Electrochemical fabrication of graphene nanomesh via colloidal templating.

A simple electrochemical fabrication of graphene nanomesh (GNM) via colloidal templating is reported for the first time. The process involves the arraying of polystyrene (PS) spheres onto a CVD-deposited graphene, electro-deposition of carbazole units, removal of the PS template and electrochemical oxidative etching. The GNM was characterized by scanning electron microscopy (SEM), atomic force microscopy (AFM) and Raman spectroscopy.

On the antibacterial mechanism of graphene oxide (GO) Langmuir-Blodgett films.

The Langmuir-Blodgett (LB) technique was used to immobilize flat graphene oxide (GO) sheets on a PET substrate to ascertain as to whether the edges of GO play an integral part in its antimicrobial mechanism. The observed antibacterial activity suggests that contact with the edges is not a fundamental part of the mechanism.

Design and synthesis of photoresponsive poly(benzyl ester) dendrimers with all-azobenzene repeating units.

A novel class of dendrons and dendrimers containing all-azobenzene units (up to 29 azobenzene groups) was designed and synthesized by the convergent method using a protected orthogonal AB(2) monomer (10) and tetra-functionalized core (11) as building blocks. The preparation of the key monomer (10) involved condensation of a protected nitroso compound (9) and 5-aminoisophthalic acid. These are the first examples of photoresponsive dendrimers with all-azobenzene repeating units. [structure: see text]

On the pH-responsive, charge-selective, polymer-brush-mediated transport probed by traditional and scanning fluorescence correlation spectroscopy.

The complete and reversible charge-selective sequestration of fluorophores by a weak polyelectrolyte brush, poly(2-(dimethylamino)ethylmethacrylate) (PDMAEMA) was demonstrated using fluorescence correlation spectroscopy (FCS). The chemistry and thickness of the weak polyelectrolyte PDMAEMA was tuned reversibly between neutral and cationic polymer forms. Thus, by switching the pH successively, the brush architecture was tuned to selectively trap and release anionic dye probes while continuously excluding cationic molecules. In addition, line-scan FCS was implemented and applied for the first time to a synthetic polymer system and used to identify a new, slower diffusion time on the order of seconds for the sequestered anionic probe under acidic conditions. These results, which quantify the selective sequestration properties of the PDMAEMA brush, are important because they enable a better understanding of transport in polymers and establish a spectroscopic means of evaluating materials with proposed applications in separations science, charge storage/release, and environmental remediation.