Layer-by-layer assembly of polyelectrolytes on hydrophobic particles in aqueous milieu for efficient dye removal.

Layer-by-layer assembly of strong polyelectrolytes was successfully implemented on hydrophobic particles in degassed saline water thanks to de-gassing-reduced hydrophobic interactions and salinity-reduced hydration. The resulting polyelectrolyte multilayer coated particles were readily converted to hydrophobic yolk/hydrophilic shell particles for the removal of organic dyes from water via both electrostatic and hydrophobic interactions.

Controlled Iodine Phase Transfer of Covalent Organic Framework Membranes for Instant but Sustained Disinfection.

Freestanding membranes of CuCl2-implanted TpPa covalent organic frameworks (COFs) were mechanochemically produced. The resulting membrane had a high I2 adsorption capacity (566.78 g·mol-1) in cyclohexane, which corresponds to 2.2I2 per unit cell with 1.3I2 immobilized on 3Cl- ions (60%) and 0.9 on 3N atoms (40%). Upon being placed in aqueous media, the membrane released 61.1% of its loaded I2 mainly by its Cl- ions within 10 min and the remaining 38.9% mainly from its N atoms within about 5 h. Thanks to that, the COF membranes loaded with 1.5 mg of I2 could be repetitively utilized to kill about 108 CFU/mL E. coli in 0.5-3 min at least five times, after which the membranes could retain their bactericidal activity for 4 h against 108 CFU/mL E. coli. This highlights the promising application of I2-loaded TpPa-CuCl2 COF membranes for instant and sustained disinfection.

Bioinspired, Nanostructure-Amplified, Subcutaneous Light Harvesting to Power Implantable Biomedical Electronics.

Implantable biomedical electronics hold immense promise for in vivo personalized healthy monitoring and even precise therapeutic intervention. Tremendous miniaturization of indwelling modules enables implanted biomedical devices to perform multiple functions with ultralow power consumption but exacerbates the technical challenges of supplying effective power to the devices in vivo. In this Perspective, we summarize new developments in transmitting near-infrared light from sunlight or a light-emitting diode into subcutaneously implanted photovoltaic cells, in which the light utilization efficiency can be amplified with the aid of nanostructured rear reflectors. Considering the many natural examples of nanostructure-induced structural coloration displayed by submarine animals, we wish to open up new prospects of bioinspired, nanostructure-amplified, subcutaneous light harvesting to power implanted biomedical electronics.

Hydrogel-assisted delivery of lipophilic molecules into aqueous medium for transdermal medication based on environment-specific, regioselective adsorption of graphene oxides.

Graphene oxide (GO)-laden agarose composite hydrogels (GOACHs) were utilized to deliver lipophilic molecules from organic to aqueous media without alteration of the lipophilic nature of the molecules and the hydrophilic nature of the GOACHs. After the agarose host networks of the GOACHs were impregnated with the non-polar organic solution of lipophilic molecules via stepwise solvent exchange, their GO guests wielded the edge polar groups to effectively adsorb the lipophilic molecules via hydrogen bonding. After being transferred to aqueous media, the GOACHs were able to not only release the loaded lipophilic molecules but also to adsorb the released lipophilic molecules on the GO non-polar carbon lattice planes via hydrophobic interactions, thus resulting in deliberately balanced release of lipophilic molecules in aqueous media. Based on this environment-specific, regioselective adsorption of their GO guests, the GOACHs were harnessed as carriers for sustained delivery of ibuprofen across rat skin, underpinning their applicability in transdermal medication.

Using Hydrogel to Diversify the Adaptability and Applicability of Functional Nanoparticles: From Nanotech-Flavored Jellies to Artificial Enzymes.

The use of hydrogel to accommodate nanoparticles is generally aimed at a synergetic integration of the peculiar electronic, photonic, magnetic, mechanical, and chemical properties of the nanoparticles with the stimuli-response of the hydrogels into unprecedented, smart, collective functions. The intrinsic water-borne nature of hydrogels further endorses the significant implications of such nanocomposites in biology and medicine. This article will be an account with a special accent on how to introduce nanoparticles within hydrogels and utilize the hydrogels to assist the nanoparticles to adapt themselves into different environments, with a large span of polarity ranging from orthodox aqueous media to unorthodox organic ones. The related technological developments and the associated fundamental issues will be discussed under the umbrella of enabling nanoparticle/hydrogel composites to emulate the unique catalytic performances of enzymes.

Hydrophobic-Force-Driven Removal of Organic Compounds from Water by Reduced Graphene Oxides Generated in Agarose Hydrogels.

Hydrophobic reduced graphene oxides (rGOs) were generated in agarose hydrogel beads (AgarBs) by NaBH4 reduction of graphene oxides (GOs) initially loaded in the AgarBs. The resulting rGO-loaded AgarBs were able to effectively adsorb organic compounds in water as a result of the attractive hydrophobic force between the rGOs in the AgarBs and the organic compounds dissolved in aqueous media. The adsorption capacity of the rGOs was fairly high even toward reasonably water-soluble organic compounds such as rhodamine B (321.7 mg g-1 ) and aspirin (196.4 mg g-1 ). Yet they exhibited salinity-enhanced adsorption capacity and preferential adsorption of organic compounds with lower solubility in water. Such peculiar adsorption behavior highlights the exciting possibility for adopting an adsorption strategy, driven by hydrophobic forces, in practical wastewater treatment processes.

Van der Waals Emulsions: Emulsions Stabilized by Surface-Inactive, Hydrophilic Particles via van der Waals Attraction.

Surface-inactive, highly hydrophilic particles are utilized to effectively and reversibly stabilize oil-in-water emulsions. This is a result of attractive van der Waals forces between particles and oil droplets in water, which are sufficient to trap the particles in close proximity to oil-water interfaces when repulsive forces between particles and oil droplets are suppressed. The emulsifying efficiency of the highly hydrophilic particles is determined by van der Waals attraction between particle monolayer shells and oil droplets enclosed therein and is inversely proportional to the particle size, while their stabilizing efficiency is determined by van der Waals attraction between single particles and oil droplets, which is proportional to the particle size. This differentiation in mechanism between emulsification and stabilization will significantly advance our knowledge of emulsions, thus enabling better control and design of emulsion-based technologies in practice.

Hydrogel-Assisted Transfer of Graphene Oxides into Nonpolar Organic Media for Oil Decontamination.

In this work, graphene oxide (GO)-loaded agarose hydrogel was transferred into oil such as hexadecane via stepwise solvent exchange with no chemical modification of the GO hydrophilic surface and the agarose network. After transfer, the GOs, loaded in the agarose network, could effectively and efficiently adsorb lipophilic dyes in oil via hydrogen bonding between the polar groups of the GOs and the dyes. The maximum adsorption capacity was 355.9 mg g(-1) for Nile red for instance, which is substantially larger than that of pristine agarose hydrogel and hydrophilic GO powder. The dye concentration for effective adsorption can be as low as 0.5 ppm. Thus, the present work demonstrates the promising potential of using hydrophilic adsorbents for efficient removal of polar impurities from oil.