Pathways of hydrogen atom diffusion at fcc Cu: Σ9 and Σ5 grain boundaries vs single crystal

• Published in: Journal of materials science Vol. 58; no. 44; pp. 17004 - 17018
• Main Authors: Lousada, Cláudio M., Korzhavyi, Pavel A.
• Format: Journal Article
• Language: English
• Published: New York Springer US 01.11.2023; Springer Nature B.V
• Subjects: Atomic structure; Characterization and Evaluation of Materials; Chemical reactions; Chemistry and Materials Science; Classical Mechanics; Computation & Theory; Coordination numbers; Crystal defects; Crystallography and Scattering Methods; Grain boundaries; Hydrogen atoms; Materials Science; Parameters; Polymer Sciences; Single crystals; Solid Mechanics; Symmetry; Tessellation; Tortuosity; Voronoi graphs
• ISSN: 0022-2461; 1573-4803; 1573-4803
• DOI: 10.1007/s10853-023-09032-y

The diffusion of H-atoms is relevant for innumerous physical–chemical processes in metals. A detailed understanding of diffusion in a polycrystalline material requires the knowledge of the activation energies (Δ E a ’s) for diffusion at different defects. Here, we report a study of the diffusion of H-atoms at the Σ9 and Σ5 grain boundaries (GBs) of fcc Cu that are relevant for practical applications of the material. The complete set of possible diffusion pathways was determined for each GB and we compared the Δ E a at bulk fcc Cu with the landscape of Δ E a ’s at these defects. We found that while a number of diffusion pathways at the GBs have high tortuosity, there are also many paths with very low tortuosity because of specific structural features of the interstitial GB sites. These data show that the diffusion of H-atoms at these GBs is highly directional but can be fast because at certain paths the Δ E a can be as low as 0.05 eV. The lowest energy paths for diffusion of H-atoms through the whole GB models are Δ E a  = 0.05 eV for the Σ9 and Δ E a  = 0.20 eV at Σ5 which compare with Δ E a  = 0.42 eV for the bulk fcc crystal. This shows that H-atoms will be able to diffuse very fast at these defects. With the Laguerre–Voronoi tessellation method, we studied how the local atomic structure of the interstitial sites of the GBs leads to different Δ E a ’s for diffusion of H-atoms. We found that the volume expansions and the coordination numbers alone cannot account for the magnitude of the Δ E a ’s. Hence, we developed a symmetry quantifying parameter that measures the deviation of symmetry of the GB sites from that of the bulk octahedral site and hence accounts for the distortion at the GB site. Only when this parameter is introduced together with the volume expansions and the coordination numbers, it is possible to correlate the local structure with the Δ E a ’s and to obtain descriptors of diffusion. The complete set of data shows that the extrapolation of diffusion data for H-atoms between different types of GBs is non-trivial and should be done with care.