Graphene Oxide Sheets in Solvents: To Crumple or Not To Crumple?

Some earlier studies suggested that graphene oxide (GO) sheets adopt a crumpled configuration in water, similar to the shape of a paper ball, which turns into an even more compact, collapsed form upon addition of a poor solvent due to enhanced intrasheet affinity. Although those results have been debated in studies concerning membrane configurations, they are now often used to justify the existence of folds and wrinkles in solution-processed GO-based structures. This has led to a misconception that wrinkled and crumpled features may be intrinsic to solution processing and unavoidable.

Control of Selective Ion Transfer across Liquid-Liquid Interfaces: A Rectifying Heterojunction Based on Immiscible Electrolytes.

The current rectification displayed by solid-state p-n semiconductor diodes relies on the abundance of electrons and holes near the interface between the p-n junction. In analogy to this electronic device, we propose here the construction of a purely ionic liquid-state electric rectifying heterojunction displaying an excess of monovalent cations and anions near the interface between two immiscible solvents with different dielectric properties. This system does not need any physical membrane or material barrier to show preferential ion transfer but relies on the ionic solvation energy between the two immiscible solvents.

Self-dispersed crumpled graphene balls in oil for friction and wear reduction.

Ultrafine particles are often used as lubricant additives because they are capable of entering tribological contacts to reduce friction and protect surfaces from wear. They tend to be more stable than molecular additives under high thermal and mechanical stresses during rubbing. It is highly desirable for these particles to remain well dispersed in oil without relying on molecular ligands.

Supramolecular Packing Controls H₂ Photocatalysis in Chromophore Amphiphile Hydrogels.

Light harvesting supramolecular assemblies are potentially useful structures as components of solar-to-fuel conversion materials. The development of these functional constructs requires an understanding of optimal packing modes for chromophores. We investigated here assembly in water and the photocatalytic function of perylene monoimide chromophore amphiphiles with different alkyl linker lengths separating their hydrophobic core and the hydrophilic carboxylate headgroup.

Self-assembled two-dimensional nanofluidic proton channels with high thermal stability.

Exfoliated two-dimensional (2D) sheets can readily stack to form flexible, free-standing films with lamellar microstructure. The interlayer spaces in such lamellar films form a percolated network of molecularly sized, 2D nanochannels that could be used to regulate molecular transport. Here we report self-assembled clay-based 2D nanofluidic channels with surface charge-governed proton conductivity.

Self-assembling hydrogel scaffolds for photocatalytic hydrogen production.

Integration into a soft material of all the molecular components necessary to generate storable fuels is an interesting target in supramolecular chemistry. The concept is inspired by the internal structure of photosynthetic organelles, such as plant chloroplasts, which colocalize molecules involved in light absorption, charge transport and catalysis to create chemical bonds using light energy. We report here on the light-driven production of hydrogen inside a hydrogel scaffold built by the supramolecular self-assembly of a perylene monoimide amphiphile.