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Register a new userX-ray method to study temperature-dependent stripe domains in MnAs/GaAs(001)
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Added by
Harry Westfahl Junior
Publication date
2004
fields
Physics
and research's language is
English
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MnAs films grown on GaAs (001) exhibit a progressive transition between hexagonal (ferromagnetic) and orthorhombic (paramagnetic) phases at wide temperature range instead of abrupt transition during the first-order phase transition. The coexistence of two phases is favored by the anisotropic strain arising from the constraint on the MnAs films imposed by the substrate. This phase coexistence occurs in ordered arrangement alternating periodic terrace steps. We present here a method to study the surface morphology throughout this transition by means of specular and diffuse scattering of soft x-rays, tuning the photon energy at the Mn 2p resonance. The results show the long-range arrangement of the periodic stripe-like structure during the phase coexistence and its period remains constant, in agreement with previous results using other techniques.
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We demonstrate a scheme for optically patterning nuclear spin polarization in semiconductor/ferromagnet heterostructures. A scanning time-resolved Kerr rotation microscope is used to image the nuclear spin polarization that results when GaAs/MnAs epilayers are illuminated with a focused laser having a Gaussian profile. Rather than tracking the intensity profile of the laser spot, these images reveal that the nuclear polarization forms an annular lateral structure having circular symmetry with a dip rather than a peak at its center.
We have studied the electronic structure of hexagonal MnAs, as epitaxial continuous film on GaAs(001) and as nanocrystals embedded in GaAs, by Mn 2p core-level photoemission spectroscopy. Configuration-interaction analyses based on a cluster model show that the ground state of the embedded MnAs nanocrystals is dominated by a d5 configuration that maximizes the local Mn moment. Nanoscaling and strain significantly alter the properties of MnAs. Internal strain in the nanocrystals results in reduced p-d hybridization and enhanced ionic character of the Mn-As bonding interactions. The spatial confinement and reduced p-d hybridization in the nanocrystals lead to enhanced d-electron localization, triggering d-d electron correlations and enhancing local Mn moments. These changes in the electronic structure of MnAs have an advantageous effect on the Curie temperature of the nanocrystals, which is measured to be remarkably higher than that of bulk MnAs.
We have performed a depth profile study of thermally diffused Mn/GaAs (001) interfaces using photoemission spectroscopy combined with Ar$^+$-ion sputtering. We found that Mn ion was thermally diffused into the deep region of the GaAs substrate and completely reacted with GaAs. In the deep region, the Mn 2$p$ core-level and Mn 3$d$ valence-band spectra of the Mn/GaAs (001) sample heated to 600 $^{circ}$C were similar to those of Ga$_{1-x}$Mn$_x$As, zinc-blende-type MnAs dots, and/or interstitial Mn in tetrahedrally coordinated by As atoms, suggesting that the Mn 3$d$ states were essentially localized but were hybridized with the electronic states of the host GaAs. Ferromagnetism was observed in the dilute Mn phase.
The use of current-generated spin-orbit torques[1] to drive magnetization dynamics is under investigation to enable a new generation of non-volatile, low-power magnetic memory. Previous research has focused on spin-orbit torques generated by heavy metals[2-8], interfaces with strong Rashba interactions[9,10] and topological insulators [11-14]. These families of materials can all be well-described using models with noninteracting-electron bandstructures. Here, we show that electronic interactions within a strongly correlated heavy fermion material, the Kondo lattice system YbAl$_{3}$, can provide a large enhancement in spin-orbit torque. The spin-torque conductivity increases by approximately a factor of 4.5 as a function of decreasing temperature from room temperature to the coherence temperature of YbAl$_{3}$ ($T^* approx 37$ K), with a saturation at lower temperatures, achieving a maximum value greater than any heavy metal element. This temperature dependence mimics the increase and saturation at $T^*$ of the density of states at the Fermi level arising from the ytterbium 4$f$-derived heavy bands in the Kondo regime, as measured by angle-resolved photoemission spectroscopy[15]. We therefore identify the many-body Kondo resonance as the source of the large enhancement of spin-orbit torque in YbAl$_{3}$. Our observation reveals new opportunities in spin-orbit torque manipulation of magnetic memories by engineering quantum many-body states.
In underdoped cuprate superconductors, a rich competition occurs between superconductivity and charge density wave (CDW) order. Whether rotational symmetry breaking (nematicity) occurs intrinsically and generically or as a consequence of other orders is under debate. Here we employ resonant x-ray scattering in stripe-ordered (La,M)_2CuO_4 to probe the relationship between electronic nematicity of the Cu 3d orbitals, structure of the (La,M)_2O_2 layers, and CDW order. We find distinct temperature dependences for the structure of the (La,M)_2O_2 layers and the electronic nematicity of the CuO_2 planes, with only the latter being enhanced by the onset of CDW order. These results identify electronic nematicity as an order parameter that is distinct from a purely structural order parameter in underdoped striped cuprates.
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