The average and local structure of TiVCrNbDx (x=0,2.2,8) from total scattering and neutron spectroscopy

• Published in: Acta materialia 2021-02, Vol.205, Article 116496
• Main Authors: Nygård, Magnus M., Fjellvåg, Øystein S., Sørby, Magnus H., Sakaki, Kouji, Ikeda, Kazutaka, Armstrong, Jeff, Vajeeston, Ponniah, Sławiński, Wojciech A., Kim, Hyunjeong, Machida, Akihiko, Nakamura, Yumiko, Hauback, Bjørn C.
• Format: Article
• Language: English
• Subjects: HEAs; High-entropy alloys; Hydrogen storage; Inelastic neutron scattering; INS; Metal hydrides; Reverse Monte Carlo; RMC; Total scattering
• ISSN: 1359-6454; 1873-2453
• DOI: 10.1016/j.actamat.2020.116496

[Display omitted] The volumetric hydrogen density of 160 kg H/m3 in TiVCrNbH8 is among the highest for interstitial hydrides, but the reported reversible capacity is only about 2/3 of the full theoretical capacity at room temperature. In the present work we have investigated the local structure in TiVCrNbDx,x=0, 2.2, 8 with the aim to unravel how the remaining sites can be destabilized with respect to hydrogen/deuterium occupation using total scattering measurements and Reverse Monte Carlo (RMC) structure modelling. Our analysis indicates that the partially desorbed deuteride (x=2.2) adopts a body-centred tetragonal structure (I4/mmm) where the deuterium atoms occupy both tetrahedral and octahedral interstices with low occupancies. There is a significantly higher portion of occupied sites with nearest-neighbour metals with low valence-electron concentration VEC. This observation is used to motivate strategies for further destabilization of the hydride. Inelastic neutron scattering (INS) and density functional theory (DFT) calculations indicate that the vibrational density of states is very diverse in TiVCrNbH2.4, and it is suggested that the hydrogen atoms might be mobile between nearby interstices.