Electrochemical removal of anodic aluminium oxide templates for the production of phase-pure cuprous oxide nanorods for antimicrobial surfaces.

Antimicrobial surfaces are ones that incapacitate or kill pathogens landing on them, which could allow for self-sanitising surfaces for hospitals or implants, ensuring healthier stays and procedures. Cuprous compounds such as Cu2O are especially effective at incapacitating both viruses and bacteria, and nanorod arrays have been shown to prevent the adhesion of pathogens and mechanically deform bacteria to the point that their cell walls rupture. A Cu2O nanorod array should therefore allow for the exploitation of both of these effects. In the present work, an electrochemical method is introduced, where Cu2O nanorods formed in a substrate-supported anodic aluminium oxide (AAO) template are held at a stable electrochemical potential throughout the removal of the AAO template. This avoids the partial reduction of the nanorods from Cu2O to Cu that was observed during chemical removal of the template, which was attributed to the presence of residual aluminium from the template fabrication process that reacts with the etchant and lowers the electrochemical potential of the nanorods to a value that favours reduction. Using the electrochemical removal method, the reliable production of phase-pure, free-standing, crystalline Cu2O nanorod arrays on ITO/glass substrates is demonstrated. This simple method is compatible with nanorod arrays of any size.

Clustering effects on discontinuous gold film NanoCells.

Reproducible negative differential resistance (NDR)-like switching behavior is observed in NanoCells. This behavior is attributed to the formation of filaments and clusters between the discontinuous gold films. Control experiments are performed by self-assembly of insulating molecules between the gold islands and conducting molecules on these islands. Additional control experiments are performed by removing the filaments and clusters between islands using a piranha bath. The results are consistent with theoretical predictions and extend the domain of molecular electronics based in organic molecules to include nanosized clusters as active units. This facilitates a scenario where synthetically accessible organic molecules, with defined characteristics, can be adjusted by metallic nanoclusters as an in situ fine-tuning element, able to compensate for the lack of addressing in the nanosize regime.