Research on fuel cell technology is constantly gaining importance, while global emission requirements are becoming more and more restrictive. For environmentally neutral proton exchange membrane fuel cells (PEMFCs) to become a competitive technology, sustainable infrastructures need to be established. One of the main showstoppers is the utilization of the rare and therefore costly precious metal Pt as the key element in the electrocatalysis of hydrogen and oxygen. A huge amount of research is done on immensely reducing or even replacing Pt for future PEMFC technology. In this research update, the progress on oxygen reduction reaction catalysts in acidic media over the past two years is reviewed, with special attention to their durability.

Homogeneous mesoporous Ni-rich Ni–Pt thin films with adjustable composition have been synthesised by one-step micelle-assisted electrodeposition. The films exhibit a face-centred cubic solid solution (single phase) and their magnetic and mechanical properties can be tuned by varying the alloy composition. In particular, the Curie temperature (T_C) is shown to decrease with the Pt content and thin films with a T_C close to room temperature (i.e. Ni₅₈Pt₄₂) and below can be produced. Hysteresis loops show a decrease of saturation magnetisation (M_s) and coercivity (H_c) with decreasing Ni content. A comparison of porous and dense films reveals significantly lower saturation magnetic field strength for porous films. Concerning mechanical properties, mainly two trends can be observed: a decrease of the Young's modulus of the nanoporous films with respect to dense films by 10% in average and a progressive increase of Young's modulus with the Ni content from 4.2 GPa to 5.7 GPa in both types of films. The tunability of properties and facility of synthesis make this alloy a promising material for microelectromechanical systems (MEMS).

Ni-based bimetallic films with 20 at.% and 45 at.% Cu and mesostructured surfaces were prepared by electrodeposition from an aqueous solution containing micelles of P123 triblock copolymer serving as a structure-directing agent. The pH value of the electrolytic solution had a key effect on both the resulting Cu/Ni ratio and the surface topology. The catalytic activity of the CuNi films toward hydrogen evolution reaction was investigated by cyclic voltammetry (CV) in 1 M KOH electrolyte at room temperature. The Cu₄₅Ni₅₅ film showed the highest activity (even higher than that of a non-mesostructured pure Ni film), which was attributed to the Ni content at the utmost surface, as demonstrated by CV studies, as well as the presence of a highly corrugated surface.