Thermodynamics of hydride formation: Anisotropic size-dependent coupled chemo-thermo-mechanical effects at Ni/NiH interfaces

Ni nanoparticles are frequently used as catalysts for hydrogenation reactions as well as in hydrogen storage applications. Recently, we have shown that small Ni nanoparticles can absorb hydrogen at < 10 bar pressure to form Ni hydride. During this process, the hydride growth is anisotropic, and a coherent Ni/NiH interface is formed. In order to explain the anisotropy and to comprehensively account for the coupling chemical, mechanical and thermal effects, we develop in this study a simplified chemo-thermo-mechanical enthalpy model for Ni/NiH interfaces in thin films. This model captures the combined influence of extent of hydride formation x, temperature T, pressure P, size effect ($l$), and the ${\alpha}$/${\beta}$ interface energy ${\lambda}$. Two different ${\alpha}$/${\beta}$ interface orientations, namely (100) and (111), are investigated. The model is shown to correctly predict the enthalpy and volume changes over a wide range of length scales, from atomically thin layers (~1 nm) to micron scale and larger. This work provides the basis for the development of similar enthalpy models for other solid-state hydrogen storage nanostructured materials where anisotropic growth of hydride phases is also observed.