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The influence of different combinations of accelerated stress test (AST) protocols simulating load-cycle and start/stop conditions of a proton exchange membrane fuel cell (PEMFC) vehicle is investigated on a bimodal Pt/C catalyst. The bimodal Pt/C catalyst, prepared by mixing two commercial catalysts, serves as a model system and consists of two distinguishable size populations. The change in mean particle size was investigated by in situ small-angle X-ray scattering (SAXS). The comparison to the reference catalysts, i.e., the two single-size population catalysts, uncovers the presence of electrochemical Ostwald ripening as a degradation mechanism in the bimodal catalyst. Increasing the harshness of the applied AST protocol combinations by faster changing between load-cycle or start/stop conditions, the particle size of the larger population of the bimodal catalyst increases faster than expected. Surprisingly, the change in mean particle size of the smaller size population indicates a smaller increase for harsher AST protocols, which might be explained by a substantial electrochemical Ostwald ripening.

A metal-free oxygen reduction reaction (ORR) electrocatalyst with outstanding performance was obtained through an easy and one-pot synthesis of hemoglobin functionalized fructose@graphene-oxide (GO) nanocomposites. The active pyridinic nitrogen sites of the highly unfolded proteins together with the excellent electronic properties of GO appears to be the main factors causing the improved electrocatalytic activity.

The oxygen reduction (ORR) and hydrogen evolution (HER) reactions are the most important cathodic processes involved in fuel cell and water splitting technologies, respectively. The development of bifunctional electrocatalyst materials plays a key role in the rapid advancement of these hydrogen-based renewable energy strategies. This work proposes citrate-stabilized gold nanoparticles (AuNPs) as a bifunctional electrocatalyst for ORR and HER. The capping ligand has a great influence on their resulting electrocatalytic performance. A simple ligand exchange method based on concentration gradients has been optimized. The surface structure of the different ligand-stabilized AuNPs was inferred by lead underpotential deposition (Pb-UPD). Static and dynamic electrochemical studies for both ORR and HER have been performed using different ligand-stabilized AuNPs as electrocatalysts, demonstrating that the citrate ligand confers the best performance. This work suggests that non-doped chemically synthesized AuNPs may be suitable as a bifunctional electrocatalyst in fuel cells and hydrogen production.