arXiv subjects

Daniel Wegner

Publications and source records attributed to Daniel Wegner.

29 records · Page 2Linked to original sources

arXiv2016

Visualizing improved spin coupling in molecular magnets

A key to building functional devices on the basis of single molecule magnets in the framework of molecular electronics is the ability to deposit and study these molecules on a surface, because the structural, electronic and magnetic properties of molecules can significantly change upon adsorption. We have used the submolecular resolution of a scanning tunneling microscope to probe the local interactions within two different rationally designed single-molecule-magnet building blocks. A careful analysis of single-molecule spectroscopic maps reveals that the electronic properties are sensitively dependent on the molecular structure so that even small changes can drastically enhance or reduce the intramolecular spin coupling. Due to their planar geometry, these molecules are ideal model systems to study molecular magnetism of surface-supported complexes via scanning probe techniques.

cond-mat.mes-hall↗

arXiv2016

Single-layer MoS$_2$ on Au(111): band gap renormalization and substrate interaction

The electronic structure of epitaxial single-layer MoS$_2$ on Au(111) is investigated by angle-resolved photoemission spectroscopy, scanning tunnelling spectroscopy, and first principles calculations. While the band dispersion of the supported single-layer is close to a free-standing layer in the vicinity of the valence band maximum at $\bar{K}$ and the calculated electronic band gap on Au(111) is similar to that calculated for the free-standing layer, significant modifications to the band structure are observed at other points of the two-dimensional Brillouin zone: At $\barΓ$, the valence band maximum has a significantly higher binding energy than in the free MoS$_2$ layer and the expected spin-degeneracy of the uppermost valence band at the $\bar{M}$ point cannot be observed. These band structure changes are reproduced by the calculations and can be explained by the detailed interaction of the out-of-plane MoS$_2$ orbitals with the substrate.

cond-mat.str-el↗

arXiv2014

Coherent terabit communications with microresonator Kerr frequency combs

Optical frequency combs enable coherent data transmission on hundreds of wavelength channels and have the potential to revolutionize terabit communications. Generation of Kerr combs in nonlinear integrated microcavities represents a particularly promising option enabling line spacings of tens of GHz, compliant with wavelength-division multiplexing (WDM) grids. However, Kerr combs may exhibit strong phase noise and multiplet spectral lines, and this has made high-speed data transmission impossible up to now. Recent work has shown that systematic adjustment of pump conditions enables low phase-noise Kerr combs with singlet spectral lines. Here we demonstrate that Kerr combs are suited for coherent data transmission with advanced modulation formats that pose stringent requirements on the spectral purity of the optical source. In a first experiment, we encode a data stream of 392 Gbit/s on subsequent lines of a Kerr comb using quadrature phase shift keying (QPSK) and 16-state quadrature amplitude modulation (16QAM). A second experiment shows feedback-stabilization of a Kerr comb and transmission of a 1.44 Tbit/s data stream over a distance of up to 300 km. The results demonstrate that Kerr combs can meet the highly demanding requirements of multi-terabit/s coherent communications and thus offer a solution towards chip-scale terabit/s transceivers.

physics.optics↗

arXiv2013

Unraveling orbital hybridization of triplet emitters at the metal-organic interface

We have investigated the structural and electronic properties of phosphorescent planar platinum(II) complexes at the interface of Au(111) with submolecular resolution using combined scanning tunneling microscopy and spectroscopy as well as density functional theory. Our analysis shows that molecule-substrate coupling and lateral intermolecular interactions are weak. While the ligand orbitals remain essentially unchanged upon contact to the substrate, we found modified electronic behavior at the Pt atom due to local hybridization and charge transfer to the substrate. Thus, this novel class of phosphorescent molecules exhibits well-defined and tunable interaction with its local environment.

cond-mat.mes-hall↗

arXiv2013

Finding the Rashba-type spin-splitting from interband scattering in quasiparticle interference maps

We have studied the BiCu$_2$/Cu(111) surface alloy using low-temperature scanning tunneling microscopy and spectroscopy. We observed standing waves caused by scattering off defects and step edges. Different from previous studies on similar Rashba-type surfaces, we identified multiple scattering vectors that originate from various intraband as well as interband scattering processes. A detailed energy-dependent analysis of the standing-wave patterns enables a quantitative determination of band dispersions, including the Rashba splitting. The results are in good agreement with ARPES data and demonstrate the usefulness of this strategy to determine the band structure of Rashba systems. The lack of other possible scattering channels will be discussed in terms of spin conservation and hybridization effects. The results open new possibilities to study spin-dependent scattering on complex spin-orbit coupled surfaces.

cond-mat.mtrl-sci↗

arXiv2013

Adsorption site determination of a molecular monolayer via inelastic tunneling

We have combined scanning tunneling microscopy with inelastic electron tunneling spectroscopy (IETS) and density functional theory (DFT) to study a tetracyanoethylene monolayer on Ag(100). Images show that the molecules arrange in locally ordered patterns with three non-equivalent, but undeterminable, adsorption sites. While scanning tunneling spectroscopy only shows subtle variations of the local electronic structure at the three different positions, we find that vibrational modes are very sensitive to the local atomic environment. IETS detects sizeable mode frequency shifts of the molecules located at the three topographically detected sites, which permits us to determine the molecular adsorption sites through identification with DFT calculations.

cond-mat.mtrl-sci↗

arXiv2013

Hybridisation at the organic-metal interface: a surface-scientific analogue of Hückel's rule?

We demonstrate that cyclooctatetraene (COT) can be stabilised in different conformations when adsorbed on different noble-metal surfaces due to varying molecule-substrate interaction. While at first glance the behaviour seems to be in accordance with Hückel's rule, a theoretical analysis reveals no significant charge transfer. The driving mechanism for the conformational change is hybridisation at the organic-metal interface and does not necessitate any charge transfer.

cond-mat.mes-hall↗

arXiv2009

Tuning Molecule-Mediated Spin Coupling in Bottom-Up Fabricated Vanadium-TCNE Nanostructures

We have fabricated hybrid magnetic complexes from V atoms and tetracyanoethylene (TCNE) ligands via atomic manipulation with a cryogenic scanning tunneling microscope. Using tunneling spectroscopy we observe spin-polarized molecular orbitals as well as Kondo behavior. For complexes having two V atoms, the Kondo behavior can be quenched for different molecular arrangements, even as the spin-polarized orbitals remain unchanged. This is explained by variable spin-spin (i.e., V-V) ferromagnetic coupling through a single TCNE molecule, as supported by density functional calculations.

cond-mat.mtrl-sci↗

arXiv2009

Indication of a non-magnetic surface layer on a magnetic single crystal

The structural and electronic properties of the surfaces of Sm(0001) and Eu/Gd(0001) were studied by scanning tunneling microscopy and spectroscopy at temperatures between 10 and 110 K. In both systems, an unoccupied surface state is observed that exhibits a temperature-dependent splitting into two states for Eu/Gd(0001), while it is unsplit on Sm(0001). This strongly indicates that the divalent outermost surface layer of Sm(0001) is non-magnetic despite the antiferromagnetic trivalent Sm substrate. These findings open new opportunities for magnetic studies of ultra-thin Sm films.

cond-mat.mtrl-sci↗

arXiv2008

Strongly reshaped organic-metal interfaces: Tetracyanoethylene on Cu(100)

The interaction of the strong electron-acceptor tetracyanoethylene (TCNE) with the Cu(100) surface has been studied with scanning tunneling microscopy experiments and first-principles density functional theory calculations. We compare two different adsorption models with the experimental results and show that the molecular self-assembly is caused by a strong structural modification of the Cu(100) surface rather than the formation of a coordination network by diffusing Cu adatoms. Surface atoms become highly buckled and the chemisorption of TCNE is accompanied by a partial charge-transfer.

cond-mat.mtrl-sci↗

arXiv2007

Spatially-resolved electronic and vibronic properties of single diamondoid molecules

Diamondoids are a unique form of carbon nanostructure best described as hydrogen-terminated diamond molecules. Their diamond-cage structures and tetrahedral sp3 hybrid bonding create new possibilities for tuning electronic band gaps, optical properties, thermal transport, and mechanical strength at the nanoscale. The recently-discovered higher diamondoids (each containing more than three diamond cells) have thus generated much excitement in regards to their potential versatility as nanoscale devices. Despite this excitement, however, very little is known about the properties of isolated diamondoids on metal surfaces, a very relevant system for molecular electronics. Here we report the first molecular scale study of individual tetramantane diamondoids on Au(111) using scanning tunneling microscopy and spectroscopy. We find that both the diamondoid electronic structure and electron-vibrational coupling exhibit unique spatial distributions characterized by pronounced line nodes across the molecular surfaces. Ab-initio pseudopotential density functional calculations reveal that the observed dominant electronic and vibronic properties of diamondoids are determined by surface hydrogen terminations, a feature having important implications for designing diamondoid-based molecular devices.

cond-mat.mtrl-sci↗