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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Ruben, Mario
Karlsruhe Institute of Technology
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (13/13 displayed)
- 2024Computational demonstration of isomer- and spin-state-dependent charge transport in molecular junctions composed of charge-neutral iron(II) spin-crossover complexescitations
- 2024Unconventional Band Structure via Combined Molecular Orbital and Lattice Symmetries in a Surface‐Confined Metallated Graphdiyne Sheetcitations
- 2023A π‐Conjugated Porphyrin Complex as Cathode Material Allows Fast and Stable Energy Storage in Calcium Batteriescitations
- 2023A π‐Conjugated Porphyrin Complex as Cathode Material Allows Fast and Stable Energy Storage in Calcium Batteries
- 2023Molecular Engineering of Metalloporphyrins for High‐Performance Energy Storage: Central Metal Matterscitations
- 2022Field-Induced Single Molecule Magnetic Behavior of Mononuclear Cobalt(II) Schiff Base Complex Derived from 5-Bromo Vanillincitations
- 2021A self‐conditioned metalloporphyrin as a highly stable cathode for fast rechargeable magnesium batteries
- 2021A Self‐Conditioned Metalloporphyrin as a Highly Stable Cathode for Fast Rechargeable Magnesium Batteriescitations
- 2018Radical-lanthanide ferromagnetic interaction in a TbIII bis-phthalocyaninato complexcitations
- 2018Functionalized Graphdiyne Nanowires: On‐Surface Synthesis and Assessment of Band Structure, Flexibility, and Information Storage Potentialcitations
- 2014Meta-Positioning of Carbonitrile Functional Groups Induces Interfacial Edge-On Phase of Oligophenyl Derivativescitations
- 2013Spin-dependent electronic structure of the Co/Al(OP)3 interfacecitations
- 2011Supramolecular spin valvescitations
Places of action
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article
Functionalized Graphdiyne Nanowires: On‐Surface Synthesis and Assessment of Band Structure, Flexibility, and Information Storage Potential
Abstract
<jats:title>Abstract</jats:title><jats:p>Carbon nanomaterials exhibit extraordinary mechanical and electronic properties desirable for future technologies. Beyond the popular sp<jats:sup>2</jats:sup>‐scaffolds, there is growing interest in their graphdiyne‐related counterparts incorporating both sp<jats:sup>2</jats:sup> and sp bonding in a regular scheme. Herein, we introduce carbonitrile‐functionalized graphdiyne nanowires, as a novel conjugated, one‐dimensional (1D) carbon nanomaterial systematically combining the virtues of covalent coupling and supramolecular concepts that are fabricated by on‐surface synthesis. Specifically, a terphenylene backbone is extended with reactive terminal alkyne and polar carbonitrile (CN) moieties providing the required functionalities. It is demonstrated that the CN functionalization enables highly selective alkyne homocoupling forming polymer strands and gives rise to mutual lateral attraction entailing room‐temperature stable double‐stranded assemblies. By exploiting the templating effect of the vicinal Ag(455) surface, 40 nm long semiconducting nanowires are obtained and the first experimental assessment of their electronic band structure is achieved by angle‐resolved photoemission spectroscopy indicating an effective mass below 0.1<jats:italic>m</jats:italic><jats:sub>0</jats:sub> for the top of the highest occupied band. Via molecular manipulation it is showcased that the novel oligomer exhibits extreme mechanical flexibility and opens unexplored ways of information encoding in clearly distinguishable CN‐phenyl <jats:italic>trans–cis</jats:italic> species. Thus, conformational data storage with density of 0.36 bit nm<jats:sup>−2</jats:sup> and temperature stability beyond 150 K comes in reach.</jats:p>