Radiation damage suppression in AISI-316 steel nanoparticles: Implications for the design of future nuclear materials

Publikationen: Beitrag in FachzeitschriftArtikelForschung(peer-reviewed)

Autoren

  • Emily Aradi
  • Jacob Lewis-Fell
  • Graeme Greaves
  • Stephen E. Donnelly
  • Jonathan A. Hinks

Externe Organisationseinheiten

  • University of Huddersfield
  • Universität Manchester

Abstract

The self-healing capability of point and extended defects that are introduced by energetic particle irradiation is a desired behavior to be attained in the design and selection in potential materials for application in extreme environments. Nanoporous materials have a potential for achieving higher radiation tolerance due to the presence of many active unsaturable surfaces to which defects may diffuse and thus be effectively annihilated. The effects of heavy ion collisions in the lattice of functional AISI-316 steel nanoparticles (NPs)-which serve as a model for the ligaments in a nanoporous-are herein investigated in situ within a transmission electron microscope. Comparisons are made directly with AISI-316 steel in the form of foils, and the results show that the fewer radiation-induced defect clusters form in the NPs and that small NPs (r < 50 nm) were observed to accumulate fewer defects when compared to larger NPs. Post-irradiation analytical characterization within a scanning transmission electron microscope revealed that the AISI-316 steel NPs may develop a radiation-induced self-passivation driven by a solute-drag mechanism: an effect that can potentially enhance their radiation corrosion resistance in the expected extreme conditions of a reactor. The capability of an NP to self-heal irradiation-induced point defects is investigated using the cellular model for active internal and surface sinks. The design of functional nanoscale materials for extreme environments is discussed.

Details

OriginalspracheEnglisch
Seiten (von - bis)9652-9662
Seitenumfang11
FachzeitschriftACS Applied Nano Materials
Jahrgang3
Ausgabenummer10
DOIs
StatusVeröffentlicht - 23 Okt. 2020