Journal
JOURNAL OF APPLIED PHYSICS
Volume 120, Issue 8, Pages -Publisher
AMER INST PHYSICS
DOI: 10.1063/1.4961607
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Funding
- National Science Foundation (NSF), DMR [DMR-1454618]
- NSF, DMR [DMREF: SusChEM 1436385]
- National Science Foundation of China (NSFC) [51272209, 51471125, 51501140]
- Shaanxi Province Science and Technology Innovation Team Project [2013KCT-05]
- Division Of Materials Research
- Direct For Mathematical & Physical Scien [1454618] Funding Source: National Science Foundation
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We have studied the kinetics of the transitions between the Fe2O3 and Fe3O4 phases as thin epilayers (similar to 2.5 nm) on Al2O3 (001) substrates using time-resolved reflection high energy electron diffraction. The different iron oxide phases were identified using a combination of in-situ and ex-situ characterizations. The transition from an alpha-Fe2O3 (001) epilayer to a Fe3O4 (111) epilayer through thermal reduction was found to be determined by the Fe-O bonding energy, resulting in a long time scale. The oxidation at high temperature converts a Fe3O4 (111) epilayer to an alpha-Fe2O3 (001) epilayer quickly; at low temperature, a gamma-Fe2O3 (111) epilayer was slowly generated instead. By repeating the deposition/thermal reduction processes, a thicker Fe3O4 (111) film was obtained, which exhibit high crystallinity and moderate magnetic coercivity. Published by AIP Publishing.
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