Abstract
Atomic mixing by replacement collision sequences and other cascade effects is well known to create chemical disorder in irradiated alloys. Most studies of irradiation-induced disordering have focused on ex situ analysis of irradiated samples; however, fast in situ techniques are necessary to measure disordering at elevated temperatures without significant interference from concurrent re-ordering processes. In the present work, we use in situ electron diffraction with high speed data collection to measure the initial change in the long-range order parameter S with ion dose φ during 500 keV Ne+ irradiation of Cu3Au foils. The data reveal an unexpected and dramatic increase in the disordering rate as the critical order-disorder transition temperature TC is approached. Molecular dynamics simulations show that this increase is not due to temperature-dependent cascade mixing. We attribute the enhanced disordering, instead, to coupling between point defect fluxes and the chemical state of order.
| Original language | English |
|---|---|
| Pages (from-to) | 3841-3848 |
| Number of pages | 8 |
| Journal | Journal of Materials Research |
| Volume | 33 |
| Issue number | 22 |
| DOIs | |
| State | Published - Nov 28 2018 |
| Externally published | Yes |
Keywords
- defects
- radiation effects
- transmission electron microscopy (TEM)