In Situ Atomic-Scale Observation of Phase Evolution in Nickel Phosphide Nanoparticles

High Resolution Image Download MS PowerPoint Slide Nickel phosphides are promising earth-abundant, low-cost catalysts for hydrogen/oxygen evolution reactions and CO 2 reduction. However, their formation mechanisms remain poorly understood and difficult to control. This particularly applies to mechanisms determining phase evolution, crystallinity, and morphology under reactive conditions, factors that critically influence catalytic activity and stability. Here, we employ environmental transmission electron microscopy to directly observe the conversion of nickel nanoparticles into nickel phosphide phases under controlled phosphine atmosphere and temperatures. A three-stage Ni-to-Ni 2 P conversion sequence is observed: (i) surface nucleation, (ii) rapid particle-size expansion, and (iii) crystallographic restructuring and faceting. Phase selectivity depends on the phosphine pressure and temperature: Ni 2 P forms at both low and high pressures, Ni 2 P and Ni 5 P 4 coexist at intermediate pressure, and Ni 12 P 5 emerges under no phosphine supply (residual phosphine may have remained) at elevated temperatures. We capture the temperature-driven Ni 2 P-to-Ni 12 P 5 transition. These insights offer strategies to control the phase and morphology for improved catalytic performance.