Single-layer graphene is interesting as a flexible 2D material, with xy-dimensions variable up to a centimetre in length and a z-thickness of a single carbon atom. It conducts heat and electricity, has excellent mechanical strength, and is impermeable to gases except hydrogen gas. Its drawback: how to disperse it in a liquid. When you try to do this flexible sheets of graphene tend to stack as a result of attractive van der Waals interactions, making it virtually an impossible material to disperse as single sheets.
As a compromise, people came up with graphene oxide (GO), it’s oxidised analogue. The presence of oxygen atoms containing functional groups, such as hydroxy, epoxy, carboxylic acid, ketone, or aldehyde, provides it with a polarity, which makes it possible to disperse GO as single sheets in polar solvents, such as water or DMSO at low concentrations in the absence of electrolyte or other colloidal particles. The drawbacks: graphene oxide sheets have holes. Whereas graphene can be seen as a pristine, flexible bedsheet, graphene oxide is a bedsheet attacked by moths. This makes the material less suitable for barrier property reinforcement. Graphene oxide is also less electrically conducting as oxidation has partially destroyed its conjugation. Nevertheless, it still shows great potential for a range of applications, for example, those that need mechanical reinforcement, such as polymer nano-composites, but only if we can enhance its dispersibility in liquids or polymer melts.
Grafting polymer chains from the surface of GO allows it to be dispersed more easily. This can provide additional electrostatic and steric stabilization against sheet stacking at higher concentrations in less polar solvents or contain soluble polymer chains or non-interacting particles that can trigger depletion flocculation.
There are several approaches to accomplishing this, each with advantages and disadvantages. A particular challenge is linking a sufficient mass of polymer chains to the GO’s surface. In our gold open access paper recently published in the RSC journal Polymer Chemistry, we report a way to address this, employing radical polymerization reactions that lead to a branched polymer architecture. Methacrylate-based macromonomers made by catalytic chain transfer polymerization were used together as molecular weight regulators with dimethacrylates as crosslinkers to introduce branching points.
You can read the paper here: