This review presents recent progress concerning the organization of nucleobases on highly ordered pyrolytic graphite (HOPG), mica, Cu(110) and Au(111) surfaces, followed by their studies using microscopy methods such as atomic force microscopy (AFM), scanning tunneling microscopy (STM) and transmission electron microscopy (TEM). Interesting research prospects related to surface patterning by nucleobases, nucleobase-functionalized carbon nanotubes (CNTs) and metal-nucleobase coordination polymers are also discussed, which offer a wide array of functional molecules for advanced applications. Nucleobases and their analogs are able to invoke non-covalent interactions such as π-π stacking and hydrogen bonding, and possess the required framework to coordinate metal ions, giving rise to fascinating supramolecular architectures. The latter could be transferred to conductive substrates, such as HOPG and gold, for assessment by high-end tunneling microscopy under various conditions. Clear understanding of the principles governing nucleobase self-assembly and metal ion complexation, and precise control over generation of functional architectures, might lead to custom assemblies for targeted nanotechnological and nanomaterial applications.
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http://dx.doi.org/10.1039/c8ra03903h | DOI Listing |
Angew Chem Int Ed Engl
January 2025
Università di Milano-Bicocca, Dipartimento di Scienza dei Materiali, via Cozzi 55, 20125, Milano, ITALY.
Confined single metal atoms in graphene-based materials have proven to be excellent catalysts for several reactions and promising gas sensing systems. However, whether the chemical activity arises from the specific type of metal atom or is a direct consequence of the confinement itself remains unclear. In this work, through a combined density functional theory and experimental surface science study, we address this question by investigating Co and Ni single atoms embedded in graphene (Gr) on a Ni(111) support.
View Article and Find Full Text PDFNanoscale
January 2025
Physics Department E20, School of Natural Sciences, Technical University of Munich, Garching, 85748, Germany.
-Armchair graphene nanoribbons (nAGNRs) are promising components for next-generation nanoelectronics due to their controllable band gap, which depends on their width and edge structure. Using non-metal surfaces for fabricating nAGNRs gives access to reliable information on their electronic properties. We investigated the influence of light and iron adatoms on the debromination of 4,4''-dibromo--terphenyl precursors affording poly(-phenylene) (PPP as the narrowest GNR) wires through the Ullmann coupling reaction on a rutile TiO(110) surface, which we studied by scanning tunneling microscopy and X-ray photoemission spectroscopy.
View Article and Find Full Text PDFAcc Chem Res
January 2025
Department of Chemistry, University of California, Berkeley, California 94720, United States.
ConspectusThe electronic properties of atomically thin van der Waals (vdW) materials can be precisely manipulated by vertically stacking them with a controlled offset (for example, a rotational offset─i.e., twist─between the layers, or a small difference in lattice constant) to generate moiré superlattices.
View Article and Find Full Text PDFInorg Chem
January 2025
School of Materials Science and Engineering, Taizhou University, Taizhou 318000, China.
The substantial structural defects frequently observed in fabricated transition-metal dichalcogenide (TMD) samples inevitably affect the device performance. The molybdenum telluride (MoTe) monolayer can easily generate phase transitions between the 1H and 1T' phases due to a small energy barrier. However, distinguishing and identifying various defects during experiments is challenging.
View Article and Find Full Text PDFNanoscale
January 2025
Center for Energy and Environmental Sciences, Paul Scherrer Institute, Forschungsstrasse 111, 5232, Villigen, Switzerland.
The strong influence of surface adsorbates on the morphology of a catalyst is exemplified by studying a silver surface with and without deposited zinc oxide nanoparticles upon exposure to reaction gases used for carbon dioxide hydrogenation. Ambient pressure X-ray photoelectron spectroscopy and scanning tunneling microscopy measurements indicate accumulation of carbon deposits on the catalyst surface at 200 °C. While oxygen-free carbon species observed on pure silver show a strong interaction and decorate the atomic steps on the catalyst surface, this decoration is not observed for the oxygen-containing species observed on the silver surface with additional zinc oxide nanoparticles.
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