4.6 Article

Phase Discrimination through Oxidant Selection in Low-Temperature Atomic Layer Deposition of Crystalline Iron Oxides

Journal

LANGMUIR
Volume 29, Issue 10, Pages 3439-3445

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/la305027k

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Funding

  1. ANSER Center
  2. Energy Frontier Research Center
  3. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-SC0001059]
  4. U.S. Department of Energy, Office of Basic Energy Sciences
  5. U.S. Department of Energy Office of Science Laboratory [DE-AC02-06CH11357]

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Control over the oxidation state and crystalline phase of thin-film iron oxides was achieved by low-temperature atomic layer deposition (ALD), utilizing a novel iron precursor, bis(2,4-methylpentadienyl)iron. This low-temperature (T = 120 degrees C) route to conformal deposition of crystalline Fe3O4 or alpha-Fe2O3 thin films is determined by the choice of oxygen source selected for the second surface half-reaction. The approach employs ozone to produce fully oxidized alpha-Fe2O3 or a milder oxidant, H2O2, to generate the Fe2+/Fe3+ spinel, Fe3O4. Both processes show self-limiting surface reactions and deposition rates of at least 0.6 angstrom/cycle, a significantly high growth rate at such mild conditions. We utilized this process to prepare conformal iron oxide thin films on a porous framework, for which alpha-Fe2O3 is active for photocatalytic water splitting.

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