Searcharxiv⌕ Search

arXiv subjects

Jens Wiebe

Publications and source records attributed to Jens Wiebe.

At least 37 records · Page 2Linked to original sources

Spin-polarized Yu-Shiba-Rusinov states in an iron based superconductor

Yu-Shiba-Rusinov (YSR) bound states appear when a magnetic atom interacts with a superconductor. Here, we report on spin-resolved spectroscopic studies of YSR states related with Fe atoms deposited on the surface of the topological superconductor FeTe0.55Se0.45 using a spin-polarized scanning tunneling microscope. We clearly identify the spin signature of pairs of YSR bound states at finite energies within the superconducting gap having opposite spin polarization as theoretically predicted. In addition, we also observe zero-energy bound states for some of the adsorbed Fe atoms. In this case, a spin signature is found to be absent indicating the absence of Majorana bound states associated with Fe adatoms on FeTe0.55Se0.45.

cond-mat.supr-con↗

Spin-orbit coupling induced splitting of Yu-Shiba-Rusinov states in antiferromagnetic dimers

Magnetic atoms coupled to the Cooper pairs of a superconductor induce Yu-Shiba-Rusinov states (in short Shiba states). In the presence of sufficiently strong spin-orbit coupling, the bands formed by hybridization of the Shiba states in ensembles of such atoms can support low-dimensional topological superconductivity with Majorana bound states localized on the ensembles' edges. Yet, the role of spin-orbit coupling for the hybridization of Shiba states in dimers of magnetic atoms, the building blocks for such systems, is largely unexplored. Here, we reveal the evolution of hybridized multi-orbital Shiba states from a single Mn adatom to artificially constructed ferromagnetically and antiferromagnetically coupled Mn dimers placed on a Nb(110) surface. Upon dimer formation, the atomic Shiba orbitals split for both types of magnetic alignment. Our theoretical calculations attribute the unexpected splitting in antiferromagnetic dimers to spin-orbit coupling and broken inversion symmetry at the surface. Our observations point out the relevance of previously unconsidered factors on the formation of Shiba bands and their topological classification.

cond-mat.supr-con↗

Atomic-scale spin-polarization maps using functionalized superconducting probes

A scanning tunneling microscope (STM) with a magnetic tip that has a sufficiently strong spin-polarization can be used to map the sample's spin structure down to the atomic scale but usually lacks the possibility to absolutely determine the value of the sample's spin-polarization. Magnetic impurities in superconducting materials give rise to pairs of perfectly, i.e. 100% spin-polarized sub-gap resonances. In this work, we functionalize the apex of a superconducting Nb STM-tip with such impurity states by attaching Fe atoms to probe the spin-polarization of atom-manipulated Mn nanomagnets on a Nb(110) surface. By comparison with spin-polarized STM measurements of the same nanomagnets using Cr bulk tips we demonstrate an extraordinary spin-sensitivity and the possibility to measure the sample's spin-polarization values quantitatively with our new functionalized probes.

cond-mat.supr-con↗

Controlling in-gap end states by linking nonmagnetic atoms and artificially-constructed spin chains on superconductors

Chains of magnetic atoms with either strong spin-orbit coupling or spiral magnetic order which are proximity-coupled to superconducting substrates can host topologically non-trivial Majorana bound states. The experimental signature of these states consists of spectral weight at the Fermi energy and spatially localized near the ends of the chain. However, topologically trivial Yu-Shiba-Rusinov in-gap states localized near the ends of the chain can lead to similar spectra. Here, we explore a protocol to disentangle these contributions by artificially augmenting a candidate Majorana spin chain with orbitally-compatible nonmagnetic atoms. Combining scanning tunneling spectroscopy with ab-initio and tight-binding calculations, we realize a sharp spatial transition between the proximity-coupled spiral magnetic order and the non-magnetic superconducting wire termination, with persistent zero-energy spectral weight localized at either end of the magnetic spiral. Our findings open a new path towards the control of the spatial position of in-gap end states, trivial or Majorana, via different chain terminations, and the realization of designer Majorana chain networks for demonstrating topological quantum computation.

cond-mat.supr-con↗

Colloquium: Atomic spin chains on surfaces

In the present Colloquium, we focus on the properties of 1-D magnetic systems on solid surfaces. From the emulation of 1-D quantum phases to the potential realization of Majorana edge states, spin chains are unique systems to study. The advent of scanning tunnelling microscope (STM) based techniques has permitted us to engineer spin chains in an atom-by-atom fashion via atom manipulation and to access their spin states on the ultimate atomic scale. Here, we present the current state of research on spin correlations and dynamics of atomic spin chains as studied by the STM. After a brief review of the main properties of spin chains on solid surfaces, we classify spin chains according to the coupling of their magnetic moments with the holding substrate. This classification scheme takes into account that the nature and lifetimes of the spin-chain excitation intrinsically depend on the holding substrate. We first show the interest of using insulating layers on metals, which generally results in an increase in the spin state's lifetimes such that their quantized nature gets evident and they are individually accessible. Next, we show that the use of semiconductor substrates promises additional control through the tunable electron density via doping. When the coupling to the substrate is increased for spin chains on metals, the substrate conduction electron mediated interactions can lead to emergent exotic phases of the coupled spin chain-substrate conduction electron system. A particularly interesting example is furnished by superconductors. Magnetic impurities induce states in the superconducting gap. Due to the extended nature of the spin chain, the in-gap states develop into bands that can lead to the emergence of 1-D topological superconductivity and, consequently to the appearance of Majorana edge states.

cond-mat.mes-hall↗

Magnetism and in-gap states of 3d transition metal atoms on superconducting Re

Magnetic atoms on heavy-element superconducting substrates are potential building blocks for realizing topological superconductivity in one- and two-dimensional atomic arrays. Their localized magnetic moments induce so-called Yu-Shiba-Rusinov (YSR) states inside the energy gap of the substrate. In the dilute limit, where the electronic states of the array atoms are only weakly coupled, proximity of the YSR states to the Fermi energy is essential for the formation of topological superconductivity in the band of YSR states. Here, we reveal via scanning tunnel spectroscopy and ab initio calculations of a series of 3d transition metal atoms (Mn, Fe, Co) adsorbed on the heavy-element superconductor Re that the increase of the Kondo coupling and sign change in magnetic anisotropy with d-state filling is accompanied by a shift of the YSR states through the energy gap of the substrate and a crossing of the Fermi level. The uncovered systematic trends enable the identification of the most promising candidates for the realization of topological superconductivity in arrays of similar systems.

cond-mat.supr-con↗

Stabilizing spin systems via symmetrically tailored RKKY interactions

The spin of a single atom adsorbed on a substrate is a promising building block for future spintronics and quantum computation schemes. To process spin information and also for increased magnetic stability, these building blocks have to be coupled. For a single atom, a high symmetry of the environment is known to lead to increased spin stability. However, little is known about the role of the nature and symmetry of the magnetic couplings. Here, we study arrays of atomic spins coupled via the ubiquitous Ruderman-Kittel-Kasuya-Yosida (RKKY) interaction, focusing on its two anisotropic parts: the Dzyaloshinskii-Moriya (DM) and the symmetric anisotropic exchange interactions. First, we show that the high spin stability of an iron trimer can be remotely detected by a nearby iron atom, and how the DM interaction can lead to its destabilization. Second, we find that adding more nearby iron atoms almost always leads to a destabilization of the trimer, due to a non-local effective transverse anisotropy originating in the symmetric anisotropic exchange interaction. This transverse anisotropy can be quenched only for highly symmetric structures, for which the spin lifetime of the array is increased by orders of magnitude.

cond-mat.mes-hall↗

Engineering the spin couplings in atomically crafted spin chains on an elemental superconductor

Magnetic atoms on a superconductor give rise to Yu-Shiba-Rusinov (YSR) states within the superconducting energy gap. A spin chain of magnetic adatoms on an s-wave superconductor may lead to topological superconductivity accompanied by the emergence of Majorana modes at the chain ends. For their usage in quantum computation, it is a prerequisite to artificially assemble the chains and control the exchange couplings between the spins in the chain and in the substrate. Here, using a scanning tunneling microscope tip, we demonstrate engineering of the energy levels of the YSR states by placing interstitial Fe atoms in close proximity to adsorbed Fe atoms on an oxidized Ta surface. Based on this prototype platform, we show that the interaction within a long chain can be strengthened by linking the adsorbed Fe atoms with the interstitial ones. Our work adds an important step towards the controlled design and manipulation of Majorana end states.

cond-mat.supr-con↗

Non-collinear spin states in bottom-up fabricated atomic chains

Non-collinear spin states with unique rotational sense, such as chiral spin-spirals, are recently heavily investigated because of advantages for future applications in spintronics and information technology and as potential hosts for Majorana Fermions when coupled to a superconductor. Tuning the properties of such spin states, e.g., the rotational period and sense, is a highly desirable yet difficult task. Here, we experimentally demonstrate the bottom-up assembly of a spin-spiral derived from a chain of Fe atoms on a Pt substrate using the magnetic tip of a scanning tunneling microscope as a tool. We show that the spin-spiral is induced by the interplay of the Heisenberg and Dzyaloshinskii-Moriya components of the Ruderman-Kittel-Kasuya-Yosida interaction between the Fe atoms. The relative strengths and signs of these two components can be adjusted by the interatomic Fe distance, which enables tailoring of the rotational period and sense of the spin-spiral.

cond-mat.mes-hall↗

Long spin relaxation times in a transition metal atom in direct contact to a metal substrate

Long spin relaxation times are a prerequisite for the use of spins in data storage or nanospintronics technologies. An atomic-scale solid-state realization of such a system is the spin of a transition metal atom adsorbed on a suitable substrate. For the case of a metallic substrate, which enables directly addressing the spin by conduction electrons, the experimentally measured lifetimes reported to date are on the order of only hundreds of femtoseconds. Here, we show that the spin states of iron atoms adsorbed directly on a conductive platinum substrate have an astonishingly long spin relaxation time in the nanosecond regime, which is comparable to that of a transition metal atom decoupled from the substrate electrons by a thin decoupling layer. The combination of long spin relaxation times and strong coupling to conduction electrons implies the possibility to use flexible coupling schemes in order to process the spin-information.

cond-mat.mes-hall↗

Domain imaging across the magneto-structural phase transition in Fe$_{1+y}$Te

The investigation of the magnetic phase transitions in the parent compounds of Fe-based superconductors is regarded essential for an understanding of the pairing mechanism in the related superconducting compounds. Even though the chemical and electronic properties of these materials are often strongly inhomogeneous on a nanometer length scale, studies of the magnetic phase transitions using spatially resolved experimental techniques are still scarce. Here, we present a real space spin-resolved scanning tunneling microscopy investigation of the surface of Fe$_{1+y}$Te single crystals with different excess Fe content, $y$, which are continuously driven through the magnetic phase transition. For Fe$_{1.08}$Te, the transition into the low-temperature monoclinic commensurate antiferromagnetic phase is accompanied by the sudden emergence of ordering into four rotational domains with different orientations of the monoclinic lattice and of the antiferromagnetic order, showing how structural and magnetic order are intertwined. In the low-temperature phase of Fe$_{1.12}$Te one type of the domain boundaries disappears, and the transition into the paramagnetic phase gets rather broad, which is assigned to the formation of a mixture of orthorhombic and monoclinic phases.

cond-mat.supr-con↗

Enhanced spin ordering temperature in ultrathin FeTe films grown on a topological insulator

We studied the temperature dependence of the diagonal double-stripe spin order in one and two unit cell thick layers of FeTe grown on the topological insulator Bi_2Te_3 via spin-polarized scanning tunneling microscopy. The spin order persists up to temperatures which are higher than the transition temperature reported for bulk Fe_1+yTe with lowest possible excess Fe content y. The enhanced spin order stability is assigned to a strongly decreased y with respect to the lowest values achievable in bulk crystal growth, and effects due to the interface between the FeTe and the topological insulator. The result is relevant for understanding the recent observation of a coexistence of superconducting correlations and spin order in this system.

cond-mat.str-el↗

Electronic Structure of Fe$_{1.08}$Te bulk crystals and epitaxial FeTe thin films on Bi$_2$Te$_3$

The electronic structure of thin films of FeTe grown on Bi$_2$Te$_3$ is investigated using angle-resolved photoemission spectroscopy, scanning tunneling microscopy and first principles calculations. As a comparison, data from cleaved bulk \FeTe taken under the same experimental conditions is also presented. Due to the substrate and thin film symmetry, FeTe thin films grow on Bi$_2$Te$_3$ in three domains, rotated by 0$^{\circ}$, 120$^{\circ}$, and 240$^{\circ}$. This results in a superposition of photoemission intensity from the domains, complicating the analysis. However, by combining bulk and thin film data, it is possible to partly disentangle the contributions from three domains. We find a close similarity between thin film and bulk electronic structure and an overall good agreement with first principles calculations, assuming a p-doping shift of 65~meV for the bulk and a renormalization factor of around 2. By tracking the change of substrate electronic structure upon film growth, we find indications of an electron transfer from the FeTe film to the substrate. No significant change of the film's electronic structure or doping is observed when alkali atoms are dosed onto the surface. This is ascribed to the film's high density of states at the Fermi energy. This behavior is also supported by the ab-initio calculations.

cond-mat.str-el↗

Evidence for a two-fold symmetric superconducting gap in a monolayer of FeSe$_{0.5}$Te$_{0.5}$ on a topological insulator

We present our investigations on the superconducting properties of monolayers of FeSe$_{0.5}$Te$_{0.5}$ grown on the 3D topological insulator Bi$_{2}$Se$_{1.2}$Te$_{1.8}$ using low temperature scanning tunneling spectroscopy (STS). While the morphology and the overall transition temperature resemble those of similarly doped bulk crystals, the spatially resolved spectroscopic data at 1.1K shows a much larger spatial inhomogeneity in the superconducting energy gaps. Despite the gap inhomogeneity all the spectra can be fitted with a two-fold anisotropic s-wave gap function. The two-fold nature of the gap symmetry is evident from the Bogoliubov quasiparticle interference (QPI) pattern which shows distinct C$_{2}$ symmetric scattering intensities. We argue that the gap inhomogeneity emerges as a result of intrinsic disorder in our system similar to disordered conventional superconductors. Even though most of our findings clearly differ from the current understanding of the corresponding bulk system, it provides an ideal platform to study unconventional superconductivity in Fe chalcogenides thinned down to a single layer and in close proximity to a topological insulator.

cond-mat.supr-con↗

Reorientation of the bicollinear antiferromagnetic structure at the surface of Fe$_{1+y}$Te bulk and thin films

Establishing the relation between the ubiquitous antiferromagnetism in the non-superconducting parent compounds of unconventional superconductors and their superconducting phase is believed to be important for the understanding of the complex physics in these materials. Going from the bulk systems to thin films strongly affects the phase diagram of unconventional superconductors. For Fe$_{1+y}$Te, the parent compound of the Fe$_{1+y}$Se$_{1-x}$Te$_x$ superconductors, bulk sensitive neutron diffraction has revealed an in-plane oriented bicollinear antiferromagnetic structure. Here, we show by spin-resolved scanning tunneling microscopy that on the surfaces of bulk Fe$_{1+y}$Te, as well as on thin films grown on the topological insulator Bi$_2$Te$_3$, the spin direction is canted both away from the surface plane and from the high-symmetry directions of the surface unit cell, while keeping the bicollinear magnetic structure. Our results demonstrate that the magnetism at the Fe-chalcogenide surface markedly deviates from a simple in-plane oriented bicollinear antiferromagnetic structure, which implies that the pairing at the surface of the related superconducting compounds might be different from that in the bulk.

cond-mat.str-el↗

Evidence for interfacial superconductivity in a bi-collinear antiferromagnetically ordered FeTe monolayer on a topological insulator

The discovery of high-temperature superconductivity in Fe-based compounds [1,2] has triggered numerous investigations on the interplay between superconductivity and magnetism [3] and, more recently, on the enhancement of transition temperatures through interface effects [4]. It is widely believed that the emergence of optimal superconductivity is intimately linked to the suppression of long-range antiferromagnetic (AFM) order, although the exact microscopic picture of this relationship remains elusive [1] due to the lack of data with atomic spatial resolution [5-7]. Here, we present a spin-polarized scanning tunneling spectroscopy (SP-STS) study of ultrathin FeTe$_{1-x}$Se$_x$ (x = 0, 0.5) films grown on prototypical Bi-based bulk topological insulators. Surprisingly, we find an energy gap at the Fermi level indicating superconducting correlations up to Tc ~ 6 K for one unit cell thin FeTe layers grown on Bi2Te3 substrates, in contrast to the non-superconducting FeTe bulk compound [8]. Moreover, SP-STS reveals that the energy gap spatially coexists with bicollinear AFM order. This finding opens novel perspectives for theoretical studies of competing orders in Fe-based superconductors as well as for experimental investigations of exotic phases in heterostructures of topological insulators and superconducting layers.

cond-mat.supr-con↗

Band gap engineering by Bi intercalation of graphene on Ir(111)

We report on the structural and electronic properties of a single bismuth layer intercalated underneath a graphene layer grown on an Ir(111) single crystal. Scanning tunneling microscopy (STM) reveals a hexagonal surface structure and a dislocation network upon Bi intercalation, which we attribute to a $\sqrt{3}\times\sqrt{3}R30°$ Bi structure on the underlying Ir(111) surface. Ab-initio calculations show that this Bi structure is the most energetically favorable, and also illustrate that STM measurements are most sensitive to C atoms in close proximity to intercalated Bi atoms. Additionally, Bi intercalation induces a band gap ($E_g=0.42\,$eV) at the Dirac point of graphene and an overall n-doping ($\sim 0.39\,$eV), as seen in angular-resolved photoemission spectroscopy. We attribute the emergence of the band gap to the dislocation network which forms favorably along certain parts of the moiré structure induced by the graphene/Ir(111) interface.

cond-mat.mtrl-sci↗

Response of the topological surface state to surface disorder in TlBiSe$_2$

Through a combination of experimental techniques we show that the topmost layer of the topo- logical insulator TlBiSe$_2$ as prepared by cleavage is formed by irregularly shaped Tl islands at cryogenic temperatures and by mobile Tl atoms at room temperature. No trivial surface states are observed in photoemission at low temperatures, which suggests that these islands can not be re- garded as a clear surface termination. The topological surface state is, however, clearly resolved in photoemission experiments. This is interpreted as a direct evidence of its topological self-protection and shows the robust nature of the Dirac cone like surface state. Our results can also help explain the apparent mass acquisition in S-doped TlBiSe$_2$.

cond-mat.mes-hall↗