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A novel porous 3D-structured carbon composite material with a unique architecture by combining graphene and carbonized metal-organic framework (C-MOF) (HKUST-1) microrods for high performing supercapacitors has been synthesised and characterised. The HKUST-1 microrods were prepared by a new method, converting their diamond-like shape into microrods via mechanical shear mixing in an aqueous solution. Grinding of HKUST-1 and graphene oxide (GO) resulted in the formation of a 3D GO-MOF composite with intercalated HKUST-1 microrods between GO sheets. The composite film was treated by a laser scribing method and created a highly porous, a high surface area (>600 m²/g) and conductive 3D nanostructured composite film (L-rGO-C-MOF) used as electrodes for supercapacitor applications. The prepared film showed a high capacitance of 390 F/g at 5 mV/s, and a cyclic stability of 97.8% at 10 A/g after 5000 cycles. The symmetrical supercapacitor delivered an excellent power density of 8037.5 W/kg with an outstanding energy density of 22.3 Wh/kg confirming a new pathway to design new 3D porous graphene-MOF composites for high-performance energy storage devices. Refereed/Peer-reviewed

In comparison with inorganic and dry polymeric materials, conductive polymer hydrogels are promising soft electrode materials due to their unique solid-liquid interface. Nevertheless, the existing hydrogels lack either excellent electrochemical performance or mechanical resilience. Here we report a strategy to overcome this limitation by integrating two types of conducting polymers – polyaniline and PEDOT – through a molecular bridge provided by phytic acid. The acid replaces some of PSS, promoting transformation of PEDOT chains from the benzoic structure to the quinoid structure. The resulting hydrogel consists of a 3D network of PEDOT sheets where PANi are inlaid; it has highly improved mechanical properties in comparison with PEDOT hydrogel due to molecular interactions between PANi and PEDOT. A flexible solid-state supercapacitor based on PEDOT/PANi hydrogel delivered a high volumetric energy density of 0.25 mWh cm−3 at a power density of 107.14 mW cm−3, surpassing many of previously reported solid-state supercapacitors based on PEDOT and hydrogels of other conducting polymers and graphene oxide. This study represents a new direction for the development of conductive polymer composite hydrogels which combine excellent electrochemical performance with mechanical resilience Refereed/Peer-reviewed

Nanoporous alumina (NPA) arrays prepared by electrochemical anodization have been attractive platform for application in molecular separations, biosensing, drug delivery and fuel cells due to their highly ordered pore structures, controllable pore dimensions and unique physical, optical, transport and electrochemical properties. However, there is still a lack of knowledge about the influence of the pore dimensions, shape and surface area on these properties. Hence the aim of this work is to use a focused ion beam (FIB) to mill a barrier layer of NPA to open a either single nanopore, several nanopores and 1 μm and 20 μm square areas of nanopore arrays to explore their electrochemical properties and biosensing performances. The internal surface of opened NPA nanopores was modified by covalent attachment of streptavidin and used for impedance label-free biosensing. The biosensor performance of this antibody modified nanopore biosensing platform was evaluated using various concentrations of biotin as a model analyte. Electrochemical impedance spectrometric (EIS) measurements of pore resistivity were carried out for different patterns of nanopore arrays. The results showed that small areas or number of pores provide better biosensing performance compared to large nanopore arrays. Refereed/Peer-reviewed

Transition metal hexacyanoferrate (MeHCF) have attracted extensive attention because of their outstanding properties including, electrocatalysis, molecular magnetism, biosensing and ion-exchange. This paper describes an approach for fabrication of ordered nanoarrays of Ni hexacyanoferrate (NiHCF) structures with different morphologies such as dots, rods and tubes in order to advance their properties and applications. The method is based on the conversion of Ni into NiHCF nanostructures by electrochemical oxidation in the presence of hexacyanoferrate ions, using nanoporous anodic alumina oxide (AAO) as a template. The structure and morphology of formed Ni and NiHCF nanoarrays were confirmed by scanning electron microscopy (SEM), showing agreement with the pore structures of the AAO template. The electrocatalytic activity of NiHCF nanorod array electrodes showed high catalytic properties for the detection of hydrogen peroxide and the potential to be used as a platform for direct biosensing applications. The ion-exchange ability of fabricated NiHCF nanostructures (nanorods and nanotubes) toward alkali cations such as Na + has been successfully confirmed.