A mu SR study of the spin dynamics in Ir-diluted layered manganites

PHYSICA B 326:1-4 (2003) 513-517

Authors:

CA Steer, SJ Blundell, AI Coldea, IM Marshall, T Lancaster, PD Battle, D Gallon, AJ Fargus, MJ Rosseinsky

Abstract:

Dilution on the B-site with Ir or Rh can lead to the enhancement of ferromagnetic couplings in layered manganites. We report a muSR study of the spin dynamics of the layered manganites La0.25Sr1.75MnpIr1-pO4 (p = 0.5, 0.75) as a function of the dilution. We have characterized the static magnetic behavior using SQUID magnetic measurements and used muon spin relaxation spectroscopy to provide evidence for short-range ferromagnetic correlations. Furthermore, the effect of dilution on the critical dynamics in this two-dimensional spin system is reported and related to the dynamics above and below the critical percolation threshold. (C) 2002 Elsevier Science B.V. All rights reserved.

Changes of the spin dynamics in perovskite and bilayer manganite

PHYSICA B 326:1-4 (2003) 500-504

Authors:

AI Coldea, SJ Blundell, CA Steer, FL Pratt, D Prabhakaran, JF Mitchell

Abstract:

We report a series of muSR measurements performed on single crystals of La1-x,SrxMnO3, (0 less than or equal to x less than or equal to 0.125) and on a polycrystalline bilayer manganite La2-2x Sr1+2xMn2O7 (v = 0.52). We find that the temperature dependence of the spinlattice relaxation rate is strongl, dependent on the hole doping and the associated changes in the magnetic structure. Y The systems have competing, anisotropic interactions, leading to a complex interplay of charge, spin and orbital order. This has a significant influence on the spin dynamics, both for perovskite and layered manganites. (C) 2002 Elsevier Science B.V. All rights reserved.

Synthesis and characterization of Ru-doped n = 1 and n = 2 Ruddlesden-Popper manganates

Chemistry of Materials 14:9 (2002) 3976-3983

Authors:

DJ Gallon, PD Battle, SJ Blundell, JC Burley, AI Coldea, EJ Cussen, MJ Rosseinsky, C Steer

Abstract:

Polycrystalline samples of Sr3MnRuO7 and Sr2Mn0.5Ru0.5O4 have been synthesized and characterized by neutron diffraction, dc magnetometry, and magnetotransport measurements. They are, respectively, n = 2 and n = 1 members of the Ruddlesden-Popper (RP) An+1BnO3n+1 family; both have tetragonal (I4/mmm) symmetry and a disordered distribution of Ru and Mn over the six-coordinate sites within the perovskite layers of the RP structure. Neither compound shows long-range magnetic order at 2 K, but a spin-glass transition is observed at 16 K (n = 1) or 25 K (n = 2). In the case of the n = 2 compound only, the magnetic transition is accompanied by a reduction in the zero-field electrical conductivity. A maximum magnetoresistance of ∼8% in 14 T is found in both compounds.

Growth of large La1-xSrxMnO3 single crystals under argon pressure by the floating-zone technique

J CRYST GROWTH 237 (2002) 806-809

Authors:

D Prabhakaran, AI Coldea, AT Boothroyd, S Blundell

Abstract:

We report the growth of single crystals of La1-xSrxMnO3 (x = 0.0-0.3) by the floating-zone technique in an image furnace under high argon pressure (6-8 atm). Ail excess of Mn in the polycrystalline starting material was used to compensate for the evaporation during growth. single crystals of diameter 8 mm and length 70 mm have been obtained. The phase purity, composition and quality of the crystals were analysed by X-ray diffraction and electron probe microanalysis. We discuss the effect on the crystal growth of varying the amount of Mn excess and of the composition of the growth atmosphere. We also present magnetization and resistivity data for a few of the samples. (C) 2002 Elsevier Science B.V. All rights reserved.

Spin, charge, and orbital ordering in the B-site diluted manganates La2-xSrxGaMnO6

Chemistry of Materials 14:1 (2002) 425-434

Authors:

PD Battle, SJ Blundell, JB Claridge, AI Coldea, EJ Cussen, LD Noailles, MJ Rosseinsky, J Singleton, J Sloan

Abstract:

Oxidation of the ferromagnetic B-site diluted manganese(III) perovskite La2GaMnO6 is investigated by synthesis of the La2-xSrxGaMnO6 series. At the x = 0.3 composition, which corresponds to diamagnetic element substitution at the B-site of metallic LaO.7SrO.3MnO3, the MnIII and MnIV valences order in real space at low temperature with an unusual lamellar motif. Orbital ordering at the MnIII centers in this array maintains ferromagnetism and enhances the static coherent Jahn-Teller distortion over that found for the pure MnIII end-member, facilitating eg electron hopping in the insulating state. Further oxidation to x = 0.5 completely suppresses the charge and orbital ordering, leading to glassy rather than long-range ordered magnetism.