Topic
Scanning tunneling spectroscopy
About: Scanning tunneling spectroscopy is a research topic. Over the lifetime, 7886 publications have been published within this topic receiving 213828 citations.
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TL;DR: In this paper, a review of the recent scanning tunneling microscopy (STM) studies on nanoclusters supported on TiO2(110) is presented, focusing on the system Au TiO 2 (110).
234 citations
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233 citations
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TL;DR: The combination of nanographenes and STM/STS, with the PAHs self-assembled in oriented molecular mono- or bilayers at the interface between an organic solution and the basal plane of graphite and contacted by the STM tip, is a simple, reliable, and versatile system for developing the fundamental concepts of molecular electronics.
Abstract: Single-molecule electronics, that is, realizing novel electronic functionalities from single (or very few) molecules, holds promise for application in various technologies, including signal processing and sensing. Nanographenes, which are extended polycyclic aromatic hydrocarbons (PAHs), are highly attractive subjects for studies of single-molecule electronics because the electronic properties of their flat conjugated systems can be varied dramatically through synthetic modification of their sizes and topologies. Single nanographenes provide high tunneling currents when adsorbed flat onto conducting substrates, such as graphite. Because of their chemical inertness, nanographenes interact only weakly with these substrates, thereby preventing the need for special epitaxial structure matching. Instead, self-assembly at the interface between a conducting solid, such as the basal plane of graphite, and a nanographene solution generally leads to highly ordered monolayers. Scanning tunneling spectroscopy (STS) a...
233 citations
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TL;DR: Understanding of the interaction of a single magnetic impurity with the conduction electrons of the nonmagnetic host has been considerably deepened and new insight has emerged by taking advantage of quantum size effects in the metallic support and decoupling the magnetic adatom from the supporting host metal.
Abstract: The present topical review focuses on recent advances concerning an intriguing phenomenon in condensed matter physics, the scattering of conduction electrons at the localized spin of a magnetic impurity: the Kondo effect. Spectroscopic signatures of this effect have been observed in the past by high-resolution photoemission which, however, has the drawback of averaging over a typical surface area of 1 mm(2). By combining the atomic-scale spatial resolution of the scanning tunneling microscope (STM) with an energy resolution of a few tens of mu eV achievable nowadays in scanning tunneling spectroscopy (STS), and by exposing the magnetic adatom to external magnetic fields, our understanding of the interaction of a single magnetic impurity with the conduction electrons of the nonmagnetic host has been considerably deepened. New insight has emerged by taking advantage of quantum size effects in the metallic support and by decoupling the magnetic adatom from the supporting host metal, for instance by embedding it inside a molecule or by separating it by an ultrathin insulating film from the metal surface. In this way, Kondo resonances and Kondo temperatures can be tailored and manipulated by changing the local density of states of the environment. In the weak coupling limit between a Kondo impurity and a superconductor only a convolution of tip and sample DOS is observed while for strongly coupled systems midgap states appear, indicating superconducting pair breaking. Magnetic impurities with co-adsorbed hydrogen on metallic surfaces show pseudo-Kondo resonances owing to very low-energy vibrational excitations detected by inelastic tunneling spectroscopy. One of the most recent achievements in the field has been the clarification of the role of magnetic anisotropy in the Kondo effect for localized spin systems with a spin larger than S = 1/2.
231 citations
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TL;DR: This work investigates the spin- and energy-dependent tunneling through a single organic molecule (CoPc) adsorbed on a ferromagnetic Fe thin film, spatially resolved by low-temperature spin-polarized scanning tunneling microscopy.
Abstract: We investigate the spin- and energy-dependent tunneling through a single organic molecule (CoPc) adsorbed on a ferromagnetic Fe thin film, spatially resolved by low-temperature spin-polarized scanning tunneling microscopy. Interestingly, the metal ion as well as the organic ligand show a significant spin dependence of tunneling current flow. State-of-the-art ab initio calculations including also van der Waals interactions reveal a strong hybridization of molecular orbitals and substrate $3d$ states. The molecule is anionic due to a transfer of one electron, resulting in a nonmagnetic ($S=0$) state. Nevertheless, tunneling through the molecule exhibits a pronounced spin dependence due to spin-split molecule-surface hybrid states.
231 citations