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Register a new userDetermining surface magnetization and local magnetic moments with atomic scale resolution
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We propose a method to determine the direction of surface magnetization and local magnetic moments on the atomic scale. The method comprises high resolution scanning tunneling microscope experiments in conjunction with first principles simulations of the tunneling current. The potential of the method is demonstrated on a model system, antiferromagnetic Mn overlayers on W(110). We expect that it will ultimately allow to study the detailed changes of magnetic surface structures in the vicinity of dopants or impurities.
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B20-type compounds, such as MnSi and FeGe, host helimagnetic and skyrmion phases at the mesoscale, which are canonically explained by the combination of ferromagnetic isotropic interactions with weaker chiral Dzyaloshinskii-Moriya ones. Mysteriously, MnGe evades this paradigm as it displays a noncollinear magnetic state at a much shorter nanometer scale. Here we show that the length scale and volume-dependent magnetic properties of MnGe stem from purely isotropic exchange interactions, generally obtained in the paramagnetic state. Our approach is validated by comparing MnGe with the canonical B20-helimagnet FeGe. The free energy of MnGe is calculated, from which we show how triple-q magnetic states can stabilize by adding higher-order interactions.
Significant progress has been made in spatial resolution using environmental transmission electron microscopes (ETEM), which now enables atomic resolution visualization of structural transformation under variable temperature and gas environments close to materials real operational conditions. Structural transformations are observed by recording images or diffraction patterns at various time intervals using a video camera or by taking snap shots using electron pulses. While time resolution at 15 ns has been reported using pulsed electron beams, the time interval that can be recorded by this technique is currently very limited. For longer recording, however, time resolution inside ETEM has been limited by electron cameras to ~1/30 seconds for a long time. Using the recently developed direct electron detection technology, we have significantly improved the time resolution of ETEM to 2.5 ms (milliseconds) for full frame or 0.625 ms for 0.25 frames.
We report an interesting magnetic behavior of a Co film (thickness ~ 350 {AA}) grown on Si/Ti/Cu buffer layer by electro-deposition (ED) technique. Using depth sensitive X-ray reflectivity and polarized neutron reflectivity (PNR) we observed two layer structures for the Co film grown by ED with a surface layer (thickness ~ 100 {AA}) of reduced density (~ 68% of bulk) compared to rest of the Co film (thickness ~ 250 {AA}). The two layer structure is consistent with the histogram profile obtained from atomic force microscope (AFM) of the film. Interestingly, using PNR, we found that the magnetization in the surface Co layer is inversely (antiferomagnetically) coupled (negative magnetization for surface Co layer) with the rest of the Co layer for the ED grown film. While we compare PNR result for a Co film of similar layered structure grown by sputtering, the film showed a uniform magnetization as expected. We also show that the depth dependent unusual magnetic behavior of ED grown Co film may be responsible for anomalous anisotropic magnetoresistance observed in low field in this film as compared to the Co film grown by sputtering. Combining X-ray scattering, AFM, superconducting quantum interface device magnetometry (SQUID), PNR and magneto-transport measurements we attempted to correlate and compare the structural, magnetic and morphological properties with magneto-transport of Co films grown by ED and sputtering. The study indicates that the interesting surface magnetic property and magneto-transport property of the ED film is caused by its unique surface morphology.
We introduce a massively parallel replica-exchange grand-canonical sampling algorithm to simulate materials at realistic conditions, in particular surfaces and clusters in reactive atmospheres. Its purpose is to determine in an automated fashion equilibrium phase diagrams for a given potential-energy surface (PES) and for any observable sampled in the grand-canonical ensemble. The approach enables an unbiased sampling of the phase space and is embarrassingly parallel. It is demonstrated for a model of Lennard-Jones system describing a surface in contact with a gas phase. Furthermore, the algorithm is applied to Si$_M$ clusters ($M=2, 4$) in contact with an H$_{2}$ atmosphere, with all interactions described at the textit{ab initio} level, i.e., via density-functional theory, with the PBE gradient-corrected exchange-correlation functional. We identify the most thermodynamically stable phases at finite $T, p$(H$_{2}$) conditions.
Atomic vibrations control all thermally activated processes in materials including diffusion, heat transport, phase transformations, and surface chemistry. Recent developments in monochromated, aberration-corrected scanning transmission electron microscopy (STEM) have enabled nanoscale probing of vibrational modes using a focused electron beam. However, to date, no experimental atomic resolution vibrational spectroscopy has been reported. Here we demonstrate atomic resolution by exploiting localized impact excitations of vibrational modes in materials. We show that the impact signal yields high spatial resolution in both covalent and ionic materials, and atomic resolution is available from both optical and acoustic vibrational modes. We achieve a spatial resolution of better than 2 {AA} which is an order of magnitude improvement compared to previous work. Our approach represents an important technical advance that can be used to provide new insights into the relationship between the thermal, elastic and kinetic properties of materials and atomic structural heterogeneities.
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