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Rechargeable batteries based on an abundant metal such as aluminum with a three-electron transfer per atom are promising for large-scale electrochemical energy storage. Aluminum can be handled in air, thus offering superior safety, easy fabrication, and low cost. However, the development of Al-ion batteries has been challenging due to the difficulties in identifying suitable cathode materials. This study presents the use of a highly open framework Mo VO as a cathode for Al-ion batteries. The open-tunnel oxide allows a facile diffusion of the guest species and provides sufficient redox centers to help redistribute the charge within the local host lattice during the multivalent-ion insertion, thus leading to good rate capability with a specific capacity among the highest reported in the literature for Al-based batteries. This study also presents the use of Mo VO as a model host to develop a novel ultrafast technique for chemical insertion of Al ions into host structures. The microwave-assisted method employing diethylene glycol and aluminum diacetate (Al(OH)(C H O ) ) can be performed in air in as little as 30 min, which is far superior to the traditional chemical insertion techniques involving moisture-sensitive organometallic reagents. The Al-inserted Al Mo VO obtained by the microwave-assisted chemical insertion can be used in Al-based rechargeable batteries.
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http://dx.doi.org/10.1002/smll.201701296 | DOI Listing |
Langmuir
September 2025
College of Materials and Chemistry & Chemical Engineering, Chengdu University of Technology, Chengdu 610059, PR China.
Hard carbon (HC) has emerged as a promising anode material for sodium-ion batteries (SIBs) owing to its superior sodium storage performance. However, the high cost of conventional HC precursors remains a critical challenge. To address this, coal─a low-cost, carbon-rich precursor─has been explored for HC synthesis.
View Article and Find Full Text PDFOrg Biomol Chem
September 2025
Department of Chemistry, Indian Institute of Technology, Madras, Tamil Nadu, 600036, India.
A synthetic method has been developed for the diastereoselective domino synthesis of indolyl-pyrrolo[2,1-]isoindoles from phthalimide-derived -sulfonyl-1,2,3-triazoles and indoles. The reaction proceeds ring chain isomerization of triazoles to give α-imino diazo compounds. Then, denitrogenative generation of α-imino Rh(II) carbenes followed by intramolecular oxygen insertion and nucleophilic addition of indoles delivers the indolyl-pyrrolo[2,1-]isoindoles.
View Article and Find Full Text PDFChem Commun (Camb)
September 2025
Center for Drug Research and Development, Guangdong Pharmaceutical University, Guangzhou, 510006, P. R. China.
Herein, we report an Ir(III)-catalyzed regioselective C-H acylmethylation of indolizines with β-ketosulfoxonium ylides, enabling the efficient synthesis of C3-functionalized indolizine derivatives. By modifying the reaction conditions, a controllable Ir(III)-catalyzed dicarbonylation of the same substrates was also achieved. In this transformation, β-ketosulfoxonium ylides serve as a rare alternative to conventional oxophenacyl halides.
View Article and Find Full Text PDFInt J Biol Macromol
September 2025
Department of Organic and Inorganic Chemistry, Federal University of Ceará, 60440-900, Fortaleza, CE, Brazil. Electronic address:
Kraft lignin (KL) is a byproduct of the pulp and paper industry and has been extensively used in several high-value-added applications. The aim of this study was to evaluate the potential of phosphorylated Kraft lignins obtained by different reaction conditions (e.g.
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2025
State Key Laboratory of Bio-based Fiber Materials, College of Textile Science and Engineering (International Institute of Silk), Zhejiang Sci-Tech University, Hangzhou 310018, China. Electronic address:
Downsizing Pt particles and incorporating water dissociation site represents a promising strategy for maximizing atomic utilization efficiency and enhancing catalytic performance in Pt-based hydrogen evolution reaction (HER) electrocatalysts. Here, we present a self-supported Pt/Y(OH) electrocatalyst through a synergistic combination of anion insertion-enhanced electrodeposition and chemical deposition at ambient temperature. The resultant architecture features sub-2 nm Pt nanoclusters (with an average diameter of 1.
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