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Cluster beam deposition is employed for fabricating well-defined bimetallic plasmonic photocatalysts to enhance their activity while facilitating a more fundamental understanding of their properties. AuAg clusters with compositions ( = 0, 0.1, 0.3, 0.5, 0.7, 0.9 and 1) spanning the metals' miscibility range were produced in the gas-phase and soft-landed on TiO P25-coated silicon wafers with an optimal coverage of 4 atomic monolayer equivalents. Electron microscopy images show that at this coverage most clusters remain well dispersed whereas EXAFS data are in agreement with the finding that the deposited clusters have an average size of . 5 nm and feature the same composition as the ablated alloy targets. A composition-dependant electron transfer from Au to Ag that is likely to impart chemical stability to the bimetallic clusters and protect Ag atoms against oxidation is additionally evidenced by XPS and XANES. Under simulated solar light, AuAg clusters show a remarkable composition-dependent volcano-type enhancement of their photocatalytic activity towards degradation of stearic acid, a model compound for organic fouling on surfaces. The Formal Quantum Efficiency (FQE) is peaking at the AuAg composition with a value that is twice as high as that of the pristine TiO P25 under solar simulator. Under UV the FQE of all compositions remains similar to that of pristine TiO. A classical electromagnetic simulation study confirms that among all compositions AuAg features the largest near-field enhancement in the wavelength range of maximal solar light intensity, as well as sufficient individual photon energy resulting in a better photocatalytic self-cleaning activity. This allows ascribing the mechanism for photocatalysis mostly to the plasmonic effect of the bimetallic clusters through direct electron injection and near-field enhancement from the resonant cluster towards the conduction band of TiO. These results not only demonstrate the added value of using well-defined bimetallic nanocatalysts to enhance their photocatalytic activity but also highlights the potential of the cluster beam deposition to design tailored noble metal modified photocatalytic surfaces with controlled compositions and sizes without involving potentially hazardous chemical agents.
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http://dx.doi.org/10.1039/d2nr07287d | DOI Listing |
Org Lett
September 2025
School of Chemical Sciences, National Institute of Science Education and Research, An OCC of Homi Bhabha National Institute, Bhubaneswar 752050, India.
Selective reduction of heteroaromatic compounds to partially hydrogenated, dearomatized molecules is a tantalizing task. A well-defined, air stable, and pyridine-based Cu(II) NNN pincer complex is developed, which catalyzes selective 1,2-reduction of quinolines. The unstable 1,2-hydrogenated quinolines are transformed into the corresponding amides and isolated in good yields.
View Article and Find Full Text PDFJACS Au
August 2025
Department of Chemistry, Princeton University, Princeton, New Jersey 08544, United States.
Oxidation of the Chatt-type tungsten dinitrogen compound, -(depe)W-(N) (depe = EtPCHCHPEt), with [(η-CH)Fe]-[BAr ] (BAr = B-(3,5-(CF)CH)) resulted in isolation of [(depe)WN]-[BAr ], a rare example of a tungsten-(IV) nitride prepared from N cleavage. A bimetallic μ-N ditungsten intermediate supported by terminal N ligands was identified, and irradiation with visible light promoted dinitrogen cleavage and formation of [(depe)WN]-[BAr ]. Performing the analogous one-electron oxidation of the related tungsten dinitrogen compound, -(dppe)W-(N) (dppe = PhPCHCHPPh), furnished the corresponding cationic, 17-electron tungsten dinitrogen complex, [(dppe)W-(N)]-[BAr ], that was characterized by X-ray diffraction and vibrational and EPR spectroscopies.
View Article and Find Full Text PDFPolymers (Basel)
August 2025
School of Chemical and Materials Engineering (SCME), National University of Sciences and Technology (NUST), Islamabad 44000, Pakistan.
Cu-BTC (HKUST-1) metal-organic framework (MOF) is widely recognized for its carbon capture capability due to its unsaturated copper sites, high surface area, and well-defined porous structure. This study developed mixed matrix membranes (MMMs) using cellulose triacetate (CTA), incorporating bimetallic Ni-Cu-BTC MOFs for CO/CH separation, and benchmarked them against membranes fabricated with monometallic Cu-BTC. CTA was selected for its biodegradability, membrane-forming properties, and cost-effectiveness.
View Article and Find Full Text PDFDalton Trans
August 2025
Department of Molecular Science and Technology, Ajou University, 206 Worldcup-ro, Yeongtong-gu, Suwon 16499, Republic of Korea.
Double metal cyanide complex (DMC) catalysts, widely used industrially for the ring-opening polymerization (ROP) of propylene oxide (PO), have garnered attention for PO/CO copolymerization due to their ease of preparation and high catalytic activity, although their ability to incorporate CO remains relatively limited. In this study, we report DMC variants with well-defined compositions, specifically incorporating ZnOAc and ZnOBu components. These catalysts were synthesized a distinct route from conventional DMCs by reacting KCo(CN) with 2 eq.
View Article and Find Full Text PDFMikrochim Acta
August 2025
Key Laboratory of the Ministry of Education for Advanced Catalysis Materials, College of Chemistry and Materials Science, College of Geography and Environmental Sciences, Zhejiang Normal University, Jinhua, 321004, China.
A colorimetric/fluorescent dual-mode sensor has been developed based on well-dispersed PtMn alloy/porous N-doped carbon nanoflowers (PtMn/CNFs), which have bifunctional ascorbate oxidase (AAO) and peroxidase (POD)-like activities. Specifically, the POD-like activity of PtMn/CNFs enables colorimetric ascorbic acid (AA) detection by oxidizing 3,3',5,5'-tetramethylbenzidine (TMB) to a blue product, while the AAO-like activity facilitates fluorescent detection of AA by catalyzing its oxidation to dehydroascorbic acid (DHA), which subsequently reacts with o-phenylenediamine (OPD) to generate a fluorescent product. The sensor demonstrates wide linear ranges of 2 to 250 µM (detection limit: 0.
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