Optimizing Hydrogen Storage Pathways in Ti–Al Alloys through Controlled Oxygen Addition

In the present study, we aimed to destabilize the Ti–Al system with nonmetallic oxygen. The synthesis of α-(Ti, Al)[O] starting from TiO2, Ti, and Al was carried out through the arc melting method, resulting in three different oxygen content levels, 3.4, 10, and 20 at%. The room temperature activati...

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Published inInternational journal of energy research Vol. 2024
Main Authors Shukla, Vivek, Han, Sung Ju, Ha, Taejun, Padhee, Satya Prakash, Jin-Yoo, Suh, Cho, Young Whan, Young-Su, Lee
Format Journal Article
LanguageEnglish
Published Bognor Regis Hindawi Limited 26.08.2024
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Summary:In the present study, we aimed to destabilize the Ti–Al system with nonmetallic oxygen. The synthesis of α-(Ti, Al)[O] starting from TiO2, Ti, and Al was carried out through the arc melting method, resulting in three different oxygen content levels, 3.4, 10, and 20 at%. The room temperature activation of α-(Ti, Al)[O] was not successful, and the activation was performed at 300°C under 5 MPa H2 pressure. The structural changes after hydrogenation (maximum absorption capacity of 3.74 wt% hydrogen) arose from the transformation of α-(Ti, Al)[O] to cubic (Ti, Al)[O]Hx (c-(Ti, Al)[O]Hx); nonetheless, they recovered their original lattice parameters, which are meaningfully larger than those of α-Ti, after dehydrogenation. The hydrogen storage capacities for various α-(Ti, Al)[O] compositions generally decreased with increasing oxygen (3.4 and 10 at%) and aluminum content in the alloy. In contrast, for the compositions with a higher oxygen content of 20 at%, the hydrogen storage capacity slightly increased as the Al concentration increased: Ti0.790Al0.010O0.200 absorbed 2.91 wt% hydrogen, whereas Ti0.767Al0.033O0.200 absorbed 3.04 wt% hydrogen. The thermogravimetric analysis showed that samples with 20 at% O released hydrogen at lower temperatures even though the major phase after hydrogenation is c-(Ti, Al)[O]Hx regardless of the oxygen content.
ISSN:0363-907X
1099-114X
DOI:10.1155/2024/2216181