Papers by Author: Mirosław Kozłowski

Abstract: Chemical ordering kinetics in L10- and B2-ordered AB binary intermetallics was simulated by means of Monte Carlo (MC) technique implemented with vacancy mechanism of atomic migration. While vacancy concentration is usually much lower than the antisite defect concentration in L10-ordered systems, triple defects are generated in particular B2–ordered systems. The latter definitely affects the chemical ordering process and requires that full thermal vacancy thermodynamics is involved in B2-ordering simulations. The study on L10-ordered binaries was dedicated to FePt thin layers considered as a material for ultra-high-density magnetic storage media. Metastability of the L10 c-variant with monoatomic planes parallel to the layer surface and off-plane easy magnetization was revealed. Thermal vacancy formation in B2-ordered binaries was modelled by implementing a mean-field Hamiltonian with a specific formalism of phase equilibria in a latticegas composed of atoms and vacancies. It was demonstrated that for particular pair-interaction energetics, equilibrium concentrations of vacancies and antisites result mutually proportional in well-defined temperature ranges. The MC simulations of B2-ordering kinetics involved the modelled equilibrium vacancy concentration and reproduced the experimentally observed low rate of the process.

Abstract: The L10 ordered MPt(001) thin films (M = Fe or Co) are very interesting for perpendicular recording due to their magnetic anisotropy and magneto-optical behaviours. Epitaxial L10-ordered NiPt(001) / FePt(001) bi-layers were co-deposited on MgO(100) substrates by MBE. The L10 order parameter is high with the concentration modulation along the growth direction. Some FeNiPt2(001) thin films were obtained by interdiffusion of the bilayers. The long-range-order parameter is conserved after interdiffusion (S = 0.75 ± 0.06), which can be explained by different mechanisms: a second-neighbour jump, a six-jump cycle, an anti-structural bridge mechanism or an antisite-pair elimination and creation mechanism, a double vacancy or a triple defect diffusion mechanism. Quenched molecular dynamics calculations in the frame of the second moment approximation of the tight binding method have been performed to obtain the energetic paths of the different mechanisms. The secondneighbour vacancy jump, the simultaneous jumps of bivacancies and the triple defect mechanisms can be ruled out for energetic reasons.

Abstract: “Order-order” relaxations driven by atomic migration in superstructures proceed in nonsteady- state of a system, which relaxes to the equilibrium atomic configuration. Hence, the corresponding studies are complementary to standard steady-state diffusion investigations. Two time scales operating in “order-order” relaxations in L12-ordered (Ni3Al) and L10-ordered (FePd, FePt) binary intermetallics were experimentally observed. On the other hand, in B2-ordered NiAl – known of a giant vacancy concentration, “order-order” relaxations appeared surprisingly slow. Definite relationships between the activation energies for diffusion ( ) D A E and “order-order” relaxations ( ) O O A E − were revealed: ( ) D A E < ( ) O O A E − in L12-type superstructure; ( ) D A E ³ ( ) O O A E − in L10- and in B2-type superstructures. Corresponding simulation studies elucidated the specific atomistic mechanism of the processes. It has been shown that different time scales active in “order-order” relaxations in L12 and L10-ordered systems follow from specific atomic-jump correlations, which result from non-steady-state conditions and particular superlattice geometries: the availability of easy diffusion channels. A model of “order-order” kinetics in NiAl as controlled by a triple-defect mechanism is proposed.