between the molecular and macroscopic scales of chirality. Herein, we report homochiral helices of [Tb(R- or S-pempH)3]∙2H2O (R - or S -1) (pempH2 = (1-phenylethylamino)methylphosphonic acid) and their crystalline counterparts (R - or S -3), which are formed at different pH of the reaction mixtures under hydrothermal conditions. By combining the experiments and molecular simulations, we propose that the formation of helices of R -1 or S -1 occurs via a hierarchical self-assembly route, which involves twisted packing due to the geometric incompatibility of the different types of chains. The observed chiral transcription from molecules to morphologies is significant for understanding bio-related self-assembly processes on the nano- to macro-scale.

Porous copper surfaces with improved superhydrophobicity under oil and their application in oil separation and capture from water.

The repeatable wettability of the facile-to-fabricate porous copper surface shows superhydrophobicity in air and improved superhydrophobicity under oil. The resultant 3D copper foam can separate and capture oils from water with high separation efficiency, fast capture kinetics, fine mechanical resistance to water impact, and good recyclability.