Heterojunctions of small CuO nanoclusters (synthesized by radiolysis) with TiO (commercial P25) induced a photocatalytic activity under visible light irradiation in a wide range of wavelengths due to the narrow bandgap of CuO nanoclusters of around 1.7 eV. The optical, chemical, and electrical properties of these composite nanomaterials were studied. The photocatalytic properties of bare and modified TiO-P25 were studied for water purification (photooxidation of organic compounds such as phenol and 2-propanol) and for hydrogen generation under visible light irradiation. Time resolved microwave conductivity signals showed activation of TiO under visible light, proving the injection of electrons from CuO nanoclusters to the conduction band of TiO-P25. The modified materials showed high photocatalytic activity under visible light. The important role of charge-carriers was demonstrated for both photoreduction and photooxidation reactions.
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http://dx.doi.org/10.1063/5.0015277 | DOI Listing |
Angew Chem Int Ed Engl
December 2024
Engineering Research Center of Photoenergy Utilization for Pollution Control and Carbon Reduction of Ministry of Education, College of Chemistry, Central China Normal University, Wuhan, 430079, P. R. China.
Direct electrooxidation of propylene using water-oxidation intermediates represents a promising route for propylene glycol production. Unfortunately, this economic and environmentally friendly process suffers from low yield and poor Faradaic efficiency resulting from the mismatched oxidative capacity of reactive oxygen species and pronounced side reactions. Herein, we developed an earth-abundant metal-based nanocluster CuO-modified MnO catalyst for the efficient electrooxidation of propylene into propylene glycol, achieving a remarkable production rate of 63.
View Article and Find Full Text PDFNanoscale
January 2025
Quantum Solid-State Physics, Department of Physics and Astronomy, KU Leuven, Belgium.
The photoelectrochemical (PEC) water splitting reaction of bimetallic AuCu ( = 1, 0.75, 0.5, 0.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
November 2024
Institute of Molecular Metrology, College of Chemistry and Chemical Engineering, Qingdao University, 266071, Qingdao, China.
The electrochemical conversion of CO into valuable chemicals is a promising route for renowable energy storage and the mitigation of greenhouse gas emission, and production of multicarbon (C) products is highly desired. Here, we report a 1.4 %Pd-Cu@CuPz comprising of dispersive CuO and PdO dual nanoclusters embedded in the MOF CuPz (Pz=Pyrazole), which achieves a high C Faradaic efficiency (FE) of 81.
View Article and Find Full Text PDFAdv Sci (Weinh)
June 2024
School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou, Jiangsu, 225009, P. R. China.
Electrochemical activation usually accompanies in situ atom rearrangement forming new catalytic sites with higher activity due to reconstructed atomic clusters or amorphous phases with abundant dangling bonds, vacancies, and defects. By harnessing the pre-catalytic process of reconstruction, a multilevel structure of CuNi alloy nanoparticles encapsulated in N-doped carbon (CuNi nanoalloy@N/C) transforms into a highly active compound of Ni-doped CuO nanocluster supported on (N/O-C) co-doped C. Both the exposure of accessible active sites and the activity of individual active sites are greatly improved after the pre-catalytic reconstruction.
View Article and Find Full Text PDFInorg Chem
March 2024
Xi'an Key Laboratory of Sustainable Energy Materials Chemistry, College of Chemistry, Xi'an Jiaotong University, Xi'an 710049, P. R. China.
The immobilization of tiny active species within inert mesoporous silica imparts a range of functions, enhancing their applicability. A significant obstacle is the spontaneous migration and aggregation of these species within the mesopores, which threaten their uniform distribution. To address this, we propose a postmodification method that involves grafting transition metal oxide nanoclusters into silica mesopores via interfacial condensation, catalyzed by acetate ions.
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