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Detailed measurements of state resolved inelastic scattering of N[SUB2] from Ru (0001) are reported for a wide range of initial energies (0-3 eV) and angles of incidence. The ion time-of-flight resonantly enhanced multiphoton ionization (REMPI) detection scheme developed here and used with cw molecular beams simultaneously measures the internal quantum state and translational energy normal to the sample surface. Doppler broadening of the REMPI spectrum of scattered particles (yields the dispersion in scattering out of plane. The results are qualitatively similar to inelastic N[SUB2] scattering studies for a wide variety of other metal surfaces; i.e., no observable vibrational excitation, weak rotational excitation described as a Boltzmann distribution, strong surface excitation depending upon the incident normal energy, and an anticorrelation between rotational and surface excitation. The absence of any vibrational excitation at E≈3 eV is inconsistent with adiabatic model dynamics based on the ab initio potential-energy surface. It is, however, consistent with a strong nonadiabatic damping of vibration to electron-hole pairs in the region of the barrier. This same suggestion was previously found necessary to rationalize unusual dissociative adsorption and associative desorption of N[SUB2] on Ru(0001). [ABSTRACT FROM AUTHOR]

We report on an atomic-scale study of the Kondo lattice compound YbAl3 using scanning tunneling microscopy (STM) and spectroscopy (STS). An analysis of the surface orientation and structure is performed based on STM images containing more than one crystal facet. We compare tunneling spectra acquired on different facets and discuss their relation with the temperature scales observed in measurements of bulk quantities and the states observed in photoemission spectra. On specific facets, we observe strong additional resonances close to the Fermi energy which are not consistent with the characteristic energy scales found in bulk measurements, and which we interpret in terms of a modified Kondo stale of the near-surface Ytterbium atoms. [ABSTRACT FROM AUTHOR]

We have used a scanning tunneling microscope operated under ultrahigh vacuum conditions to investigate an oxo-vanadium-salen complex V(O)salen, that has potential applications as qubits in future quantum-based technologies. The adsorption and self-assembly of V(O)salen on a range of single crystal metal surfaces and nanoislands and the influence of substrate morphology and reactivity has been measured. On the close-packed flat Ag(111) and Cu(111) surfaces, the molecules adsorb isolated or form small clusters arranged randomly on the surface, whereas structured adsorption occurs on two types of Co nanoislands; Co grown on Ag(111) and Ag capped Co islands grown on Cu(111), both forming a Moiré pattern at the surface. The adsorption configuration can by scanning tunneling spectroscopy be linked to the geometric and electronic properties of the substrates and traced back to a Co d-related surface state, illustrating how the modulated reactivity can be used to engineer a pattern of adsorbed molecules on the nanoscale.

Terahertz time-domain spectroscopy (THz-TDS) can be used to map spatial variations in electrical properties such as sheet conductivity, carrier density, and carrier mobility in graphene. Here, we consider wafer-scale graphene grown on germanium by chemical vapor deposition with non-uniformities and small domains due to reconstructions of the substrate during growth. The THz conductivity spectrum matches the predictions of the phenomenological Drude-Smith model for conductors with non-isotropic scattering caused by backscattering from boundaries and line defects. We compare the charge carrier mean free path determined by THz-TDS with the average defect distance assessed by Raman spectroscopy, and the grain boundary dimensions as determined by transmission electron microscopy. The results indicate that even small angle orientation variations below 5° within graphene grains influence the scattering behavior, consistent with significant backscattering contributions from grain boundaries., (© 2024. The Author(s).)

Magnetically controlled growing rods (MCGR's) have revolutionized the treatment of early-onset scoliosis (EOS) because painless lengthenings can be done in the outpatient clinic without anesthesia. Untreated EOS leads to respiratory insufficiency and reduced life expectancy. However, MCGR's have inherent complications like non-functioning of the lengthening mechanism. We quantify an important failure mechanism and give advice on how to avoid this complication. The magnetic field strength was measured on new/explanted rods at different distances between the external remote controller and the MCGR and likewise in patients before/after distractions. The magnetic field strength of the internal actuator decayed fast with increasing distances and plateaued at 25-30 mm approximating zero. Two new and 12 explanted MCGRs was used for the lab measurements of the elicited force using a forcemeter. At a distance of 25 mm, the force was reduced to approximately 40% (ca. 100 N) compared to zero distance (ca. 250 N), most so for explanted rods. This is used to point out the importance of minimizing the implantation depth to ensure proper functionality of the rod lengthening in clinical use for EOS patients. A distance of 25 mm from skin to MCGR should be considered a relative contraindication to clinical use in EOS patients., (© 2023. The Author(s).)

We present an extended metal-coordinated structure obtained by deposition of trimesic acid (TMA) onto the Ag(111) surface under ultra-high vacuum conditions followed by annealing to 510 K. Scanning tunneling microscopy and density functional theory calculations reveal the structure to consist of metal clusters containing seven Ag atoms each, coordinated by six dehydrogenated TMA molecules. The molecules are asymmetrically arranged, resulting in a chiral structure. The calculations confirm that this structure has a lower free energy under the experimental conditions than the hydrogen-bonded structures observed after annealing at lower temperatures. We show that the formation of such large metal clusters is possible due to the low adatom formation energy on silver and the relatively strong Ag-O bond in combination with a good lattice match between the structure and the Ag surface.

The balance between molecule-molecule and molecule-surface interactions is a determining factor in the creation of well-ordered organic networks formed by self-assembly on crystalline metal surfaces. We have used a scanning tunneling microscope under ultrahigh vacuum conditions to study the molecular self-assembly of trimesic acid on a surface that is modulated on a comparable nanometer scale as the size of the molecules. This is made of one layer of silver grown on a Cu(111) surface where it forms a periodic reconstruction. It is shown that the self-assembly of trimesic acid at room temperature, where intermolecular interactions are taking place via hydrogen bonds, is strongly disturbed due to the modulated substrate and the spatially varying potential imposed on the molecules. Annealing to 350 K partly deprotonates the molecules and changes the intermolecular interactions to stronger ionic hydrogen bonds. This reduces the influence of the modulated substrate and allows the molecules to self-assemble into long-range ordered networks on the surface. Comparisons are made to self-assembly on the flat surfaces of Ag(111) and Cu(111), where we always find well-ordered molecular networks.

We have studied the growth of Ag on bilayer high Co nanoislands on Cu(111) using scanning tunneling microscopy. Noble metal capping of magnetic nanostructures is known to influence the magnetism and knowledge of the growth is therefore important. We find that Ag preferentially nucleates on the Co nanoislands, initially leaving the free Cu sites clean. Furthermore we observe that those Co islands which are capped with Ag are almost completely capped, thus making a perfect multilayered system of Ag/Co/Cu(111). We observe a (9 × 9) reconstruction of the Ag overlayer on Co/Cu(111).

The surface of single crystal Ag(13)OsO(6) has been investigated using atomic force microscopy. Growth spirals with very large flat terraces, separated by steps of equal height, have been observed. The measured step height of approximately 6.7 Angstrom corresponds to the diameter of one Ag13-icosahedron and identifies the cluster as the key structural building block.

The Kondo resonance of Co adatoms on the Cu(100) and Cu(111) surfaces has been studied by scanning tunneling spectroscopy. We demonstrate the scaling of the Kondo temperature T(K) with the host electron density at the magnetic impurity. The quantitative analysis of the tunneling spectra reveals that the Kondo resonance is dominated by the Cu bulk electrons. While at the Cu(100) surface both tunneling into the hybridized localized state and into the substrate conduction band contribute to the Kondo resonance, the latter channel is found to be dominant for Cu(111).