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X. Zhai

Publications and source records attributed to X. Zhai.

6 recordsLinked to original sources

Resonant soft x-ray scattering from La(1-x)Sr(x)MnO(3) quantum wire arrays

We describe a strategy for using resonant soft x-ray scattering (RSXS) to study the electronic structure of transition metal oxide quantum wires. Using electron beam lithography and ion milling, we have produced periodic, patterned arrays of colossal magnetoresistance (CMR) phase La(1-x)Sr(x)MnO(3) consisting of ~ 5000 wires, each of which is 80 nm in width. The scattered intensity exhibits a series of peaks that can be interpreted as Bragg reflections from the periodic structure or, equivalently, diffraction orders from the grating-like structure. RSXS measurements at the Mn L(2,3) edge, which has a large magnetic cross section, show clear evidence for a magnetic superstructure with a commensurate period of five wires, which we interpret as commensurately modulated antiferromagnetism. This superstructure, which is accompanied by non-trivial reorganization of the magnetization within each wire, likely results from classical dipole interactions among the wires. We introduce a simple, exactly soluble, analytic model of the scattering that captures, semi-quantitatively, the primary features in the RSXS data; this model will act as a foundation for forthcoming, detailed studies of the magnetic structure in these systems.

cond-mat.str-el

Magnetically asymmetric interfaces in a (LaMnO$_3$)/(SrMnO$_3$) superlattice due to structural asymmetries

Polarized neutron reflectivity measurements of a ferromagnetic [(LaMnO$_3$)$_{11.8}$/(SrMnO$_3$)$_{4.4}$]$_6$ superlattice reveal a modulated magnetic structure with an enhanced magnetization at the interfaces where LaMnO$_3$ was deposited on SrMnO$_3$ (LMO/SMO). However, the opposite interfaces (SMO/LMO) are found to have a reduced ferromagnetic moment. The magnetic asymmetry arises from the difference in lateral structural roughness of the two interfaces observed via electron microscopy, with strong ferromagnetism present at the interfaces that are atomically smooth over tens of nanometers. This result demonstrates that atomic-scale roughness can destabilize interfacial phases in complex oxide heterostructures.

cond-mat.mtrl-sci

The metal-insulator transition and its relation to magnetic structure in (LaMnO3)2n/(SrMnO3)n superlattices

Superlattices of (LaMnO3)2n/(SrMnO3)n (n=1 to 5), composed of the insulators LaMnO3 and SrMnO3, undergo a metal-insulator transition as a function of n, being metallic for n<=2 and insulating for n>=3. Measurements of transport, magnetization and polarized neutron reflectivity reveal that the ferromagnetism is relatively uniform in the metallic state, and is strongly modulated in the insulating state, being high in LaMnO3 and suppressed in SrMnO3. The modulation is consistent with a Mott transition driven by the proximity between the (LaMnO3)/(SrMnO3) interfaces. Disorder localizes states at the Fermi level at the interfaces for n>=3. We suggest that this disorder is due to magnetic frustration at the interfaces.

cond-mat.str-el

Viscous spin exchange torque on precessional magnetization in $(\mathrm{LaMnO}_3)_{2n}/(\mathrm{SrMnO}_3)_{n}$ superlattices

Photoinduced magnetization dynamics is investigated in chemically ordered $(\mathrm{LaMnO}_3)_{2n}/(\mathrm{SrMnO}_3)_n$ superlattices using the time-resolved magneto-optic Kerr effect. A monotonic frequency-field dependence is observed for the $n=1$ superlattice, indicating a single spin population consistent with a homogeneous hole distribution. In contrast, for $n\geq2$ superlattices, a large precession frequency is observed at low fields indicating the presence of an exchange torque in the dynamic regime. We propose a model that ascribes the emergence of exchange torque to the coupling between two spin populations -- viscous and fast spins.

cond-mat.mtrl-sci

Nanoscale Suppression of Magnetization at Atomically Assembled Manganite Interfaces

Using polarized X-rays, we compare the electronic and magnetic properties of a La(2/3)Sr(1/3)MnO(3)(LSMO)/SrTiO(3)(STO) and a modified LSMO/LaMnO(3)(LMO)/STO interface. Using the technique of X-ray resonant magnetic scattering (XRMS), we can probe the interfaces of complicated layered structures and quantitatively model depth-dependent magnetic profiles as a function of distance from the interface. Comparisons of the average electronic and magnetic properties at the interface are made independently using X-ray absorption spectroscopy (XAS) and X-ray magnetic circular dichroism (XMCD). The XAS and the XMCD demonstrate that the electronic and magnetic structure of the LMO layer at the modified interface is qualitatively equivalent to the underlying LSMO film. From the temperature dependence of the XMCD, it is found that the near surface magnetization for both interfaces falls off faster than the bulk. For all temperatures in the range of 50K - 300K, the magnetic profiles for both systems always show a ferromagnetic component at the interface with a significantly suppressed magnetization that evolves to the bulk value over a length scale of ~1.6 - 2.4 nm. The LSMO/LMO/STO interface shows a larger ferromagnetic (FM) moment than the LSMO/STO interface, however the difference is only substantial at low temperature.

cond-mat.str-el

Suppressed Magnetization at the Surfaces and Interfaces of Ferromagnetic Metallic Manganites

What happens to ferromagnetism at the surfaces and interfaces of manganites? With the competition between charge, spin, and orbital degrees of freedom, it is not surprising that the surface behavior may be profoundly different than that of the bulk. Using a powerful combination of two surface probes, tunneling and polarized x-ray interactions, this paper reviews our work on the nature of the electronic and magnetic states at manganite surfaces and interfaces. The general observation is that ferromagnetism is not the lowest energy state at the surface or interface, which results in a suppression or even loss of ferromagnetic order at the surface. Two cases will be discussed ranging from the surface of the quasi-2D bilayer manganite (La$_{2-2x}$Sr$_{1+2x}$Mn$_2$O$_7$) to the 3D Perovskite (La$_{2/3}$Sr$_{1/3}$MnO$_3$)/SrTiO$_3$ interface. For the bilayer manganite, that is, ferromagnetic and conducting in the bulk, these probes present clear evidence for an intrinsic insulating non-ferromagnetic surface layer atop adjacent subsurface layers that display the full bulk magnetization. This abrupt intrinsic magnetic interface is attributed to the weak inter-bilayer coupling native to these quasi-two-dimensional materials. This is in marked contrast to the non-layered manganite system (La$_{2/3}$Sr$_{1/3}$MnO$_3$/SrTiO$_3$), whose magnetization near the interface is less than half the bulk value at low temperatures and decreases with increasing temperature at a faster rate than the bulk.

cond-mat.str-el