4.8 Article

Surfactant Organic Molecules Restore Magnetism in Metal-Oxide Nanoparticle Surfaces

Journal

NANO LETTERS
Volume 12, Issue 5, Pages 2499-2503

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/nl300665z

Keywords

Ferrites; metal-oxide nanoparticles; magnetism; electron magnetic chiral dichroism; electron energy loss spectroscopy

Funding

  1. Materials Sciences and Engineering Division of the U.S. Department of Energy (DOE)
  2. ERC [239739 STEMOX]
  3. Spanish MEC [2007-0086]
  4. U.S. DOE [DE-FG02-09ER46554]
  5. McMinn Endowment
  6. Spanish MICINN [MAT2009-08667, CSD2006-00012]
  7. Catalan DIUE [2009SGR856]
  8. National Center for Supercomputing Applications (U.S. Department of Energy) [DE-AC02-05CH11231]

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The properties of magnetic nanoparticles tend to be depressed by the unavoidable presence of a magnetically inactive surface layer. However, outstanding magnetic properties with a room-temperature magnetization near the bulk value can be produced by high-temperature synthesis methods involving capping with organic acid. The capping molecules are not magnetic, so the origin of the enhanced magnetization remains elusive. In this work, we present a real-space characterization on the subnanometer scale of the magnetic, chemical, and structural properties of iron-oxide nanoparticles via aberration-corrected scanning transmission electron microscopy. For the first time, electron magnetic chiral dichroism is used to map the magnetization of nanoparticles in real space with subnanometer spatial resolution. We find that the surface of the nanoparticles is magnetically ordered. Combining the results with density functional calculations, we establish how magnetization is restored in the surface layer. The bonding with the acid's O atoms results in O- Fe atomic configuration and distances close to bulk values. We conclude that the nature and number of molecules in the capping layer is an essential ingredient in the fabrication of nanoparticles with optimal magnetic properties.

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