Nicholas P. Power

Ti₃C₂Tₓ MXene was synthesised via an optimised low-temperature molten salt method using ammonium bifluoride. Complete MAX (Ti3AlC2) phase etching was achieved within 5 minutes at a temperature of 150 °C. Structural and compositional characterisation of Ti₃C₂Tₓ MXene confirmed well-exfoliated Ti3C2Tx sheets with com-plete Al removal. The synthesised Ti₃C₂Tₓ MXene was integrated as the active switch-ing layer in lateral and vertical memristor geometries. Both geometries exhibited non-linear bipolar resistive switching. The vertical device exhibited an on-state current of ~10 mA and stable resistance retention of over 120 minutes. UV-Ozone treatment of lateral devices resulted in the I-V characteristics changing from bipolar to asymmetric with rectifying characteristics. These results establish a broadly accessible, low-cost prototyping framework for Ti₃C₂Tₓ MXene -based memristor devices.

Centrifugal spinning was utilized in producing polyacrylonitrile (PAN) nanofibers loaded with extractant di-(2-ethylhexyl) phosphoric acid (D2EHPA) for efficient adsorption recovery of gallium from aqueous solutions. The adsorption experimental data were best fitted by a pseudo-second-order kinetic model and the BET equilibrium isotherm model. Optimal adsorption performance by the PAN/D2EHPA nanofibers exhibited an adsorption capacity of 33.13 mg g⁻¹ for the recovery of gallium at pH 2.5 and 55 °C. The thermodynamic parameters demonstrated that adsorption was endothermic, spontaneous, and favorable. The stability and reusability of the nanofibers was assessed, demonstrating retention of structural and functional integrity for the nanofibers over five cycles of an adsorption/desorption process, whilst retaining adsorption efficiency. The results demonstrate that PAN/D2EHPA nanofibers have excellent potential for utilization in an efficient adsorption process for gallium recovery, offering significant positive environmental impact over conventional liquid–liquid extraction methods.

A rapid synthesis of TiO₂ hybrids with significant enhancement in photocatalytic activity is reported. Using state-of-the-art techniques including sophisticated DFT calculations, we report insight into the charge transfer and modulation of the energy band edges.

With a worldwide ever increasing demand for metals, particularly for the manufacture of electronics and batteries, there is not only a concurrent need to recover these materials from their subsequent waste streams but also a need to make advancements to do this via development of more efficient and eco-friendly processes for metal recovery; solid-phase extraction can be considered a promising alternative to conventional processes. This work studied the production of novel nanofibers modified with Cyanex 272 and their application in the recovery of cobalt present in aqueous solution The nanofibers produced by forcespinning were characterized by SEM, FT-IR and TGA and the extraction of cobalt was evaluated by variation of the pH, solid:liquid (S:L) ratio, extraction time and Cyanex 272 content in the nanofibers. The best extraction efficiency was 99.96%, achieved under the following conditions: pH 8; (S:L) ratio of 1:200; 25% of Cyanex 272; Extraction time of 60 min. The maximum extraction capacity obtained was 15.46 mg Co/g of nanofiber and 70.15 mg Co/g of extractor. In successive reuse cycles, the results demonstrated that the extraction efficiency was maintained at over 85%. The findings showed that Nylon 6/Cyanex 272 nanofibers are a new robust and promising material for the recovery of heavy metals from aqueous solution, confirming that nanofibers have an efficiency similar to conventional liquid–liquid extraction, without the disadvantage of volatile organic compounds emissions generated by the use of organic diluents. GRAPHICAL ABSTRACT

MXene (Ti ₂ CT _x ) is exfoliated in a vortex fluidic device (VFD), as a thin film microfluidic platform, under continuous flow conditions, down to ca 3 nm thin multi-layered two-dimensional (2D) material, as determined using AFM. The optimized process, under an inert atmosphere of nitrogen to avoid oxidation of the material, was established by systematically exploring the operating parameters of the VFD, along with the concentration of the dispersed starting material and the choice of solvent, which was a 1 : 1 mixture of isopropyl alcohol and water. There is also some fragmentation of the 2D material into nanoparticles ca 68 nm in diameter.

Oxidation of MXene in a vortex fluidic device (VFD) operating under continuous flow results in exfoliation and fragmentation into nanoparticles of surface oxidised 2D material with further oxidation of the nanoparticles into anatase (TiO₂). These MXene and anatase nanoparticles co‐assemble into stable micron sized spheres which are topologically smooth, decorating the surface of exfoliated MXene. The formation of this composite material in the dynamic thin film in the VFD was optimised by systematically exploring the operating parameters of the microfluidic platform, determined at 45° tilt angle for the 20 mm diameter glass tube spinning at 5k rpm, with a flow rate of a colloidal dispersion of MXene in aqueous H₂O₂ (30%) at 0.75 mL/min at a concentration of MXene of 0.5 mg/mL.

Blue-luminescent N-doped carbon quantum dots (NCQDs) exhibiting rarely observed excitation independent optical properties are synthesised from citric acid in the presence of ammonia via a Continuous Hydrothermal Flow Synthesis (CHFS) approach. CHFS is an eco-friendly, rapid synthetic approach (within fractions of a second) facilitating ease of scale-up industrialization as well as offering materials with superior properties. The synthesised NCQDs readily disperse in aqueous solution, have an average particle size of 3.3 ± 0.7 nm, with highest emission intensity at 441 nm (and a narrow full width at half maximum, FWHM ∼78 nm) under a 360 nm excitation wavelength. N-doped carbon quantum dots, without any further modification, exhibited a high selectivity and sensitivity as a nano-sensor for the highly toxic and carcinogenic chromium(VI) ions. The nano-chemo-sensor delivers significant advantages including simplicity of manufacturing via a continuous, cleaner technology (using targeted biomass precursor), high selectivity, sensitivity and fast response leading to potential applications in environmental industry as well photovoltaics, bio-tagging, bio-sensing and beyond.

Green fluorescent graphene quantum dots (GQD) have been synthesized via hydrothermal fragmentation using a continuous hydrothermal flow synthesis (CHFS) process as a single, rapid and environmentally benign method. This is in the presence of p-phosphonic acid calix[4]arene which enhances the optical properties of the graphene quantum dots through surface functionalization, with photoluminescence quantum yields of up to 4.5%. Potential environmental impact of a lab-scale supercritical CHFS process compared with that of conventional batch processing of GQDs has been assessed using the method of the International Reference Life Cycle Data System (ILCD).