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Currently, heterostructure engineering is considered an optimization strategy to enhance anode performance for sodium-ion batteries. However, ferric vanadate-based heterostructures are rarely reported due to their rapid nucleation. Furthermore, it is a huge challenge to synthesize carbon-coated heterostructure materials through an efficient strategy. Herein, a strategy is proposed for constructing in situ carbon-encapsulated metal selenide/ferric vanadate heterostructure (FeSe/FeVO@C) nanosheets by a selenization-assisted salt template method for the first time. Density functional theory calculations reveal that a built-in electric field at the heterointerface accelerates electron transfer and induces d-electron delocalization in V atoms, increasing the electronic conductivity. Additionally, the confinement effect of the salt template mediates in situ carbon encapsulation and 2D nanostructure formation, alleviating the volume expansion and ensuring structural stability. The introduction of FeSe generates more active sites and accelerates reaction kinetics. Notably, the as-prepared FeSe/FeVO@C-based anode demonstrates outstanding rate performance, delivering capacities of 423 mAh g at 0.5 A g, 228.1 mAh g at 100 A g, and excellent long-term stability with a capacity of 219.9 mAh g at 40 A g after 5000 cycles. This universal strategy for constructing ferric vanadate-based heterostructures and in situ carbon coating offers a promising pathway for secondary battery systems.
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http://dx.doi.org/10.1002/smll.202505581 | DOI Listing |
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August 2025
College of Chemical Engineering, Xinjiang University, Urumqi, Xinjiang, 830017, P. R. China.
Ru-based catalysts have emerged as promising candidates due to their high catalytic activity, yet issues such as kinetic sluggishness and insufficient stability remain. In this study, a carbon-encapsulated RuNi/Ni heterostructured nanoparticle on coal-based carbon nanofiber (RuNi/Ni@C-CNF) is constructed through an in situ pyrolysis strategy. The strategy achieves the highly dispersed loading of metal nanoparticles while synchronously enabling the catalytic graphitization of carbon nanofibers via precursor impregnation coupled with in situ carbothermal reduction.
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August 2025
School of Chemistry and Chemical Engineering, State Key Lab of Urban Water Resource and Environment, Harbin Institute of Technology, Harbin, 150001, China.
Currently, heterostructure engineering is considered an optimization strategy to enhance anode performance for sodium-ion batteries. However, ferric vanadate-based heterostructures are rarely reported due to their rapid nucleation. Furthermore, it is a huge challenge to synthesize carbon-coated heterostructure materials through an efficient strategy.
View Article and Find Full Text PDFSmall Methods
July 2025
Institute of Circular Economy, College of Materials Science and Engineering, Beijing University of Technology, Beijing, 100124, P. R. China.
Green electrochemical synthesis of 2,5-furandicarboxylic acid (FDCA) from biomass is an essential alternative for the substitution of petroleum-based terephthalic acid. The rational design and application of high-performance electrocatalysts are the key to advance this technique. In this work, mesoporous carbon encapsulated ultrafine ScO nanoparticles are reported as a new, highly efficient and selective electrocatalyst that realizes the concurrent electrochemical oxidation of biomass-derived 5-hydroxymethylfurfural (HMF) to FDCA coupled with hydrogen evolution.
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June 2025
ITQ, Instituto de Tecnología Química, Universitat Politècnica de València (UPV), Av. de los Naranjos S/N, Valencia 46022, Spain.
Reducing CO to CO via the reverse water-gas shift (RWGS) reaction is a promising strategy for carbon capture and utilization (CCU). In this study, tailored magnetic catalysts were designed through the pyrolysis of a Co-based MOF to form well-defined nanoparticles. As a result, carbon-encapsulated cobalt nanoparticles () and palladium-doped cobalt nanoparticles () were synthesized and thoroughly characterized using a variety of techniques, including X-ray absorption and diffraction experiments.
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June 2025
Yusuf Hamied Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge, CB21EW, UK.
Phosphorus-doped carbons provide a balance between the electrochemical stability of graphitic lattices and the high energy density of phosphorus materials when used in lithium and sodium-ion batteries. Herein, a comprehensive ex situ P, Li, and Na solid-state nuclear magnetic resonance analysis of the intercalation mechanism of novel, stable, dual-phase phosphorus-doped, and phosphorus-encapsulated turbostratic graphite microspheres is presented. Results indicate that lithium intercalation occurs through the formation of LiP from white phosphorus trapped within the graphitic layers, with the involvement of lithiated phosphorus atoms within the graphitic lattice.
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