To contribute to solving global energy problems, a multifunctional CoFe₂O₄ spinel was synthesized and used as a catalyst for overall water splitting and as an electrode material for supercapacitors. The ultra-fast one-step electrodeposition of CoFe₂O₄ over conducting substrates provides an economic pathway to high-performance energy devices. Electrodeposited CoFe₂O₄ on Ni-foam showed a low overpotential of 270 mV and a Tafel slope of 31 mV/dec. The results indicated a higher conductivity for electrodeposited compared with dip-coated CoFe₂O₄ with enhanced device performance. Moreover, bending and chronoamperometry studies suggest excellent durability of the catalytic electrode for long-term use. The energy storage behavior of CoFe₂O₄ showed high specific capacitance of 768 F/g at a current density of 0.5 A/g and maintained about 80% retention after 10,000 cycles. These results demonstrate the competitiveness and multifunctional applicability of the CoFe₂O₄ spinel to be used for energy generation and storage devices.

Nanotubes made of boron nitride (BN) and carbon have attracted considerable attention within the literature due to their unique mechanical, electrical and thermal properties. In this work, BN and carbon nanotubes, exhibiting high purity (>99%) and similar surface areas (~200 m²/g), were systematically investigated for their thermal stability and oxidation behavior by combining thermal gravimetric analysis and differential scanning calorimetry methods at temperatures of up to ~1300 °C under a synthetic air flow environment. The BN nanotubes showed a good resistance to oxidation up to ~900 °C and fully transformed to boron oxide up to ~1100 °C, while the carbon nanotubes were stable up to ~450 °C and almost completely combusted up to ~800 °C. The different oxidation mechanisms are attributed to the different chemical nature of the two types of nanotubes.

This paper reports a study involving the formation of a self-assembled polymeric monolayer on the surface of a high surface area activated carbon to engineer its affinity towards organic contaminants. A nanoporous activated carbon cloth with a surface area of ∼1220 m² g⁻¹ and a pore volume of ∼0.42 cm³ g⁻¹ was produced by chemical impregnation, carbonisation and high-temperature CO₂ activation of a commercially available viscose rayon cloth. The subsequent modification with a silane polymer resulted in a nanoscale self-assembled monolayer that made it selective towards organic solvents (contact angle 145°). The adsorbent showed more than 95% efficiency in the separation of various types of oil/water mixtures under neutral, basic and acidic conditions. Benefiting from inherent nanoscale features, a robust hierarchical structure and a thermally stable monolayer (∼300 °C), this nanoporous adsorbent maintained high efficiency for more than 20 cycles and separated surfactant stabilised emulsion with >92% oil removal efficiency. The adsorbent was studied extensively with a series of advanced characterisation techniques to establish the formation mechanism and performance in emulsion separation. Findings from this work provide crucial insights towards large-scale implementation of surface engineered activated carbon-based materials for a wide range of industrial separation applications.