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Microwave heating provides an efficient method to rapidly heat materials through interaction of microwaves with the media. Here, we demonstrate the rapid synthesis of mesoporous cobalt oxide films through the heating of the silicon substrate by microwaves. A non-sol-gel approach based on cobalt nitrate-citric acid complex cooperative assembly with a poly[methoxy poly(ethylene glycol)methacrylate]--poly(butyl acrylate) (PMPEGMA--PBA) block copolymer was used to fabricate the cobalt oxide through a cobalt carbonate intermediate. The time required to convert cobalt carbonate to cobalt oxide with the full removal of the PMPEGMA--PBA template can be decreased by two orders of magnitude with microwaves in comparison to standard heating in a furnace at 350 °C. At the highest microwave power examined (1500 W), this can be accomplished within 2 s, while >5 min is required at 350 °C in a furnace. At a microwave power of <400 W, there is insufficient energy to induce the transition from carbonate to oxide, but even at only 420 W, the oxide can be formed within 26 s. The rapid heating by the microwaves tends to increase the crystallinity and mean crystal size of the cobalt oxide within the mesoporous films. Despite the growth of larger average crystals, the pore size and porosity tend to be larger when the film is processed using microwaves. Higher microwave power leads to larger average crystals and average pore size. These results suggest that rapid processing to crystallize frameworks in mesoporous materials may allow for highly crystalline frameworks without loss of the templated mesostructure.
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http://dx.doi.org/10.1021/acs.langmuir.9b03138 | DOI Listing |
Dalton Trans
September 2025
School of Education, Can Tho University, 3-2 Road, Can Tho City 900000, Vietnam.
Enhancement of the performance of lithium-ion batteries is a critical strategy for addressing the challenges associated with cost and raw materials. By doping boron (B), aluminum (Al), and aluminum/boron (Al/B) utilizing the sol-gel method, we demonstrate a substantial improvement in the cycling performance of Ni-rich lithium nickel manganese cobalt oxide (NMC) as an electrode. While the initial specific capacitance of the doped samples may be lower than that of the pristine NMC, these samples demonstrate a notable increase in specific capacitance during subsequent cycles, reaching a peak around the 10 cycle and nearing the highest specific capacitance observed in NMC cathodes.
View Article and Find Full Text PDFAnal Chem
September 2025
Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, School of Petrochemical Engineering, Changzhou University, Changzhou, Jiangsu 213164, P. R. China.
Rational design of both mechanistic pathways and material compositions is essential to advance COF-based electrochemiluminescence (ECL) systems. In this study, aggregation-induced emission covalent organic framework (AIE-COF) nanoprobes with excellent ECL performance were developed based on Tb-functionalized covalent organic framework (Tb@A-COF). The Tb@A-COF system demonstrates enhanced ECL performance through synergistic integration of three complementary mechanisms: (1) (4',4',4',4'-(1,2-ethenediylidene)tetrakis [1,1'-biphenyl]-4-carboxaldehyde (ETBC) ligands function as antenna-like sensitizers that amplify luminescence intensity by 14.
View Article and Find Full Text PDFJ Chem Phys
September 2025
Department of Chemical Engineering, National Taiwan University of Science and Technology, Taipei 106, Taiwan.
All-solid-state Li-metal batteries using solid polymer electrolytes (SPEs) in combination with high-voltage cathodes such as lithium nickel manganese cobalt oxide (NMC) promise enhanced battery safety, energy density, and flexibility. However, understanding the oxidative decomposition of SPEs on the cathode surfaces and characterizing the resulting cathode-electrolyte interphase (CEI) remain challenging both experimentally and computationally. This study introduces a new computational protocol based on ab initio molecular dynamics for simulating the decomposition of PEO:LiTFSI SPE on the NMC-811 cathode surface using a combined electron- and Li+-removal simulation approach.
View Article and Find Full Text PDFThe increasing demand for efficient energy conversion and storage systems necessitates the development of high-performance, cost-effective electrode materials. To address this challenge, we employed rotten (eggplant) juice as a precursor for the fabrication of low-cost, earth-abundant, and active electrode materials based on cobalt oxide (CoO) nanostructures. Different volumes of rotten juice (5 mL, 10 mL, 15 mL, and 20 mL) were utilized during the precipitation process to synthesize CoO nanostructures.
View Article and Find Full Text PDFRSC Adv
August 2025
Hubei Province Key Laboratory of Agricultural Waste Resource Utilization, Wuhan Polytechnic University Wuhan 430023 China
AS a low-cost and high-performance catalyst, spinel cobalt oxide (CoO) has two different catalytic active sites (tetrahedral Co and octahedral Co) to drive the activation of peroxymonosulfate (PMS) through Co/Co redox cycle. Tuning Co/Co atomic ratio on the surface of CoO for the construction of a synergy in the Co/Co redox cycle might be an effective way to further boost PMS activation performance of CoO catalyst. Herein, we suggested a metal-doping strategy to regulate Co/Co atomic ratio of CoO by partially substituting Co with inert Mg and formed a series of Mg doped CoO (MCO) catalysts.
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