Abstract
Abstract We studied the α 虠 γ phase transformation in Fe and Fe-Au thin films and nanoparticles employing in situ X-ray diffraction by varying the temperature (from room temperature up to 1100 °C), film thickness, particle size and composition. In pure Fe particles the transformation did not occur, whereas in the respective thin films a "reverse size effect" was observed - only the thinnest and the thickest films underwent the transformation. In contrast, the γ-Fe phase was observed in all Fe-Au samples (bi-particles and thin films), and remained metastable at room temperature. γ-Fe particles as large as 300 nm were observed by electron microscopy. The results are discussed in terms of the difference in available nucleation sites in the particles, bi-particles and films; critical nucleus size and nucleation energy barrier; and the facilitating presence of Fe/Au interfaces. The reverse size effect challenges the paradigm that phase stability at the nanoscale changes monotonously with a decrease of the system's characteristic dimensions.
| Original language | English |
|---|---|
| Article number | 12300 |
| Pages (from-to) | 343-354 |
| Number of pages | 12 |
| Journal | Acta Materialia |
| Volume | 98 |
| DOIs | |
| State | Published - 1 Oct 2015 |
Keywords
- In situ X-ray diffraction
- Nanoparticles
- Phase transformations
- Size effect
- Thin films
All Science Journal Classification (ASJC) codes
- Electronic, Optical and Magnetic Materials
- Ceramics and Composites
- Polymers and Plastics
- Metals and Alloys