4.7 Article

The Effect of A-Site Substitution of Ce and La on the Magnetic and Electronic Properties of Sr(Ti0.6Fe0.4)O3-δ Films

Journal

INORGANIC CHEMISTRY
Volume 51, Issue 24, Pages 13245-13253

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ic301726w

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Funding

  1. National Science Foundation, Division of Materials Research
  2. Chinese Scholarship Council
  3. National Science Foundation [DMR-0819762]
  4. Direct For Mathematical & Physical Scien
  5. Division Of Materials Research [1104912] Funding Source: National Science Foundation

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The structure and magnetic properties of epitaxial (CexSr1-x)(Ti0.6Fe0.4)O3-delta (x = 0, 0.1, 0.2 and 0.3) and (LaxSr1-x)(Ti0.6Fe0.4)O3-delta (x = 0, 0.1, 0.2, 0.3 and 0.4) perovskite-structure thin films deposited by pulsed laser deposition on (LaAlO3)(0.3)(Sr2AlTaO6)(0.7) (LSAT) substrates are reported. Both La and Ce ions showed a dominant 3+ valence state and acted as donors on the Sr2+ site (A site) in the perovskite lattice. The optical band gap widened, and the Fermi level moved toward the vacuum level with increased Ce or La content; meanwhile the Ti and particularly the Fe ions were driven to a lower valence state, resulting in a higher Fe2+ concentration. The materials were magnetic at room temperature with up to 0.8 mu(B)/Fe and a magnetoelastic out-of-plane anisotropy. Ce and La lowered the coercivity while raising both the Faraday rotation at 1550 nm and the optical absorption at near-infrared wavelengths.

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