Publications by authors named "Radican K"

Catalytic activity is of pivotal relevance in enabling efficient and selective synthesis processes. Recently, covalent coupling reactions catalyzed by solid metal surfaces opened the rapidly evolving field of on-surface chemical synthesis. Tailored molecular precursors in conjunction with the catalytic activity of the metal substrate allow the synthesis of novel, technologically highly relevant materials such as atomically precise graphene nanoribbons.

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Experiment and computer simulations were conducted in order to study the adsorption of the phthalocyanine molecules H2Pc and CuPc on the h-BN/Rh(111) nanomesh. We combine STM investigations with the exploration of the potential energy surface as resulting from density functional theory calculations. Both approaches indicate a pronounced adsorption selectivity in the so called pore regions of the h-BN nanomesh, whereas the adsorption energy landscape in the pore turns out to be very shallow.

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Charge-orbital ordering is commonly present in complex transition metal oxides and offers interesting opportunities for novel electronic devices. In this work, we demonstrate for the first time that the magnetization states of the spin valve can be directly manipulated by charge-orbital ordering. We investigate the interlayer exchange coupling (IEC) between two epitaxial magnetite layers separated by a nonmagnetic epitaxial MgO dielectric.

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Understanding molecular switching between different charge states is crucial to further progress in molecule-based nano-electronic devices. Herein we have employed scanning tunnelling microscopy to visualize different charge states of a single C60 molecule within a molecular layer grown on the WO2/W(110) surface. The results obtained demonstrate that individual C60 molecules within the layer switch between neutral and negatively charged states in the temperature range of 220-260 K over the time scale of the experiment.

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The high temperature oxidation of the Pt(111) surface with molecular oxygen has been studied using scanning tunnelling microscopy and low energy electron diffraction (LEED). Results indicate a self-limited growth of well-ordered PtO2 nanoclusters which have an O-Pt-O trilayer structure. Each nanocluster has a triangular shape and nucleates at the Pt(111) surface step edge due to the mobility of Pt atoms.

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We report on the formation of equilateral triangular clusters hollow inside with 5-6 atoms per side, self-assembled on Ni adislands grown on Rh(111). The observation of standing wave patterns on the Ni adislands and the Rh(111) indicates that the self-assembly is mediated by Friedel oscillations. In this context, we propose a model based on the energy of interaction between adsorbates, which explains the formation of the clusters as a result of the assembly of rows of 5-6 adatoms.

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We report on scanning tunneling microscopy studies of the Cu(014)-O surface using MnNi tips. Remarkably, the results show a regular apparent doubling of surface atomic rows in the {110} direction. A qualitative explanation of this feature based on tight binding and density functional theory calculations of the electronic structure of the tip is presented.

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Advanced clinical information systems have been proposed to improve patient care in terms of safety, effectiveness, and efficiency. In order to be effective, such systems require detailed patient-specific clinical information in a form easily reviewed by clinicians. We have developed a patient summary worksheet for use in outpatient clinics, which presents a structured overview of patient health information.

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