Photocatalytic systems have attracted research interest as a clean approach to generate energy from abundant sunlight. In this context, developing efficient and robust photocatalytic structures is crucial. Recently, self-assembled organic chromophores have entered the stage as alternatives to both molecular systems and (in)organic semiconductors. Nanostructures made of self-assembled π-conjugated dyes offer, on the one hand, molecular customizability to tune their optoelectronic properties and activities and on the other hand, provide benefits from heterogeneous catalysis that include ease of separation, recyclability and improved photophysical properties. In this contribution, we present recent achievements in constructing supramolecular photocatalytic systems made of chromophores for applications in water splitting, HO evolution, CO reduction, or environmental remediation. We discuss strategies that can be used to prepare ordered photocatalytic systems with an emphasis on the effect of packing between the dyes and the resulting photocatalytic activity. We further showcase supramolecular strategies that allow interfacing the organic nanostructures with co-catalysts, molecules, polymers, and (in)organic materials. The principles discussed here are the foundation for the utilization of these self-assembled materials in photocatalysis.
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http://dx.doi.org/10.1039/d4nr00383g | DOI Listing |
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June 2025
Department of Biology, Faculty of Mathematics and Natural Sciences, Mulawarman University, Samarinda, 75242, Indonesia.
The use of eggshells as a primary source for developing value-added materials has garnered significant attention in recent years due to their effectiveness as an excellent adsorbent and support. In this study, the Solid-State Dispersion (SSD) method was utilized to prepare composite photocatalysts of eggshells (ES)/TiO₂ in various ratios. TiO₂ and eggshell photocatalysts were also employed as control samples.
View Article and Find Full Text PDFJ Colloid Interface Sci
January 2025
School of Resources and Environmental Engineering, Wuhan University of Technology, Wuhan 430070, China. Electronic address:
Antibiotic organic pollutants not only pose a significant threat to human health but also generate a large amount of carbon dioxide (CO) during the treatment process of advanced oxidation processes (AOPs). Herein, the antibiotics aqueous solution was firstly degraded and mineralized by light-assisted peroxymonosulfate (PMS) activation over hollow manganese dioxide (MnO) catalyst and then the corresponding released CO was effectively captured by calcium oxide (CaO) particles in the same sealed reactor, achieving wastewater treatment with zero carbon releasing. Under simulated light conditions, hollow MnO is excited to generate electron-hole pairs.
View Article and Find Full Text PDFChemistry
January 2025
The Hong Kong Polytechnic University, Department of Applied Biology and Chemical Technology, Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hong Hom, Hong Kong (P.R. China), 000000, Hong Kong, HONG KONG.
A series of new (donor)₂-donor-π-acceptor (D2-D-π-A) and (acceptor)₂-donor-π-acceptor (A2-D-π-A) organic photosensitizers based on the framework of (Z)-2-cyano-3-(5-(4-(diphenylamino)phenyl)thiophen-2-yl)acrylic acid have been synthesized and characterized. By incorporating groups with different electron-donating or withdrawing abilities, such as dibenzothiophene (DBT), dibenzofuran (DBF), and triazine (TA), into the triphenylamine segment, their photophysical properties have been regulated. Theoretical calculations were used to explore how various donor-acceptor combinations influence their hydrogen production performance.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
Department of Chemistry, The University of Hong Kong, Hong Kong 999077, P. R. China.
Electron donor-acceptor complexes are commonly employed to facilitate photoinduced radical-mediated organic reactions. However, achieving these photochemical processes with catalytic amounts of donors or acceptors can be challenging, especially when aiming to reduce catalyst loadings. Herein, we have unveiled a framework-based heterogenization approach that significantly enhances the photoredox activity of perylene diimide species in radical addition reactions with alkyl silicates by promoting faster and more efficient electron donor-acceptor complex formation.
View Article and Find Full Text PDFChemistry
January 2025
National & Kapodistrian University of Athens, Chemistry, Panepistimiopolis, Zografou, 15771, Athens, GREECE.
The prominence of binuclear catalysts underlines the need for the design and development of diverse bifunctional ligand frameworks that exhibit tunable electronic and structural properties. Such strategies enable metal-metal and ligand-metal cooperation towards catalytic applications, improve catalytic activity, and are essential for advancing multi-electron transfers for catalytic application. Hereby, we present the synthesis, crystal structure, and photocatalytic properties of a binuclear Ni(II) complex, [Ni2(1,10-phenanthroline)2(2-sulfidophenolate)2] (1), which crystallizes in the centrosymmetric triclinic system (P-1) showing extensive intra- and inter- non-coordinated interactions.
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