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Register a new userInverse photoemission spectroscopic studies on phase separated La$_{0.2}$Sr$_{0.8}$MnO$_{3}$
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We have studied the temperature evolution of the inverse photoemission spectra of phase separated La$_{0.2}$Sr$_{0.8}$MnO$_{3}$. To identify the features in the room temperature experimental spectra, band structure calculations using Korringa-Kohn-Rostoker Greens function method were carried out. We find that the features generated by local moment disorder calculations give a better match with the experimental spectrum. In the insulating phase, we observed unusually an increased intensity at around the Fermi level. This puzzling behaviour is attributed to the shift in the chemical potential towards the conduction band. The present results clearly show the importance of unoccupied electronic states in better understanding of the phase separated systems.
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The structure, morphology, and electrical properties of epitaxial a-axis oriented thin films of Nd(0.2)Sr(0.8)MnO(3) are reported for thicknesses 10 nm <= t <= 150 nm. Films were grown with both tensile and compressive strain on various substrates. It is found that the elongated crystallographic c-axes of the films remain fully strained to the substrates for all thicknesses in both strain states. Relaxation of the a and b axes is observed for t>= 65 nm with films grown under tensile strain developing uniaxial crack arrays (running along the c axis) due to a highly anisotropic thermal expansion. For the latter films, the room-temperature in-plane electrical resistivity anisotropy, rho_b/rho_c, increases approximately exponentially with increasing film thickness to values of ~1000 in the thickest films studied. Films under tension have their Neel temperatures enhanced by ~25 K independent of thickness, consistent with an enhancement of ferromagnetic exchange along their expanded c axes.
The many surface reconstructions of (110)-oriented lanthanum--strontium manganite (La$_{0.8}$Sr$_{0.2}$MnO$_3$, LSMO) were followed as a function of the oxygen chemical potential ($mu_text{O}$) and the surface cation composition. Decreasing $mu_text{O}$ causes Mn to migrate across the surface, enforcing phase separation into A-site-rich areas and a variety of composition-related, structurally diverse B-site-rich reconstructions. The composition of these phase-separated structures was quantified with scanning tunneling microscopy (STM), and these results were used to build a 2D phase diagram of the LSMO(110) equilibrium surface structures.
The ferromagnetic and insulating state observed in La$_{1-x}$Ca$_{x}$MnO$_3$, 0.125$<$x$<$0.2, is characterized by structural and magnetic anomalies below T$_C$, similar to those observed in the x$_{Sr}$$approx$1/8. A neutron scattering study of the superlattice {bf Q$_0$}= (0,0,1+/4)$_{cub}$ peak, and of the magnetic excitations are reported in the x$_{Ca}$=0.2 sample. The occurrence of this superstructure is associated with the observation of a gap in the spin dynamics, at a {bf q$_0$} wave-vector ({bf q$_0$}={bf Q$_0$}-$tau$) with the same modulus $|${bf q$_0$}$|$ in all directions, which divides the dispersion into two regimes. For $|${bf q}$|$$<$$|${bf q$_0$}$|$ the dispersion is splitted into two or three curves. For $|${bf q}$|$$>$$|${bf q$_0$}$|$, magnetic excitations lock on acoustic and optic phonon energies, revealing a new kind of magneto-vibrational coupling. We suggest an analysis in terms of two distinct magnetic couplings, associated with two ferromagnetic media involved into a collective state.
We have studied a non volatile memory effect in the mixed valent compound La$_{0.5}$Ca$_{0.5}$MnO$_{3}$ induced by magnetic field (H). In a previous work [R.S. Freitas et al., Phys. Rev. B 65 (2002) 104403], it has been shown that the response of this system upon application of H strongly depends on the temperature range, related to three well differentiated regimes of phase separation occurring below 220 K. In this work we compare memory capabilities of the compound, determined following two different experimental procedures for applying H, namely zero field cooling and field cooling the sample. These results are analyzed and discussed within the scenario of phase separation.
Polycrystalline La$_{2/3}$Sr$_{1/3}$MnO$_{3}$ (LSMO) thin films were synthesized by pulsed laser ablation on single crystal (100) yttria-stabilized zirconia (YSZ) substrates to investigate the mechanism of magneto-transport in a granular manganite. Different degrees of granularity is achieved by using the deposition temperature (T$_{D}$) of 700 and 800 $^{0}$C. Although no significant change in magnetic order temperature (T$_C$) and saturation magnetization is seen for these two types of films, the temperature and magnetic field dependence of their resistivity ($rho$(T, H)) is strikingly dissimilar. While the $rho$(T,H) of the 800 $^{0}$C film is comparable to that of epitaxial samples, the lower growth temperature leads to a material which undergoes insulator-to-metal transition at a temperature (T$_{P}$ $approx$ 170 K) much lower than T$_C$. At T $ll$ T$_P$, the resistivity is characterized by a minimum followed by ln $emph{T}$ divergence at still lower temperatures. The high negative magnetoresistance ($approx$ 20$%$) and ln $emph{T}$ dependence below the minimum are explained on the basis of Kondo-type scattering from blocked Mn-spins in the intergranular material. Further, a striking feature of the T$_D$ = 700 $^{0}$C film is its two orders of magnitude larger anisotropic magnetoresistance (AMR) as compared to the AMR of epitaxial films. We attribute it to unquenching of the orbital angular momentum of 3d electrons of Mn ions in the intergranular region where crystal field is poorly defined.
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