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Sodium superionic conductor (NASICON)-type Na V (PO ) has attracted considerable interest owing to its stable three-dimensional framework and high operating voltage; however, it suffers from a low-energy density due to the poor intrinsic electronic conductivity and limited redox couples. Herein, the partial substitution of Mn for V in Na V (PO ) is proposed to activate V /V redox couple for boosting energy density of the cathodes (Na V Mn (PO ) ). With the introduction of Mn into Na V (PO ) , the band gap is significantly reduced by 1.406 eV and thus the electronic conductivity is greatly enhanced. The successive conversions of four stable oxidation states (V /V , V /V , and V /V ) are also successfully achieved in the voltage window of 1.4-4.0 V, corresponding to three electrons involved in the reversible reaction. Consequently, the cathode with x = 0.5 exhibits a high reversible discharge capacity of 170.9 mAh g at 0.5 C with an ultrahigh energy density of 577 Wh kg . Ex-situ x-ray diffraction (XRD) analysis reveals that the sodium-storage mechanism for Mn-doped Na V (PO ) consists of single-phase and bi-phase reactions. This work deepens the understanding of the activation of reversible three-electron reaction in NASICON-structured polyanionic phosphates and provides a feasible strategy to develop high-energy-density cathodes for sodium-ion batteries.
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http://dx.doi.org/10.1002/smll.202304002 | DOI Listing |
Anal Chem
September 2025
Institute for Advanced Interdisciplinary Research (iAIR), School of Chemistry and Chemical Engineering, University of Jinan, Jinan 250022, P. R. China.
Compared with efficient anodic luminol electrochemiluminescence (ECL), the disadvantage of cathodic ECL is that luminol cannot be electrochemically oxidized in a direct manner, and the conversion efficiency of dissolved oxygen (DO) as the coreactant to reactive oxygen species (ROS) is poor, which limits its application. Therefore, it is necessary to develop a functional catalyst suitable for the luminol-DO ECL system to directly trigger cathodic ECL. In this study, a coordination microenvironment modulation strategy was proposed.
View Article and Find Full Text PDFInorg Chem
April 2025
School of Chemical Sciences, University of Chinese Academy of Sciences, Beijing 100049, P. R. China.
Nitrogen fixation catalyzed by transition metal complexes provides an attractive alternative to the Haber-Bosch process and has received widespread attention. In this work, the reaction pathways of N to NH/NH catalyzed by dinuclear and mononuclear Cr-N complexes bearing cyclopentadienyl-phosphine ligands and mediated by LutH (as proton donors) and CrCp* (as electron donors) were investigated systematically using density functional theory calculations. The key step of the reactions was clarified as the first hydrogenation.
View Article and Find Full Text PDFChemistry
May 2025
Institut für Anorganische und Analytische Chemie, Technische Universität Braunschweig, Hagenring 30, 38106, Braunschweig, Germany.
The reaction of manganese pentacarbonyl bromide with the N-heterocyclic carbene-phosphinidene adduct (IDipp)PSiMe afforded the tetracarbonyl complex [(IDipp)PMn(CO)] (1) with the release of MeSiBr and CO (IDipp = 1,3-bis(2,6-diisopropylphenyl)-imidazolin-2-ylidene). X-ray crystallographic analysis revealed a trigonal-bipyramidal coordination geometry with a short Mn─P bond, indicative of double bond character. CO substitution with phosphines, NHCs, and isocyanides yielded complexes [(IDipp)PMnL(CO)] (2-5) in which the ligands (L) occupy axial positions.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
May 2025
Department of Chemistry, University of Puerto Rico-Rio Piedras Campus, San Juan, PR, 00925, USA.
Aqueous trivalent metal batteries are promising energy storage systems, which can leverage unique three-electron redox reactions to deliver high capacity and high energy. Among them, antimony (Sb) stands out with a high capacity (660 mAh g), abundant availability, and low cost. However, the severe Sb hydrolysis reaction drastically hinders the development of aqueous antimony batteries.
View Article and Find Full Text PDFSmall
March 2025
Department of Materials Science and Engineering, Department of Chemistry, Hong Kong Institute of Clean Energy (HKICE) & Center of Super-Diamond and Advanced Films (COSDAF), City University of Hong Kong, Hong Kong SAR, 999077, China.
By modifying the coordination environment of single-Fe-atom active site, effective regulation of the photocatalytic oxygen reduction pathway can be achieved to attain high activity for photocatalytic oxidation of CH to CHOH in an aqueous solution. A comprehensive investigation is conducted to study the impact of different coordination numbers of single Fe atoms on photocatalytic CH oxidation reaction over carbon nitride. Among which, Fe/CN with a Fe-N3 coordination exhibit an exceptional photocatalytic performance in CH oxidation, reaching a remarkable methanol yield of 928.
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