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Individual magnetic transition metal dopants in a solid host usually exhibit relatively small spin excitation energies of a few meV. Using scanning tunneling microscopy and inelastic electron tunneling spectroscopy (IETS) techniques, we have observed a high spin excitation energy around 36 meV for an individual Co substitutional dopant in ultrathin NaCl films. In contrast, the Cr dopant in the NaCl film shows much lower spin excitation energy around 2.5 meV. Electronic multiplet calculations combined with first-principles calculations confirm the spin excitation induced IETS, and quantitatively reveal the out-of-plane magnetic anisotropies for both Co and Cr. They also allow reproducing the experimentally observed redshift in the spin excitations of Co dimers and ascribe it to a charge and geometry redistribution., (Creative Commons Attribution license.)

We investigated the topological insulator (TI) Bi 2 Te 3 in four different environments (ambient, ultra-high vacuum (UHV), nitrogen gas and organic solvent environment) using scanning probe microscopy (SPM) techniques. Upon prolonged exposure to ambient conditions and organic solvent environments the cleaved surface of the pristine Bi 2 Te 3 is observed to be strongly modified during SPM measurements, while imaging of freshly cleaved Bi 2 Te 3 in UHV and nitrogen gas shows considerably less changes of the Bi 2 Te 3 surface. We conclude that the reduced surface stability upon exposure to ambient conditions is triggered by adsorption of molecular species from ambient, including H 2 O, CO 2 , etc which is verified by Auger electron spectroscopy. Our findings of the drastic impact of exposure to ambient on the Bi 2 Te 3 surface are crucial for further in-depth studies of the intrinsic properties of the TI Bi 2 Te 3 and for potential applications that include room temperature TI based devices operated under ambient conditions.

We report on the adsorption of Te adatoms on Au(1 1 1), which are identified and investigated relying on scanning tunnelling microscopy, Auger electron spectroscopy, and density functional theory. The Te adatoms lift the 23  ×  √3 surface reconstruction of the Au(1 1 1) support and their organization is similar to that of previously reported chalcogen adatoms on Au(1 1 1), which are also known to lift the herringbone reconstruction and can adopt a (√3  ×  √3)R30° structure. The adatoms show strong interaction with the Au(1 1 1) surface, resulting in scattering and confinement of the Au surface state (SS) electrons near the Fermi level. More remarkably, scanning tunnelling spectroscopy reveals the existence of an electronic resonance at high voltages well above the Fermi level. This resonance can be interpreted as a bound state that is split off from the bottom of the Au(1 1 1) bulk conduction band. A similar split-off state may exist for other types of adatoms on metallic surfaces that exhibit a surface band gap.

Atomic-level substitutional doping can significantly tune the electronic properties of graphene. Using low-temperature scanning tunneling microscopy and spectroscopy, the atomic-scale crystalline structure of graphene grown on polycrystalline Cu, the distribution of nitrogen dopants and their effect on the electronic properties of graphene were investigated. Both the graphene sheet growth and nitrogen doping were performed using microwave plasma-enhanced chemical vapor deposition. The results indicated that the nitrogen dopants preferentially sit at the grain boundaries of the graphene sheets and confirmed that plasma treatment is a potential method to incorporate foreign atoms into the graphene lattice to tailor the graphene's electronic properties.

We investigated the growth and the electronic properties of crystalline NaCl layers on Au(111) surfaces by means of cryogenic scanning tunneling microscopy and spectroscopy under ultra-high vacuum conditions. Deposition of NaCl on Au(111) at room temperature yields bilayer NaCl islands, which can be transformed into trilayer NaCl islands by post-annealing. Upon NaCl adsorption, the Au(111) Shockley surface state becomes an interface state (IS) at the NaCl/Au(111) interface. Using Fourier-transform images of maps of the local density of states, the energy versus wave vector dispersions of the IS and the Au(111) bulk states are determined. The dispersion of both states is found to depend strongly on the thickness of the adsorbed NaCl layer.

The formation of a novel surface reconstruction upon Co deposition on freshly cleaved Ge(111)2 × 1 surfaces is studied by means of scanning tunneling microscopy (STM) at 4.5 K. Previously we demonstrated that at this low substrate temperature the deposited Co atoms remain immobile after they become embedded underneath the Ge(111)2 × 1 surface. We now demonstrate that at higher substrate temperatures the embedded Co atoms are able to diffuse below the surface in a direction parallel to the upper π-bonded chain rows. This one-dimensional temperature-induced mobility results in subsurface accumulation of Co atoms at atomic steps, at domain boundaries and on atomically flat Ge terraces at, e.g., vacancies or adatoms, where reconstructed Co/Ge intermixing layers are formed. Voltage dependent STM images reveal that the Co related surface reconstruction locally exhibits an ordered atomic structure with the same inter-atomic distance as that of the initial 2 × 1 reconstructed pure Ge(111) surface. On the other hand, the presence of the Co results in a doubling of the periodicity along the [21[overline]1[overline]] direction in the STM images, which can be related to the modified electronic properties of the π-bonded chains.

Discrete image-potential states (ISs) are revealed at double-walled carbon nanotubes by means of scanning tunneling microscopy (STM) and scanning tunneling spectroscopy (STS) in the distance-voltage z(V) spectroscopy mode. The nanotubes are supported by flat Au(111) substrates. Due to the high sensitivity of the hot IS electrons to local variations of the surface potential, they can be considered as a sensitive probe to investigate interactions with the supporting substrate and impurities or defects at the nanotube surface. ISs provide information on the local electronic structure as well as on the electron dynamics at supported nanotubes.

Deposition of Co atoms on Au(111) surfaces leads to the formation of self-organized bilayer Co nanowires at the step edges between adjacent narrow Au(111) terraces. Scanning tunneling microscopy and spectroscopy at low temperatures is used to probe the influence of the finite dimensions on the local density of states for both the Co wires and the narrow Au terraces. Confinement of Au surface state electrons to narrow Au terraces causes a shift of the Au surface state onset energy to higher energies. For the Co nanowires discrete energy levels are observed. Moreover, standing wave patterns occur at the surface of both the Au and the Co. The patterns increase in complexity with increasing energy. All Co nanowires formed at the edges of narrow Au terraces reveal a characteristic maximum in the local density of states at a significantly different energy when compared to the Co islands that are formed on large Au terraces. The experimental results can be interpreted in terms of a simple particle-in-a-box model.

By means of ion bombardment of clean Au(111) films, atomically flat nanoparticles of various shapes and sizes were created, ranging from several tens of nm(2) down to only a few nm(2). Both two-dimensional Au islands as well as one-dimensional Au nanowire-like structures have been investigated by means of low-temperature scanning tunneling microscopy and spectroscopy. We were able to probe their local electronic structure in a broad energy range, which was found to be dominated by pronounced size-dependent confinement effects. Mapping of the local density of states revealed complex standing wave patterns that arise due to interference of scattered Au surface state electrons at the edges of the Au nanoparticles. The observed phenomena could be modeled with high accuracy by theoretical particle-in-a-box calculations based on a variational method that can be applied to '2D boxes' of arbitrary polygonal shape and that we have previously successfully applied to explain the electronic wave patterns on Co islands on Au(111). Our findings support the general validity of this particle-in-a-box model.

If graphene is ever going to live up to the promises of future nanoelectronic devices, an easy and cheap route for mass production is an essential requirement. A way to extend the capabilities of plasma-enhanced chemical vapour deposition to the synthesis of freestanding few-layer graphene is presented. Micrometre-wide flakes consisting of four to six atomic layers of stacked graphene sheets have been synthesized by controlled recombination of carbon radicals in a microwave plasma. A simple and highly reproducible technique is essential, since the resulting flakes can be synthesized without the need for a catalyst on the surface of any substrate that withstands elevated temperatures up to 700 °C. A thorough structural analysis of the flakes is performed with electron microscopy, x-ray diffraction, Raman spectroscopy and scanning tunnelling microscopy. The resulting graphene flakes are aligned vertically to the substrate surface and grow according to a three-step process, as revealed by the combined analysis of electron microscopy and x-ray photoelectron spectroscopy.