Tolerance of topological surface states towards magnetic moments: Fe on Bi2Te3 and Bi2Se3

Topological insulators(1-8) are a novel form of matter which features metallic surface states with quasirelativistic dispersion similar to graphene(9). Unlike graphene, the locking of spin and momentum and the protection by time-reversal symmetry(1-8) open up tremendous additional possibilities for external control of transport properties(10-18). Here we show by angle-resolved photoelectron spectroscopy that the topological sur-face states of Bi2Te3 and Bi2Se3 are stable against the deposition of Fe without opening a band gap. This stability extends to low submonolayer coverages meaning that the band gap reported recently(19) for Fe on Bi2Se3 is incorrect as well as to complete monolayers meaning that topological surface states can very well exist at interfaces with ferromagnets in future devices.Comment: 10 pages, 3 figures, submitted to Nature Physics 22. July 201

Reversal of the circular dichroism in the angle-resolved photoemission from Bi2Te3

The helical Dirac fermions at the surface of topological insulators show a strong circular dichroism which has been explained as being due to either the initial-state spin angular momentum, the initial-state orbital angular momentum, or the handedness of the experimental setup. All of these interpretations conflict with our data from Bi2Te3 which depend on the photon energy and show several sign changes. Our one-step photoemission calculations coupled to ab initio theory confirm the sign change and assign the dichroism to a final-state effect. The spin polarization of the photoelectrons, instead, remains a reliable probe for the spin in the initial state.Comment: 16 pages, 4 figures; submitted to Physical Review Letter

Quasi free-standing one-dimensional nanocrystals of PbTe grown in 1.4 nm SWNTs

Here, we show successful filling of 1.4 nm single-walled carbon nanotubes (SWNT) with PbTe nanocrystals. The structure of one-dimensional PbTe in SWNT was determined using high-resolution transmission electron microscopy (HRTEM). The electronic structure of composites was studied by optical absorbance and Raman spectroscopies indicating no noticeable interaction of encapsulated PbTe with SWNT wall. Experimental data are supported by ab-initio calculations, showing non-zero density of states at the Fermi level of PbTe@SWNT(10,10) provided by both SWNT and PbTe states and thus metallic conductivity of the composite

Impact of ordering on the reactivity of mixed crystals of topological insulators with anion substitution Bi2SeTe2 and Sb2SeTe2

Three dimensional topological insulators TIs are exotic materials with unique properties. Tetradymite type binary chalcogenides of bismuth and antimony, as well as their mixed crystals, belong to prototypical TIs. Potential device applications of these materials require in depth knowledge of their stability in the ambient atmosphere and other media maintained during their processing. Here we investigated the reactivity of mixed crystals with anion substitution, Bi2 Se1 xTex 3 and Sb2 Se1 xTex 3, towards molecular oxygen using both in situ and ex situ X ray photoelectron spectroscopy. The results indicate that, in contrast to cation substitution, partial substitution of tellurium by selenium atoms leads to anomalously high surface reactivity, which even exceeds that of the most reactive binary constituent. We attribute this effect to anion ordering that essentially modifies the bond geometry, especially the respective bond angles as modeled by DF

Native and graphene-coated flat and stepped surfaces of TiC

Titanium carbide attracts growing interest as a substrate for graphene growth and as a component of the composite carbon materials for supercapacitors, an electrode material for metal-air batteries. For all these applications, the surface chemistry of titanium carbide is highly relevant and being, however, insufficiently explored especially at atomic level is a subject of our studies. Applying X-ray photoelectron spectroscopy (XPS) to clean (111) and (755) surfaces of TiC, we were able to obtain the detailed spectroscopic pattern containing information on the plasmon structure, shake up satellite, the peak asymmetry and, finally, surface core level shift (SCLS) in C 1s spectra. The latter is essential for further precise studies of chemical reactions. Later on, we studied interface between TiC (111) and (755) and graphene and found the SCLS variation due to strong chemical interaction between graphene and substrate. This interaction is also reflected in the peculiar band structure of graphene probed by angle-resolved photoelectron spectroscopy (ARPES). Based on LEED data the structure is close to (7√3 × 7√3)R30°, with graphene being slightly corrugated. We found that similarly to the graphene on metals, the chemical interaction between graphene and TiC can be weakened by means of intercalation of oxygen atoms underneath graphene.We thank Helmholtz-Zentrum Berlin (HZB) for the allocation of synchrotron radiation beamtimes at the Russian-German and UE112-PGM2 beamlines. The work was financially supported by the Russian Science Foundation (project 16-42-01093). DFT calculations were performed at “Lomonosov” MSU supercomputer.Peer reviewe

Intact Dirac cone of Bi2Te3 covered with a monolayer Fe

The topological surface state of Bi2Te3 leads to high photoemisson intensity from its Dirac point. This allows us to investigate the effect of larger amounts of deposited Fe than previously achieved for Bi2Se3. The Dirac point is shown to stay intact up to at least a monolayer showing the robustness of the topological state towards disordered magnetic moment

Mechanistic Studies of Gas Reactions with Multicomponent Solids What Can We Learn By Combining NAP XPS and Atomic Resolution STEM EDX?

Rapid development of experimental techniques has enabled real time studies of solid–gas reactions at the level reaching the atomic scale. In the present paper, we focus on a combination of atomic resolution STEM/EDX, which visualizes the reaction zone, and near ambient pressure (NAP) XPS, which collects information for a surface layer of variable thickness under reaction conditions. We compare the behavior of two affined topological insulators, Bi2Te3 and Sb2Te3. We used a simple reaction with molecular oxygen occurring at 298 K, which is of practical importance to avoid material degradation. Despite certain limitations, a combination of in situ XPS and ex situ cross-sectional STEM/EDX allowed us to obtain a self-consistent picture of the solid–gas reaction mechanism for oxidation of Sb2Te3 and Bi2Te3 crystals, which includes component redistribution between the oxide and the subsurface layer and Te segregation with formation of a thin ordered layer at the interface. The process is multistep in case of both compounds. At the very beginning of the oxidation process the reactivity is determined by the energy benefit of the corresponding element–oxygen bond formation. Further in the oxidation process, the behavior of these two compounds becomes similar and features component redistribution between the oxide and the subsurface layer

The impact of dimensionality and stoichiometry of CuBr on its coupling to sp(2)-carbon

A possible coupling of one-dimensional crystal to their template material plays crucial role when its electronic structure is evaluated. Here a comparative study of the interaction between CuBr and sp(2)-carbon in 1D and 2D structures as probed by X-ray absorption, photoemission and DFT calculations is reported. The 1D system, i.e. a non-stoichiometric CuBr crystal embedded into a single-walled carbon nanotube (CuBr@SWNT) revealed notable hybridization in contrast to a CuBr film deposited on graphene or graphite. CuBr is coupled to the nanotube due to its low dimensionality and strong coordination deficiency of atoms thus forming one-dimensional nanocrystal, which is non-free-standing. (C) 2015 Elsevier Ltd. All rights reserved