RESUMEN
Photocatalysis is essential for wastewater cleanup and clean energy, and in this current study, we have synthesized nanomaterials (iron oxide-based) for photocatalytic pollution degradation and hydrogen production. The performance of aluminium oxide/ferric oxide (Al2O3/Fe2O3), samarium oxide/ferric oxide (Sm2O3/Fe2O3) and yttrium oxide/ferric oxide (Y2O3/Fe2O3) were compared for the production of hydrogen (H2) and degradation of dye under natural sunlight. Various characterisation equipment was used to characterize these photocatalysts' structure, morphology, elemental content, binding energy and band gap. The hydrogen recovery efficiency of iron oxide-based photocatalysts from sulphide-containing wastewater is assessed. Y2O3/Fe2O3 has shown the highest hydrogen production of 340 mL/h. The influence of operating factors such as sulphide ion concentration, catalyst quantity, and photocatalyst photolytic solution volume on hydrogen production is studied. The optimal values were 0.25 M, 0.2 g/L, and 1L, respectively. The developed photocatalyst passed multiple cycles of stability testing. Fe2O3 has shown the highest Rhodamine B (RhB) dye degradation efficiency of 94% under visible light.
RESUMEN
Development of electrocatalysts with extended homogeneity and improved metal-support interactions is of urgent scientific need in the context of electrochemical energy applications. Herein, bimetallic Pt-Pd nanoparticles with good homogeneity are fabricated using a convenient solution phase chemical reduction method onto a reduced graphene oxide (rGO) support. X-ray diffraction studies revealed that Pt-Pd/rGO possesses the crystallite size of 3.1 nm. The efficacies of Pt-Pd/rGO catalyst (20 wt% Pt + 10 wt% Pd on rGO support, Pt:Pd atomic ratio = 1:1) towards ethanol electrooxidation reaction (EOR) are evaluated in acidic conditions by cyclic voltammetry using catalyst-coated glassy carbon electrode as a working electrode. With the better dispersion on rGO support the Pt-Pd/rGO nancomposite catalyst exhibit highest mass specific activity (0.358 mA/µg-Pt) which is observed to be 1.9 times of similarly synthesized 20 wt% Pt/rGO (0.189 mA/µg-Pt) and 2.5 times of commercial 20 wt% Pt/C (0.142 mA/µg-Pt), respectively. Apart from the observed improved EOR activity, the Pt-Pd/rGO catalyst exhibited better stability than Pt/rGO and Pt/C catalysts. Strong synergy offered by Pt, Pd and rGO support could contribute to the observed higher EOR activity of Pt-Pd/rGO.