Liquid-Assisted Single-Layer Janus Membrane for Efficient Unidirectional Liquid Penetration.

Unidirectional liquid penetration plays an important role in many fields, such as microfluidic devices, biological medical, liquid printing, and oil/water separation. Although there are some progresses in the liquid unidirectional penetration using a variety of Janus membranes with anisotropic wettability, it still remains a great difficulty for single-layer Janus membranes with straight pore to balance spontaneous liquid penetration in positive direction and superior liquid resistance in the reverse direction. Herein, a liquid-assisted strategy for single-layer Janus membrane is developed, which can efficiently decrease the critical breakthrough pressure from superhydrophobic side to hydrophilic side and show little influence on that in the reverse direction. Consequently, unidirectional water penetration with high hydraulic pressure difference can be achieved. The Laplace pressure change along the thickness of the single-layer Janus membranes is further discussed, and the mechanism by which the auxiliary liquid decreases the critical breakthrough pressure is revealed. Furthermore, this Janus membrane with unidirectional water penetration "diode" performance can be used to prevent liquid backflow in intravenous transfusion. It is believed that this work can open an avenue for people to design single-layer Janus membrane with high pressure difference and find wide applications in unidirectional liquid transport.

Molecular-Structure-Induced Under-Liquid Dual Superlyophobic Surfaces.

Surfaces with under-water superoleophobicity or under-oil superhydrophobicity have attractive features due to their widespread applications. However, it is difficult to achieve under-liquid dual superlyophobic surfaces, that is, under-oil superhydrophobicity and under-water superoleophobicity coexistence, due to the thermodynamic contradiction. Herein, we report an approach to obtain the under-liquid dual superlyophobic surface through conformational transitions of surface self-assembled molecules. Preferential exposure of either hydrophobic or hydrophilic moieties of the hydroxythiol (HS(CH2)nOH, where n is the number of methylene groups) self-assembled monolayers to the surrounding solvent (water or oil) can be used to manipulate macroscopic wettability. In water, the surfaces modified with different hydroxythiols exhibit under-water superoleophobicity because of the exposure of hydroxyl groups. In contrast, surface wettability to water is affected by molecular orientation in oil, and the surface transits from under-oil superhydrophilicity to superhydrophobicity when n ≥ 4. This surface design can amplify the molecular-level conformational transition to the change of macroscopic surface wettability. Furthermore, on-demand oil/water separation relying on the under-liquid dual superlyophobicity is successfully demonstrated. This work may be useful in developing the materials with opposite superwettability.

Multifunctional Magnetocontrollable Superwettable-Microcilia Surface for Directional Droplet Manipulation.

In nature, fluid manipulations are ubiquitous in organisms, and they are crucial for many of their vital activities. Therefore, this process has also attracted widescale research attention. However, despite significant advances in fluid transportation research over the past few decades, it is still hugely challenging to achieve efficient and nondestructive droplet transportation owing to contamination effects and controllability problems in liquid transportation applications. To this end, inspired by the motile microcilia of micro-organisms, the superhydrophobicity of lotus leaves, the underwater superoleophobicity of filefish skin, and pigeons' migration behavior, a novel manipulation strategy is developed for droplets motion. Specifically, herein, a superwettable magnetic microcilia array surface with a structure that is switchable by an external magnetic field is constructed for droplet manipulation. It is found that under external magnetic fields, the superhydrophobic magnetic microcilia array surface can continuously and directionally manipulate the water droplets in air and that the underwater superoleophobic magnetic microcilia array surface can control the oil droplets underwater. This work demonstrates that the nondestructive droplet transportation mechanism can be used for liquid transportation, droplet reactions, and micropipeline transmission, thus opening up an avenue for practical applications of droplet manipulation using intelligent microstructure surfaces.

Surfactant-free exfoliation of multilayer molybdenum disulfide nanosheets in water.

In this study, we report a potentially scalable method for producing multilayer molybdenum disulfide (MoS2) nanosheets. The addition of a small amount of ammonia solution can improve the exfoliation of MoS2 nanosheets in water. The surface charge induced by spontaneous adsorption of hydroxyl ions on MoS2 surfaces favors the exfoliation process. The edge charge generated by the ionization of edge-attached groups facilities the dispersion of exfoliated nanosheets in water. It is also found that smaller MoS2 nanosheets show an improved photocatalytic performance, which stems from enhanced edge effects and a reduced flake thickness. This work opens a new vista on preparation and application of multilayer MoS2 nanosheets.

Understanding the exfoliation and dispersion of MoS2 nanosheets in pure water.

Exfoliation and dispersion of two dimensional (2D) transition metal dichacogenides (TMDCs) such as MoS2 in water are highly demanded. In this paper, we exfoliate MoS2 nanosheets in pure water via ultrasonication and attempt to understand the exfoliation process and the dispersion behavior of hydrophobic MoS2. Cavitation-induced exfoliation leads to thinning and fragmentation of MoS2 flakes. Formation of mesoporous MoS2 sheets suggests that the exfoliation initiates from the basal planes. As for the dispersion of MoS2 nanosheets in water, we find that higher centrifugation rate and thus smaller lateral size, results in improved stability. This can be attributed to the enhanced edge effects. Fragmentation of MoS2 flakes generates many edges, to which hydrophilic and ionizable groups are attached. Herein, the edge effects include two aspects. On the one hand, edge-attached polar and hydrophilic groups promote interactions of MoS2 nanosheets with water molecules and result in better wettability, which can be explained by the hemi-wicking model. On the other hand, dissociation of these groups makes MoS2 sheets negatively charged. It is found that edge charge dominates. As the flake size reduces, attractive van der Waals force and hydrophobic force can be overcome by electrostatic repulsions, which prevent MoS2 nanosheets from aggregation. This study opens a new vista on exfoliating and dispersing hydrophobic 2D nanomaterials in water.

Direct exfoliation of graphite in water with addition of ammonia solution.

To bring graphene closer to its real-world applications, finding a green, low-cost, environment-friendly and less toxic solvent for production of high-quality graphene is highly demanded. However, water, the most widely used green solvent, is generally considered to be a poor solvent for hydrophobic graphene. In this study, we exfoliate graphene nanosheets directly in basic water without surfactants, polymers or organic solvents. The addition of a small amount of ammonia solution achieves the exfoliation of few-layer graphene nanosheets from pristine graphite. Diverse characterization methods are employed to investigate the morphology and quality of as-prepared graphene sheets. The release of gaseous ammonia plays the key role in exfoliation of graphene. The concentration of stable graphene dispersions can reach 0.058mg/mL.