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Wulf Wulfhekel

Publications and source records attributed to Wulf Wulfhekel.

44 records · Page 3Linked to original sources
arXiv2016

Coupling to real and virtual phonons in tunneling spectroscopy of superconductors

Fine structures in the tunneling spectra of superconductors have been widely used to identify fingerprints of the interaction responsible for Cooper pairing. Here we show that for scanning tunneling microscopy (STM) of Pb, the inclusion of inelastic tunneling processes is crucial for the proper interpretation of these fine structures. For STM the usual McMillan inversion algorithm of tunneling spectra must therefore be modified to include inelastic tunneling events, an insight that is crucial for the identification of the pairing glue in conventional and unconventional superconductors alike.

cond-mat.supr-con↗
arXiv2015

Scanning Tunneling Spectroscopy on SrFe$\mathrm{_2}$(As$\mathrm{_{1-x}}$P$\mathrm{_x}$)$\mathrm{_2}$

We investigated SrFe$\mathrm{_2}$(As$\mathrm{_{1-x}}$P$\mathrm{_x}$)$\mathrm{_2}$ single crystals with four different phosphorus concentrations x in the superconducting phase (x = 0.35, 0.46) and in the magnetic phase (x = 0, 0.2). The superconducting samples display a V-shaped superconducting gap, which suggests nodal superconductivity. Furthermore we determined the superconducting coherence length by measuring the spatially resolved superconducting density of states (DOS). Using inelastic tunneling spectroscopy we investigated excitations in the samples with four different phosphorus concentrations. Inelastic peaks are related to bosonic modes. Phonon and non-phonon mechanism for the origin of these peaks are discussed.

cond-mat.supr-con↗
arXiv2015

Magnetic adatoms as memory bits: A quantum master equation analysis

Due to underlying symmetries the ground states of magnetic adatoms may be highly stable, which opens perspectives for application as single-atom memory. A specific example is a single holmium atom (with $J=8$) on a platinum (111) surface for which exceptionally long lifetimes were observed in recent scanning tunneling microscopy studies. For control and read-out the atom must be coupled to electronic contacts. Hence the spin dynamics of the system is governed by a quantum master equation. Our analysis shows that in general it cannot be reduced to a classical master equation in the basis of the unperturbed crystal-field Hamiltonian. Rather, depending on parameters and control fields, "environment induced superselection" principles choose the appropriate set of basis states, which in turn determines the specific relaxation channels and lifetimes. Our simulations suggest that in ideal situations the lifetimes should be even longer than observed in the experiment. We, therefore, investigate the influence of various perturbations. We also study the initialization process of the state of the Ho atom by applied voltage pulses and conclude that fast, high fidelity preparation, on a $100\,\text{ns}$ timescale, should be possible.

cond-mat.mes-hall↗
arXiv2014

Local measurement of the Eliashberg function of Pb islands: enhancement of electron-phonon coupling by quantum well states

Inelastic tunneling spectroscopy of Pb islands on Cu(111) obtained by scanning tunneling microscopy below 1K provides a direct access to the local Eliashberg function of the islands with high energy resolution. The Eliashberg function describes the electron-phonon interaction causing conventional superconductivity. The measured Eliashberg function strongly depends on the local thickness of the Pb nanostructures and shows a sharp maximum when quantum well states of the Pb islands come close to the Fermi energy. Ab initio calculations reveal that this is related to enhanced electron-phonon coupling at these thicknesses.

cond-mat.supr-con↗
arXiv2013

C58 on Au(111): a scanning tunneling microscopy study

C58 fullerenes were adsorbed onto room temperature Au(111) surface by low-energy (~6 eV) cluster ion beam deposition under ultrahigh vacuum conditions. The topographic and electronic properties of the deposits were monitored by means of scanning tunnelling microscopy (STM at 4.2 K). Topographic images reveal that at low coverages fullerene cages are pinned by point dislocation defects on the herringbone reconstructed gold terraces (as well as by step edges). At intermediate coverages, pinned monomers, act as nucleation centres for the formation of oligomeric C58 chains and 2D islands. At the largest coverages studied, the surface becomes covered by 3D interlinked C58 cages. STM topographic images of pinned single adsorbates are essentially featureless. The corresponding local densities of states are consistent with strong cage-substrate interactions. Topographic images of [C58]n oligomers show a stripe-like intensity pattern oriented perpendicular to the axis connecting the cage centers. This striped pattern becomes even more pronounced in maps of the local density of states. As supported by density functional theory, DFT calculations, and also by analogous STM images previously obtained for C60 polymers (M. Nakaya et al., J. Nanosci. Nanotechnol. 11, 2829 (2011)), we conclude that these striped orbital patterns are a fingerprint of covalent intercage bonds. For thick C58 films we have derived a band gap of 1.2 eV from scanning tunnelling spectroscopy data, STS, confirming that the outermost C58 layer behaves as a wide band semiconductor.

cond-mat.mes-hall↗
arXiv2012

Parity effect in ground state localization of antiferromagnetic chains coupled to a ferromagnet

We investigate the ground states of antiferromagnetic Mn nanochains on Ni(110) by spin-polarized scanning tunneling microscopy in combination with theory. While the ferrimagnetic linear trimer experimentally shows the predicted collinear classical ground state, no magnetic contrast was observed for dimers and tetramers where non-collinear structures were expected based on ab-initio theory. This striking observation can be explained by zero-point energy motion for even numbered chains derived within a classical equation of motion leading to non classical ground states. Thus, depending on the parity of the chain length, the system shows a classical or a quantum behavior.

cond-mat.mes-hall↗
arXiv2011

Magnetoresistance through a single molecule

The use of single molecules to design electronic devices is an extremely challenging and fundamentally different approach to further downsizing electronic circuits. Two-terminal molecular devices such as diodes were first predicted [1] and, more recently, measured experimentally [2]. The addition of a gate then enabled the study of molecular transistors [3-5]. In general terms, in order to increase data processing capabilities, one may not only consider the electron's charge but also its spin [6,7]. This concept has been pioneered in giant magnetoresistance (GMR) junctions that consist of thin metallic films [8,9]. Spin transport across molecules, i.e. Molecular Spintronics remains, however, a challenging endeavor. As an important first step in this field, we have performed an experimental and theoretical study on spin transport across a molecular GMR junction consisting of two ferromagnetic electrodes bridged by a single hydrogen phthalocyanine (H2Pc) molecule. We observe that even though H2Pc in itself is nonmagnetic, incorporating it into a molecular junction can enhance the magnetoresistance by one order of magnitude to 52%.

cond-mat.mes-hall↗