arXiv subjects

S. Lounis

Publications and source records attributed to S. Lounis.

22 records · Page 2Linked to original sources

arXiv2010

Theory of Local Dynamical Magnetic Susceptibilities from the Korringa-Kohn-Rostoker Green Function Method

Within the framework of time-dependent density functional theory combined with the Korringa-Kohn-Rostoker Green function formalism, we present a real space methodology to investigate dynamical magnetic excitations from first-principles. We set forth a scheme which enables one to deduce the correct effective Coulomb potential needed to preserve the spin-invariance signature in the dynamical susceptibilities, i.e. the Goldstone mode. We use our approach to explore the spin dynamics of 3d adatoms and different dimers deposited on a Cu(001) with emphasis on their decay to particle-hole pairs.

cond-mat.mes-hall↗

arXiv2010

Spin Orbit Coupling and Spin Waves in Ultrathin Ferromagnets: The Spin Wave Rashba Effect

We present theoretical studies of the influence of spin orbit coupling on the spin wave excitations of the Fe monolayer and bilayer on the W(110) surface. The Dzyaloshinskii-Moriya interaction is active in such films, by virtue of the absence of reflection symmetry in the plane of the film. When the magnetization is in plane, this leads to a linear term in the spin wave dispersion relation for propagation across the magnetization. The dispersion relation thus assumes a form similar to that of an energy band of an electron trapped on a semiconductor surfaces with Rashba coupling active. We also show SPEELS response functions that illustrate the role of spin orbit coupling in such measurements. In addition to the modifications of the dispersion relations for spin waves, the presence of spin orbit coupling in the W substrate leads to a substantial increase in the linewidth of the spin wave modes. The formalism we have developed applies to a wide range of systems, and the particular system explored in the numerical calculations provides us with an illustration of phenomena which will be present in other ultrathin ferromagnet/substrate combinations.

cond-mat.mes-hall↗

arXiv2005

Non-collinear Korringa-Kohn-Rostoker Green function method: Application to 3d nanostructures on Ni(001)

Magnetic nanostructures on non-magnetic or magnetic substrates have attracted strong attention due to the development of new experimental methods with atomic resolution. Motivated by this progress we have extended the full-potential Korringa-Kohn-Rostoker (KKR) Green function method to treat non-collinear magnetic nanostructures on surfaces. We focus on magnetic 3d impurity nanoclusters, sitting as adatoms on or in the first surface layer on Ni(001), and investigate the size and orientation of the local moments and moreover the stabilization of non-collinear magnetic solutions. While clusters of Fe, Co, Ni atoms are magnetically collinear, non-collinear magnetic coupling is expected for Cr and Mn clusters on surfaces of elemental ferromagnets. The origin of frustration is the competition of the antiferromagnetic exchange coupling among the Cr or Mn atoms with the antiferromagnetic (for Cr) or ferromagnetic (for Mn) exchange coupling between the impurities and the substrate. We find that Cr and Mn first-neighbouring dimers and a Mn trimer on Ni(001) show non-collinear behavior nearly degenerate with the most stable collinear configuration. Increasing the distance between the dimer atoms leads to a collinear behavior, similar to the one of the single impurities. Finally, we compare some of the non-collinear {\it ab-initio} results to those obtained within a classical Heisenberg model, where the exchange constants are fitted to total energies of the collinear states; the agreement is surprisingly good.

cond-mat.mtrl-sci↗

arXiv2005

Fe clusters on Ni and Cu: size and shape dependence of the spin moment

We present ab-initio calculations of the electronic structure of small Fe clusters (1-9 atoms) on Ni(001), Ni(111), Cu(001) and Cu(111) surfaces. Emphasis is given on the spin moments, and their dependence on cluster size and shape. We derive a simple quantitative rule, which relates the moment of each Fe atom linearly to its coordination number. Thus, for an arbitrary Fe cluster the spin moment of the cluster and of the individual Fe atoms can be readily found if the positions of the atoms are known.

cond-mat.mtrl-sci↗