Published February 2017 | Version v1
Journal article

Relaxation path of metastable nanoclusters in oxide dispersion strengthened materials

  • 1. DEN-Service de Recherches Métallurgiques Appliquées, CEA, Université Paris-Saclay, F-91191, Gif-sur-Yvette (France)
  • 2. LLB, CEA, CNRS, Université Paris-Saclay, CEA Saclay, 91191, Gif-sur-Yvette (France)
  • 3. UMET, CNRS/UMR 8207, Bât. C6, Univ. Lille 1, 59655 Villeneuve d'Ascq (France)

Description

ODS steels are a promising class of structural materials for sodium cooled fast reactor application. The ultra-high density of the strengthening nanoclusters dispersed within the ferritic matrix is responsible of the excellent creep properties of the alloy. Fine characterization of the nanoclusters has been conducted on a Fe-14Cr-0.3Ti-0.3Y2O3 ODS material using High Resolution and Energy Filtered Transmission Electron Microscopy. The nanoclusters exhibit a cubic symmetry possibly identified as f.c.c and display a non-equilibrium YTiCrO chemical composition thought to be stabilized by a vacancy supersaturation. These nanoclusters undergo relaxation towards the Y2Ti2O7-like state as they grow. A Cr shell is observed around the relaxed nano-oxides, this size-dependent shell may form after the release of Cr by the particles. The relaxation energy barrier appears to be higher for the smaller particles probably owing to a volume/surface ratio effect in reason to the full coherency of the nanoclusters. - Highlights: • The nanoclusters display a f.c.c. cubic symmetry and a non-equilibrium YTiCrO chemical composition. • During thermal annealing the coherent nanocluster transform into semi-coherent pyrochlore particles. • A Cr ring is observed around the relaxed pyrochlore type particles.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jnucmat.2016.12.007

Additional details

Identifiers

DOI
10.1016/j.jnucmat.2016.12.007;
PII
S0022-3115(16)30927-8;

Publishing Information

Journal Title
Journal of Nuclear Materials
Journal Volume
484
Journal Page Range
p. 183-192
ISSN
0022-3115
CODEN
JNUMAM

Optional Information

Copyright
Copyright (c) 2016 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.