The assembly of melamine and 2,5-dihydroxy-1,4-benzoquinone results in new "sheet-like" supramolecular crystals that by controlled thermal condensation can be converted to photoactive materials at relativity low temperatures. The condensation temperature alters the materials properties from polymer-like to carbon materials alongside their morphology and elemental ratio. This new method opens the possibility for the synthesis of new organic, photoactive carbon-nitrogen based frameworks at low calcination temperatures with great simplicity. Photodegradation experiments of methylene blue reveal that the obtained materials can perform dye reduction photochemically with visible photons, while at the same time the photogenerated holes oxidize the dye toward small molecular fragments.
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http://dx.doi.org/10.1002/smll.201602445 | DOI Listing |
Small
January 2025
UMR 8182, CNRS, Institut de Chimie Moléculaires et des Matériaux d'Orsay, Université Paris-Saclay, Orsay, 91405, France.
Capturing sunlight to fuel the water splitting reaction (WSR) into O and H is the leitmotif of the research around artificial photosynthesis. Organic semiconductors have now joined the quorum of materials currently dominated by inorganic oxides, where for both families of compounds the bandgaps and energies can be adjusted synthetically to perform the Water Splitting Reaction. However, elaborated and tedious synthetic pathways are necessary to optimize the photophysical properties of organic semiconductors.
View Article and Find Full Text PDFACS Nano
January 2025
Department of Chemistry, University of Chicago, Chicago, Illinois 60637, United States.
Fabricating organic semiconducting materials into large-scale, well-organized architectures is critical for building high-performance molecular electronics. While graphene nanoribbons (GNRs) hold enormous promise for various device applications, their assembly into a well-structured monolayer or multilayer architecture poses a substantial challenge. Here, we report the preparation of length-defined monodisperse GNRs via the integrated iterative binomial synthesis (IIBS) strategy and their self-assembly into submicrometer architectures with long-range order, uniform orientation, as well as regular layers.
View Article and Find Full Text PDFDalton Trans
January 2025
Department of Chemistry, Central Tribal University of Andhra Pradesh (CTUAP), Andhra Pradesh, 535003, India.
Hydrogen is a zero-emissive fuel and has immense potential to replace carbon-emitting fuels in the future. The development of efficient H sensors is essential for preventing hazardous situations and facilitating the widespread usage of hydrogen. Chemiresistors are popular gas sensors owing to their attractive properties such as fast response, miniaturization, simple integration with electronics and low cost.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Institute of Chemistry Chinese Academy of Sciences, Laboratory of Organic Solids, Zhongguancun, 100190, Beijing, CHINA.
Conjugated coordination polymers (c-CPs), a novel class of organic-inorganic hybrid materials, are distinguished by their unique structural characteristics and exceptional charge transport properties. The electronic properties of these materials are critically determined by the constituting coordination atoms, with electron-rich selenol ligands emerging as promising candidates for constructing high-mobility semiconducting c-CPs. Currently, c-CPs incorporating selenium-substituted ligands remain scarce.
View Article and Find Full Text PDFNanoscale
January 2025
Department of Engineering "Enzo Ferrari", (DIEF), Univ. of Modena, Via Vivarelli 10, 41125 Modena, Italy.
Great efforts have been made in the last few decades to realize electronic devices based on organic molecules. A possible approach in this field is to exploit the chirality of organic molecules for the development of spintronic devices, an applicative way to implement the chiral-induced spin selectivity (CISS) effect. In this work we exploit enantiopure tetrathiafulvalene (TTF) derivatives as chiral inducers at the nanoscale.
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