Diamond, as the densest allotrope of carbon, displays a range of exemplary material properties that are attractive from a device perspective. Despite diamond displaying high carbon-carbon bond strength, ultrashort (femtosecond) pulse laser radiation can provide sufficient energy for highly localized internal breakdown of the diamond lattice. The less-dense carbon structures generated on lattice breakdown are subject to significant pressure from the surrounding diamond matrix, leading to highly unusual formation conditions. By tailoring the laser dose delivered to the diamond, it is shown that it is possible to create continuously modified internal tracks with varying electrical conduction properties. In addition to the widely reported conducting tracks, conditions leading to semiconducting and insulating written tracks have been identified. High-resolution transmission electron microscopy (HRTEM) is used to visualize the structural transformations taking place and provide insight into the different conduction regimes. The HRTEM reveals a highly diverse range of nanocarbon structures are generated by the laser irradiation, including many signatures for different so-called diaphite complexes, which have been seen in meteorite samples and seem to mediate the laser-induced breakdown of the diamond. This work offers insight into possible formation methods for the diamond and related nanocarbon phases found in meteorites.
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http://dx.doi.org/10.1021/acsnano.3c07116 | DOI Listing |
Chem Soc Rev
December 2024
State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering, School of Electronic Science and Engineering, College of Environment and Ecology, State Key Laboratory of Marine Environmental Science, Department of Physics, iChEM, IKKEM, Xiamen University, Xiamen 361005, China.
Surface-enhanced Raman spectroscopy (SERS) has evolved significantly over fifty years into a powerful analytical technique. This review aims to achieve five main goals. (1) Providing a comprehensive history of SERS's discovery, its experimental and theoretical foundations, its connections to advances in nanoscience and plasmonics, and highlighting collective contributions of key pioneers.
View Article and Find Full Text PDFSmall
December 2024
Department of Chemical Science and Engineering, Institute of Science Tokyo, 4259 Nagatsuta-cho, Midori-ku, Yokohama, Kanagawa, 226-8501, Japan.
Morphology-controlled synthesis of covalent organic frameworks (COFs) offers significant potential for electrochemical applications. However, controlling the deposition of nanometer-scale COFs on carbon supports remains challenging due to the need for a slow COF generation rate and the dispersion of carbon supports in liquid-phase synthesis. In this study, nanometer-scale COF/carbon composites are fabricated using electrochemically generated acid (EGA) to assist in the formation of imine-type COFs, which are then deposited onto pre-cast nanocarbon supports on an electrode.
View Article and Find Full Text PDFDiscov Nano
December 2024
IMDEA Materials Institute, C/Eric Kandel 2, 28906, Getafe, Madrid, Spain.
New materials for electrical conductors, energy storage, thermal management, and structural elements are required for increased electrification and non-fossil fuel use in transport. Appropriately assembled as macrostructures, nanomaterials can fill these gaps. Here, we critically review the materials science challenges to bridge the scale between the nanomaterials and the large-area components required for applications.
View Article and Find Full Text PDFChem Sci
October 2024
Wydział Chemii, Uniwersytet Wrocławski ul. F. Joliot-Curie 14 50-383 Wrocław Poland
J Phys Chem A
November 2024
Department of Chemistry, Nanoscale Sciences and Technology Institute, Nanocarbon R&D Institute, Wonkwang University, Iksan, Jeonbuk 54538, R.O.K.
We studied the hydroboration of the C fullerene using both B3LYP-D3(BJ)/6-311G(d,p) and M06-2X-D3/6-311G(d,p) levels of theory, incorporating the empirical dispersion interaction, and Fukui index calculations. Potential energy surfaces (PESs) and Gibbs free energy surfaces (GFESs) were calculated for the pathways from four BH adducts (located at the , , , and sites) on the C to eight products formed by the 1,2-addition of BH across the four [6,6]-ring fused bonds (, , , and ) and across the two [5,6]-ring fused bonds ( and ). These pathways are two-step consecutive reactions.
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