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F. Aguilera-Granja

Publications and source records attributed to F. Aguilera-Granja.

4 recordsLinked to original sources

Non-Collinearity in Small Magnetic Cobalt-Benzene Molecules

Organometallic clusters based on transition metal atoms are interesting because possible applications in spintronics and quantum information. In addition to the enhanced magnetism at the nanoscale, the organic ligands may provide a natural shield again unwanted magnetic interactions with the matrices required for applications. Here we show that the organic ligands may lead to non-collinear magnetic order as well as the expected quenching of the magnetic moments. We use different density functional theory (DFT) methods to study the experimentally relevant three cobalt atoms surrounded by benzene rings (Co$_3$Bz$_3$). We found that the benzene rings induce a ground state with non-collinear magnetization, with the magnetic moments localized on the cobalt centers and lying on the plane formed by the three cobalt atoms. We further analyze the magnetism of such a cluster using an anisotropic Heisenberg model where the involved parameters are obtained by a comparison with the DFT results. These results may also explain the recent observation of null magnetic moment of Co$_3$Bz$_3^+$. Moreover, we propose an additional experimental verification based on electron paramagnetic resonance.

physics.chem-ph

Collinear versus non-collinear magnetic order in Pd atomic clusters: ab-initio calculations

We present a thorough theoretical assessment of the stability of non-collinear spin arrangements in small palladium clusters. We generally find that ferromagnetic order is always preferred, but that antiferromagnetic and non-collinear configurations of different sorts exist and compete for the first excited isomers. We also show that the ground state is insensitive to the choice of atomic configuration for the pseudopotential used and to the approximation taken for the exchange and correlation potential. Moreover, the existence and relative stability of the different excited configurations also depends weakly on the approximations employed. These results provide strong evidence on the transferability of pseudopotential and exchange and correlation functionals for palladium clusters as opposed to the situation found for the bulk phases of palladium.

cond-mat.mtrl-sci

Collinear versus non-collinear magnetic order in Pd atomic clusters

We present a thorough theoretical assessment of the stability of non-collinear spin arrangements in small palladium clusters. We generally find that ferromagnetic order is always preferred, but that antiferromagnetic and non-collinear configurations of different sorts exist and compete for the first excited isomers. We also show that the relative stability of all these states is rather insensitive to the choice of atomic configuration for the pseudopotential used and to the approximation taken for the exchange and correlation potential. This result stands in stark contrast with the situation found for the bulk phases of palladium.

cond-mat.mtrl-sci

Theory for the reduction of products of spin operators

In this study we show that the sum of the powers of arbitrary products of quantum spin operators such as $(S^+)^l(S^-)^m(S^z)^n$ can be reduced by one unit, if this sum is equal to 2S+1, S being the spin quantum number. We emphasize that by a repeated application of this procedure \em all \em arbitrary spin operator products with a sum of powers larger than 2S can be replaced by a combination of spin operators with a maximum sum of powers not larger than 2S. This transformation is exact. All spin operators must belong to the same lattice site. By use of this procedure the consideration of single-ion anisotropies and the investigation of the magnetic reorientation within a Green's function theory are facilitated. Furthermore, it may be useful for the study of time dependent magnetic properties within the ultrashort (fsec) time domain.

cond-mat.str-el