The one-pot synthesis of nanostructured ternary mixed oxides is challenging due to the heterogeneous nature of the hydrolysis and condensation processes of all metal oxide precursors. In addition, the solvents and additives used can affect these processes too. Herein, we report the effect of different solvents (ethanol, 1- and 2-propanol, or butanol) and additives (citric acid or 1,3,5-triisopropylbenzene) used on the formation of binary and ternary alumina-based oxides, NiO-AlO, NiO-TiO-AlO, and NiO-ZrO-AlO in the presence of triblock copolymer Pluronic P123 used as a soft template. For comparison, this study includes also mesoporous AlO prepared at the same conditions. It is shown that the kinetics of hydrolysis and condensation processes of metal alkoxides, and consequently, the properties of the resulting alumina-based mixed metal oxides are controllable by varying the solvents used. The use of propanol instead of ethanol affords mixed metal oxides with improved degree of mesostructure uniformity as evidenced by narrower pore size distributions. This finding is attributed to the smaller exchange of propanol with propoxide groups in Al(OPr), Ti(OPr), and Zr(OPr) which results in an enhanced stability of the formed mesophase. Furthermore, the addition of citric acid leads to smaller pore sizes without significant changes in the textural properties of metal oxides, while addition of 1,3,5-triisopropylbenzene affords oxides with enlarged pores. The mixed metal oxides studied feature large specific surface areas (310-460 m·g), large pore volumes (0.5-0.75 cm·g), and uniform mesopores with widths ranging from 5 to 18 nm. Solid-state kinetic studies performed by thermal analysis using both isoconversional and model fitting methods reveal the complexity of the mesophase formation. The thermal decomposition of condensed oxoalkoxide species into metal oxides is mainly diffusion-controlled and affected by the type of solvent used too. This study shows that there are tremendous opportunities in tailoring porous structures of mixed metal oxides prepared via evaporation induced self-assembly (EISA) by selecting proper solvents and additives, and thermal treatment.
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http://dx.doi.org/10.1016/j.jcis.2018.11.044 | DOI Listing |
Fish Physiol Biochem
January 2025
Department of Biological Sciences, College of Science, University of Jeddah, P.O. Box 80327, Jeddah 21589, Saudi Arabia.
High cadmium (Cd) concentrations pose a threat to aquatic life globally. This study examined the efficiency of adding purslane (Portulaca oleracea L.) leaf powder (PLP) to Oreochromis niloticus diets on Cd's negative effects.
View Article and Find Full Text PDFMikrochim Acta
January 2025
Department of Chemistry, Sardar Vallabhbhai National Institute of Technology, Surat, Gujarat, 395 007, India.
A fluorescence "turn-off-on" nanoprobe is designed by using europium-doped strontium molybdate perovskite quantum dots (Eu:SMO PQDs) for the sequential detection of hypoxanthine (Hx) and Fe. The Eu:SMO PQDs were prepared by the sol-gel method using Sr(NO), (NH)MoO.4HO, and Eu(OCOCH) as precursors.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Institute of Materials Research and Engineering, Sensor and Flexible Electronics, 2 Fusionopolis Way, 138634, SINGAPORE.
Radical covalent organic frameworks (RCOFs) have demonstrated significant potential in redox catalysis and energy conversion applications. However, the synthesis of stable RCOFs with well-defined neutral carbon radical centers is challenging due to the inherent radical instability, limited synthetic methods and characterization difficulties. Building upon the understanding of stable carbon radicals and structural modulations for preparing crystalline COFs, herein we report the synthesis of a crystalline carbon-centered RCOF through a facile post-oxidation process.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Key Laboratory of Carbon Materials of Zhejiang Province, Wenzhou University, Wenzhou 325035, China.
Developing high-energy-density lithium-sulfur batteries faces serious polysulfide shuttle effects and sluggish conversion kinetics, often necessitating the excessive use of electrolytes, which in turn adversely affects battery performance. Our study introduces a meticulously designed electrocatalyst, Cu-CeO@N/C, to enhance lean-electrolyte lithium-sulfur battery performance. This catalyst, featuring in situ synthesized Cu clusters, regulates oxygen vacancies in CeO and forms Cu-CeO heterojunctions, thereby diminishing sulfur conversion barriers and hastening reaction kinetics through the generation of S/S intermediates.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Research Center of Resource Chemistry and Energy Materials, Key Laboratory of Clay Mineral of Gansu, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou 730000, P.R. China.
Clay minerals show significant potential as fillers in polymer composite solid electrolytes (CSEs), whereas the influence of their microstructures on lithium-ion (Li) transport properties remains insufficiently understood. Herein, we design advanced poly(ethylene oxide) (PEO)-based CSEs incorporating clay minerals with diverse microstructures including 1D halloysite nanotubes, 2D Laponite (Lap) nanosheets, and 3D porous diatomite. These minerals form distinct Li transport pathways at the clay-PEO interfaces due to their varied structural configurations.
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