We report magnetization experiments in two magnetically isolated ferromagnetic nanotubes of perovskite La$_{0.67}$Ca$_{0.33}$MnO$_3$. The results show that the magnetic anisotropy is determined by the sample shape although the coercive field is reduced by incoherent magnetization reversal modes. The temperature dependence of the magnetization reveals that the magnetic behavior is dominated by grain surface properties. These measurements were acquired using a Silicon micro-mechanical oscillator working in its resonant mode. The sensitivity was enough to measure the magnetic properties of these two samples with a mass lower than 14 picograms and to obtain for the first time the magnetization loop for one isolated nanotube.
We present a study of interlayer coupling and proximity effects in a La$_{0.66}$Ca$_{0.33}$MnO$_3$(10 nm)/YBa$_2$Cu$_3$O$_7$(10 nm) superlattice. Using element-sensitive x-ray probes, the magnetic state of Mn can be probed without seeing the strong diamagnetism of the superconductor, which makes this approach ideal to study changes in the magnetic properties across the superconducting transition. By a combined experiment using {it in situ} transport measurements during polarized soft x-ray measurements, we were able to see no noticeable influence of the superconducting state on the magnetic properties and no evidence for magnetic coupling across a 10 nm YBCO layer.
We discuss the effects of local structure on the electrical transport and magnetic properties of La(0.67)Ca(0.33)Mn(1-x)Ti(x)O(3) system.Based on the intercomparison of the structure, transport and magnetic properties of the Mn site substituted La(0.67)Ca(0.33)MnO(3) with isovalent diamagnetic and paramagnetic ions, we argue that local structural effects have a decisive role to play, compared to the local spin coupling effects, in the ferromagnetic-metallic ground state of the CMR manganites
Mn $K$-edge fluorescence data are presented for thin film samples (3000~AA) of Colossal Magnetoresistive (CMR) La$_{0.67}$Ca$_{0.33}$MnO$_3$: as-deposited, and post-annealed at 1000 K and 1200 K. The local distortion is analyzed in terms of three contributions: static, phonon, and an extra, temperature-dependent, polaron term. The polaron distortion is very small for the as-deposited sample and increases with the annealing temperature. In contrast, the static distortion in the samples decreases with the annealing temperature. Although the local structure of the as-deposited sample shows very little temperature dependence, the change in resistivity with temperature is the largest of these three thin film samples. The as-deposited sample also has the highest magnetoresistance (MR), which indicates some other mechanism may also contribute to the transport properties of CMR samples. We also discuss the relationship between local distortion and the magnetization of the sample.
In this paper, we examine the possible influence of extrinsic factors on the electrical and magnetotransport of La(0.67)Ca(0.33)Mn(1-x)Ru(x)O(3) (x < 0.10). These results not only exclude the extrinsic factors, but establishes the fact that the metal transitions both exhibiting MR is intrinsic to Ru substituted La(0.67)Ca(0.33)MnO(3) and the system. These results substantiate our hypothesis that Ru substituted system undergoes a magnetic phase separation involving the co-existence of two ferromagnetic-metallic phases in its ground state.
With x-ray absorption spectroscopy we investigated the orbital reconstruction and the induced ferromagnetic moment of the interfacial Cu atoms in YBa$_2$Cu$_3$O$_{7}$/La$_{2/3}$Ca$_{1/3}$MnO$_3$ (YBCO/LCMO) and La$_{2-x}$Sr$_{x}$CuO$_4$/La$_{2/3}$Ca$_{1/3}$MnO$_3$ (LSCO/LCMO) multilayers. We demonstrate that these electronic and magnetic proximity effects are coupled and are common to these cuprate/manganite multilayers. Moreover, we show that they are closely linked to a specific interface termination with a direct Cu-O-Mn bond. We furthermore show that the intrinsic hole doping of the cuprate layers and the local strain due to the lattice mismatch between the cuprate and manganite layers are not of primary importance. These findings underline the central role of the covalent bonding at the cuprate/manganite interface in defining the spin-electronic properties.