The oxidation of methanol is studied at TiO₂-supported Pt electrodes of varied high surface area carbon content (in the 30-5% w/w range) and C÷Ti atom ratio (in the 3.0-0.4 ratio). The Pt-TiO₂ catalyst is prepared by a photo-deposition process and C nanoparticles (Vulcan XC72R) are added by simple ultrasonic mixing. The optimum C÷Ti atom ratio of the prepared catalyst for methanol electro-oxidation is found to be 1.5, resulting from the interplay of C properties (increased electronic conductivity and methanol adsorption), those of TiO₂ (synergistic effect on Pt and photo-activity), as well as the catalyst film thickness. The intrinsic catalytic activity of the best Pt-TiO₂/C catalyst is better than that of a commercial Pt/C catalyst and could be further improved by nearly 25% upon UV illumination, whose periodic application can also limit current deterioration.

Polymer electrolyte membrane (PEM) water electrolyzers suffer mainly from slow kinetics regarding the oxygen evolution reaction (OER). Noble metal oxides, like IrO₂ and RuO₂, are generally more active for OER than metal electrodes, exhibiting low anodic overpotentials and high catalytic activity. However, issues like electrocatalyst stability under continuous operation and cost minimization through a reduction in the catalyst loading are of great importance to the research community. In this study, unsupported IrO₂ of various particle sizes (different calcination temperatures) were evaluated for the OER and as anode electrodes for PEM water electrolyzers. The electrocatalysts were synthesized by the modified Adams method, and the effect of calcination temperature on the properties of IrO₂ electrocatalysts is investigated. Physicochemical characterization was conducted using X-ray diffraction (XRD), Brunauer–Emmett–Teller (BET) surface area measurement, high-resolution transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS) analyses. For the electrochemical performance of synthesized electrocatalysts in the OER, cyclic voltammetry (CV) and linear sweep voltammetry (LSV) were conducted in a typical three-cell electrode configuration, using glassy carbon as the working electrode, which the synthesized electrocatalysts were cast on in a 0.5 M H₂SO₄ solution. The materials, as anode PEM water electrolysis electrodes, were further evaluated in a typical electrolytic cell using a Nafion^®115 membrane as the electrolyte and Pt/C as the cathode electrocatalyst. The IrO₂ electrocatalyst calcined at 400 °C shows high crystallinity with a 1.24 nm particle size, a high specific surface area (185 m² g⁻¹), and a high activity of 177 mA cm⁻² at 1.8 V for PEM water electrolysis.

Preparing high-performance oxygen evolution reaction (OER) catalysts with low precious metal loadings for water electrolysis applications (e.g., for green hydrogen production) is challenging and requires electrically conductive, high-surface-area, and stable support materials. Combining the properties of stable TiO₂ with those of active iridium oxide, we synthesized highly active electrodes for OER in acidic media. TiO₂ powders (both commercially available Degussa P-25^® and hydrothermally prepared in the laboratory from TiOSO₄, either as received/prepared or following ammonolysis to be converted to titania black), were decorated with IrO₂ by UV photodeposition from Ir(III) aqueous solutions of varied methanol scavenger concentrations. TEM, EDS, FESEM, XPS, and XRD measurements demonstrate that the optimized version of the photodeposition preparation method (i.e., with no added methanol) leads to direct deposition of well-dispersed IrO₂ nanoparticles. The electroactive surface area and electrocatalytic performance towards OER of these catalysts have been evaluated by cyclic voltammetry (CV), Linear Sweep Voltammetry (LSV), and Electrochemical Impedance Spectroscopy (EIS) in 0.1 M HClO₄ solutions. All TiO₂-based catalysts exhibited better mass-specific (as well as intrinsic) OER activity than commercial unsupported IrO₂, with the best of them (IrO₂ on Degussa P-25^® ΤiO₂ and laboratory-made TiO₂ black) showing 100 mAmg_Ir⁻¹ at an overpotential of η = 243 mV. Chronoamperometry (CA) experiments also proved good medium-term stability of the optimum IrO₂/TiO₂ electrodes during OER.

Transparent supercapacitors find a large number of applications as components of many electronic devices and circuits. Mixed Ni–Co oxides (NCOs) are among the most promising supercapacitor electrode materials exhibiting high pseudo-capacitance and good electronic conductivity, while inkjet printing is a low cost and versatile technique for electrode printing. Surprisingly, although there have been many studies of NCO supercapacitor films on ITO glass substrates, these have not been prepared by the inkjet technique, and their optical properties were not fully characterized. Hereby, we report the fabrication and characterization of thin (295 and 477 nm thick; 0.017 and 0.035 mg cm⁻² NCO loading) semi-transparent NiCo₂O₄/ITO supercapacitor electrodes, showing transparency to visible light (60–30%, from the thinner to the thicker electrode layers tested), typical mass specific capacitance for NCO-based supercapacitor electrodes (1294–829 Fg⁻¹ at 1 mA cm⁻² discharge current density) and high volumetric capacitance (746–608 F cm⁻³ at 1 mA cm⁻²). The NCO nanoparticles were prepared by hydrothermal synthesis followed by thermal treatment and ball milling (ZrO₂ balls, 0.5 mm diameter), resulting in a cubic nickel–cobalt oxide structure and particle size in the 30–150 nm range, whereas the electrode layers were printed from water-propylene glycol solutions using a Dimatix DMP-2850 drop-on-demand (DoD) inkjet printer. Constant current charge–discharge experiments of the supercapacitor electrode (at ca 0.5 mA cm⁻²) for 1000 cycles confirmed stability of performance.