Phase transformation in an yttrium–hydrogen system studied by TEM / K. Wang in Acta materialia, Vol. 58 N° 7 (Avril 2010)  

Public ISBD [article]  inActa materialia > Vol. 58 N° 7 (Avril 2010) . - pp. 2585–2597 Titre : Phase transformation in an yttrium–hydrogen system studied by TEM Type de document : texte imprimé Auteurs : K. Wang, Auteur ; J.R. Hattrick-Simpers, Auteur ; L. A. Bendersky, Auteur Année de publication : 2011 Article en page(s) : pp. 2585–2597 Note générale : Métallurgie Langues : Anglais (eng) Mots-clés : Yttrium hydride Phase transformation Thin-films TEM Ordering of hydrogen Résumé : Phase transformations in Pd-capped epitaxial yttrium films grown on (0 0 0 1) sapphire substrates covered with a Ti buffer layer and hydrogenated for different times were studied using transmission electron microscopy (TEM). For short hydrogen charging times, the phase transformation from α-Y to β-YH2 is associated with the nucleation and growth of two orientational variants, which after coalescence form twin-related lamellae of the β-YH2 phase with twin interfaces parallel to the substrate plane. Shockley partial dislocations are present at the twin boundaries; their glides during phase transformation are responsible for the formation of the twin lamellae. Superlattice reflections were observed for β-YH2, and the existence of a new long-range ordered superstoichiometric YH2+x phase was suggested. A structural model of the ordering based on the occupation of octahedral interstitial sites by H in a doubled cell of Y-face-centered cubic was offered. For samples hydrogenated for longer times, β-YH2-to-γ-YH3 phase transformation was accompanied by cracking along the twin boundaries, which eventually developed into a network of pores and caused significant swelling of the films. No γ-YH3 phase was observed directly in TEM because of its unstable nature under the high vacuum of a microscope column. The fully transformed YH3 films have over a 60% increase in its thickness, which is mostly accounted for by the high volume fraction of pores. DEWEY : 669 ISSN : 1359-6454 En ligne : http://www.sciencedirect.com/science/article/pii/S1359645409009033 [article] Phase transformation in an yttrium–hydrogen system studied by TEM [texte imprimé] / K. Wang, Auteur ; J.R. Hattrick-Simpers, Auteur ; L. A. Bendersky, Auteur . - 2011 . - pp. 2585–2597. Métallurgie Langues : Anglais (eng) in Acta materialia > Vol. 58 N° 7 (Avril 2010) . - pp. 2585–2597 Mots-clés : Yttrium hydride Phase transformation Thin-films TEM Ordering of hydrogen Résumé : Phase transformations in Pd-capped epitaxial yttrium films grown on (0 0 0 1) sapphire substrates covered with a Ti buffer layer and hydrogenated for different times were studied using transmission electron microscopy (TEM). For short hydrogen charging times, the phase transformation from α-Y to β-YH2 is associated with the nucleation and growth of two orientational variants, which after coalescence form twin-related lamellae of the β-YH2 phase with twin interfaces parallel to the substrate plane. Shockley partial dislocations are present at the twin boundaries; their glides during phase transformation are responsible for the formation of the twin lamellae. Superlattice reflections were observed for β-YH2, and the existence of a new long-range ordered superstoichiometric YH2+x phase was suggested. A structural model of the ordering based on the occupation of octahedral interstitial sites by H in a doubled cell of Y-face-centered cubic was offered. For samples hydrogenated for longer times, β-YH2-to-γ-YH3 phase transformation was accompanied by cracking along the twin boundaries, which eventually developed into a network of pores and caused significant swelling of the films. No γ-YH3 phase was observed directly in TEM because of its unstable nature under the high vacuum of a microscope column. The fully transformed YH3 films have over a 60% increase in its thickness, which is mostly accounted for by the high volume fraction of pores. DEWEY : 669 ISSN : 1359-6454 En ligne : http://www.sciencedirect.com/science/article/pii/S1359645409009033

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