Core-shell and heterostructured silver-nickel nanocatalysts fabricated by γ-radiation induced synthesis for oxygen reduction in alkaline media.

To reach commercial viability for fuel cells, one needs to develop active and robust Pt-free electrocatalysts. Silver has great potential to replace Pt as the catalyst for the oxygen reduction reaction (ORR) in alkaline media due to its low cost and superior stability. However, its catalytic activity needs to be improved. One possible solution is to fabricate bimetallic nanostructures, which demonstrate a bifunctional enhancement in the electrochemical performance. Here, two types of bimetallic silver-nickel nanocatalysts, core-shells (Ag@NiO) and heterostructures (Ag/Ni), are fabricated using γ-radiation induced synthesis. The Ag@NiO nanoparticles consist of an amorphous, NiO layer as a shell and a facetted crystalline Ag particle as a core. Meanwhile, the Ag/Ni heterostructures comprise Ag particles decorated with Ni/Ni(oxy-hydro)-oxide clusters. Both materials demonstrate similar and increased alkaline ORR activity as compared to monometallic catalysts. It was revealed that the enhanced catalytic activity of the core-shells is mainly attributed to the electronic ligand effect. While in the Ag/Ni heterostructures, a lattice mismatch between the Ni-based clusters and Ag implies a significant lattice strain, which, in turn, is responsible for the increased activity of the catalyst. Also, the Ag/Ni samples exhibit good stability under operating conditions due to the existence of stable Ni 3+ compounds on the surface.