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1.
Faraday Discuss ; 138: 181-92; discussion 211-23, 433-4, 2008.
Artigo em Inglês | MEDLINE | ID: mdl-18447016

RESUMO

The magnetism of Co-Rh nanoparticles is investigated experimentally and theoretically. The particles (approximately 2 nm) have been synthesized by decomposition of organometallic precursors in mild conditions of pressure and temperature, under hydrogen atmosphere and in the presence of a polymer matrix. The magnetic properties are determined by SQUID, Mössbauer spectroscopy, and X-ray magnetic circular dichroism (XMCD). The structural and chemical properties are characterized by wide angle X-ray scattering, transmission electronic microscopy and X-ray absorption near edge spectroscopy. All the studied Co-Rh clusters are magnetic with an average spin moment per atom mu that is larger than the one of macroscopic crystals or alloys with similar concentrations. The experimental results and comparison with theory suggest that the most likely chemical arrangement is a Rh core, with a Co-rich outer shell showing significant Co-Rh mixing at the interface. Measured and calculated magnetic anisotropy energies (MAEs) are found to be higher than in pure Co clusters. Moreover, one observes that the MAEs can be tuned to some extent by varying the Rh concentration. These trends are well accounted for by theory, which in addition reveals important spin and orbital moments induced at the Rh atoms as well as significant orbital moments at the Co atoms. These play a central role in the interpretation of experimental data as a function of Co-Rh content. A more detailed analysis from a local perspective shows that the orbital and spin moments at the Co-Rh interface are largely responsible for the enhancement of the magnetic moments and magnetic anisotropy.

2.
Phys Rev Lett ; 91(19): 197206, 2003 Nov 07.
Artigo em Inglês | MEDLINE | ID: mdl-14611612

RESUMO

Layer-resolved self-consistent electronic calculations of magnetic anisotropy energy (MAE) provide new insight to the off-plane magnetization observed in Pd capped Co films on Pd(111). We demonstrate that the transition from perpendicular to in-plane phases with increasing film thickness involves an intermediate spin-canted phase. The interfaces responsible for the stability of the off-plane easy axes are characterized microscopically. A local analysis of the MAEs reveals an unexpected internal magnetic structure of the Co-Pd interfaces in which the magnetic moments and spin-orbit interactions at the Pd atoms play a crucial role.

3.
Phys Rev Lett ; 90(22): 226402, 2003 Jun 06.
Artigo em Inglês | MEDLINE | ID: mdl-12857328

RESUMO

The local and average orbital moments of transition-metal (TM) clusters are determined bridging the gap between atomic Hund's rules and solid-state quenching. A remarkable enhancement of is revealed in agreement with recent measurements. In small Ni(N) (N< or =10), represents (20-40)% of the total magnetization and is therefore crucial for the comparison between theory and experiment. Larger clusters (N> or =150) show nearly bulklike quenching at the interior but retain a considerable surface enhancement. Trends for different TM's are discussed.

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