We report on electronic transport measurements in rotational square probe configuration in combination with scanning tunneling potentiometry of epitaxial graphene monolayers which were fabricated by polymer-assisted sublimation growth on SiC substrates. The absence of bilayer graphene on the ultralow step edges of below 0.75 nm scrutinized by atomic force microscopy and scanning tunneling microscopy result in a not yet observed resistance isotropy of graphene on 4H- and 6H-SiC(0001) substrates as low as 2%. We combine microscopic electronic properties with nanoscale transport experiments and thereby disentangle the underlying microscopic scattering mechanism to explain the remaining resistance anisotropy. Eventually, this can be entirely attributed to the resistance and the number of substrate steps which induce local scattering. Thereby, our data represent the ultimate limit for resistance isotropy of epitaxial graphene on SiC for the given miscut of the substrate.

A numerical simulation procedure is used to answer some fundamental questions about magnetooptical phenomena. By investigating hypothetical thin buried layers of magnetic material in a non‐magnetic environment of otherwise identical optical properties a suggestive law is derived for the information depth profile of Kerr effect measurements. Differences in phase between contributions from different depth often limit the range of the Kerr effect to a higher degree than absorption. In oxides the profile has usually an oscillating character, but conditions are derived under which these oscillations can be suppressed. The differing phase of sub‐surface contributions connects these considerations with Kamberský's interpretation of the recently discovered magnetooptical gradient effect. Finally, the theoretical and practical possibilities are explored of enhancing the Kerr effect in ultra‐thin films in which all the light is forced to react in a thin layer rather than in the depth of a thick material. In this connection a far‐reaching generalization of Lissberger's limit for the Kerr amplitude in thin film mirror‐based systems is discovered.

We investigate photocurrents driven by femtosecond laser excitation of a (sub)-nanometer tunnel junction in an ultrahigh vacuum low-temperature scanning tunneling microscope (STM). The optically driven charge transfer is revealed by tip retraction curves showing a current contribution for exceptionally large tip-sample distances, evidencing a strongly reduced effective barrier height for photoexcited electrons at higher energies. Our measurements demonstrate that the magnitude of the photo-induced electron transport can be controlled by the laser power as well as the applied bias voltage. In contrast, the decay constant of the photocurrent is only weakly affected by these parameters. Stable STM operation with photoelectrons is demonstrated by acquiring constant current topographies. An effective non-equilibrium electron distribution as a consequence of multiphoton absorption is deduced by the analysis of the photocurrent using a one-dimensional potential barrier model.

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Graphene, the first true two-dimensional material still reveals the most remarkable transport properties among the growing class of two-dimensional materials. Although many studies have investigated fundamental scattering processes, the surprisingly large variation in the experimentally determined resistances associated with a localized defect is still an open issue. Here, we quantitatively investigate the local transport properties of graphene prepared by polymer assisted sublimation growth (PASG) using scanning tunneling potentiometry. PASG graphene is characterized by a spatially homogeneous current density, which allows to analyze variations in the local electrochemical potential with high precision. We utilize this possibility by examining the local sheet resistance finding a significant variation of up to 270% at low temperatures. We identify a correlation of the sheet resistance with the stacking sequence of the 6H-SiC substrate as well as with the distance between the graphene

The search for materials with novel and unusual electronic properties is at the heart of condensed matter physics as well as the basis to develop conceptual new technologies. In this context, the correlated honeycomb transition metal oxides have attracted large attention for both, being a possible experimental realization of the theoretically predicted magnetic Kitaev exchange and the theoretical prospect of topological nontriviality. Mott‐insulating Na2IrO3 is prototypical among these materials, characterized by crystal field splitting, spin–orbit coupling, and Hubbard repulsion being on similar energy scales. Herein, a combined electrical transport and scanning tunneling spectroscopy (STS) study of the surface of sodium iridate cleaved and in situ investigated under ultrahigh vacuum is reported. Temperature‐dependent transport measurements prove the existence of surface conductance with a surprisingly high and temperature‐independent conductivity. STS shows a variety of different spectra. Most importantly, a significant density of states is found within the bandgap of sodium iridate at the surface. Based on the local spectroscopic information, multiple conductive channels with differing nature being simultaneously apparent in this material are discussed.

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