Mixed oxide Ir-Sn-Sb-O electrocatalyst was synthesized using thermal decomposition from chloride precursors in ethanol. Our previous results showed that Ir-Sn-Sb-O possesses electrocatalytic activity for an oxygen evolution reaction (OER) in acidic media. In the present work, the physicochemical characterization and performance of Ir-Sn-Sb-O in an electrolysis cell are reported. IrO₂ supported on antimony doped tin oxide (ATO) was also considered in this study as a reference catalyst. Scanning electron microscopy (SEM) images indicated that Ir-Sn-Sb-O has a mixed morphology with nanometric size. Energy dispersive X-ray spectroscopy (EDS) showed a heterogeneous atomic distribution. Transmission electron microscopy (TEM) analysis resulted in particle sizes of IrO₂ and ATO between 3 to >10 nm, while the Ir-Sn-Sb-O catalyst presented non-uniform particle sizes from 3 to 50 nm. X-ray diffraction (XRD) measurements indicated that synthesized mixed oxide consists of IrO₂, IrO_x, doped SnO₂ phases and metallic Ir. The Ir-Sn-Sb-O mixed composition was corroborated by temperature programmed reduction (TPR) measurements. The performance of Ir-Sn-Sb-O in a single cell electrolyser showed better results for hydrogen production than IrO₂/ATO using a mechanical mixture. Ir-Sn-Sb-O demonstrated an onset potential for water electrolysis close to 1.45 V on Ir-Sn-Sb-O and a current density near to 260 mA mg⁻¹ at 1.8 V. The results suggest that the mixed oxide Ir-Sn-Sb-O has favorable properties for further applications in water electrolysers.

In this work, PtPd hybrid cathodic catalysts were prepared for a proton exchange membrane fuel cell (PEMFC) application by two different strategies. The first strategy was the physical mixing of bimetallic PtPd onto partially reduced graphene oxide (PtPd/rGO) and PtPd onto multi-walled carbon nanotubes (PtPd/MWCNT); (PtPd/rGO) + (PtPd/MWCNT). The second strategy was physical mixing of both carbonaceous supports before the PtPd deposition to form PtPd/(rGO:MWCNT). Our experimental results revealed that the PtPd nanomaterial prepared over a mixture of both carbonaceous supports had better oxygen reduction reaction (ORR) and PEMFC performances than the individually prepared catalysts. The insertion of MWCNT between rGO sheets prevented their stacking. This promoted the diffusion of oxygen molecules through the interlayer spacing, enhancing the ORR’s electrocatalytic activity. The durability test demonstrated that the hybrid supporting material dramatically improved the catalyst’s stability even after 3000 reaction cycles. This highlighted an increase greater than 100% for hybrid nanocomposites in their electrocatalytic activity as compared with the PtPd/rGO nanocomposite.

In this work, the synthesis of bimetallic Ag and Cu particles on carbon vulcan (AgCu/C) is reported, synthesized by a simple galvanic displacement method using citrate tribasic hydrate as a co-reducing agent and a commercial material based on Cu/C as a template. The materials were characterized by several physicochemical techniques, including TGA, ICP-OES, XRD, SEM, and BET. The catalysts were evaluated as cathodic catalysts for the oxygen reduction reaction (ORR) and were used for the preparation of membrane electrode assemblies for evaluation in an Anion Exchange Membrane Fuel Cell (AEMFC). The results were compared with the commercial Ag/C and Cu/C catalysts; the bimetallic catalyst obtained a higher power density, which was attributed to a synergistic effect between Ag and Cu particles.