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Significant efforts have been devoted to optimizing the morphology and synthesizing composite materials to activate SnO for sodium-ion batteries. However, challenges arising from its intrinsic crystal structure remain insufficiently addressed. This study aims to introduce both oxygen vacancies and fluorine ions into the SnO lattice, yielding a modified compound with a chemical composition of SnO£F. Notably, SnO£F anode exhibits an enhanced discharge capacity and improved cycling stability. These enhancements are attributed to the accelerated Na diffusion and increased electrochemical activity, as confirmed by kinetics investigations and in situ X-ray diffraction (XRD) characterizations. Furthermore, cryogenic transmission electron microscopy (cryo-TEM) analyses reveal that the coexistence of oxygen vacancies and fluorine anions promotes the formation of a NaF-rich solid electrolyte interface (SEI) layer, showing an excellent compatibility in sodium-ion batteries, which holds prospects for the realization of the next generation of energy storage systems.
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http://dx.doi.org/10.1002/smll.202506470 | 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 PDFAngew Chem Int Ed Engl
September 2025
School of Integrated Circuits, State Key Laboratory of New Textile Materials and Advanced Processing, Key Laboratory of Material Chemistry for Energy Conversion and Storage (Ministry of Education), Huazhong University of Science and Technology, Wuhan, 430074, China.
Low-temperature rechargeable batteries face great challenges due to the sluggish reaction kinetics. Redox covalent organic frameworks (COFs) with porous structures provide a viable solution to accelerate the ionic diffusion and reaction kinetics at low temperatures. However, the applications of COFs in low-temperature batteries are still at their infancy stage.
View Article and Find Full Text PDFLangmuir
September 2025
College of Textile and Clothing Engineering, Soochow University, Suzhou 215123, PR China.
Sodium-ion batteries are promising candidates for large-scale energy storage due to their low cost and resource abundance. However, their cathode materials suffer from poor conductivity and limited cycling stability. Here, we report a Prussian blue (PB)-based cathode hybridized with carboxyl-functionalized carbon nanotubes (CNTs) via a glutamic acid-assisted in situ coordination route.
View Article and Find Full Text PDFACS Nano
September 2025
Key Laboratory of Applied Surface and Colloid Chemistry (Ministry of Education), School of Chemistry and Chemical Engineering, Shaanxi Normal University, Xi'an 710119, P. R. China.
Transition metal chalcogenides (TMCs) have garnered significant attention as high-capacity anode materials, yet the unconventional role of the Cu collector meditating atomic-level substitution of metal-site cations by Cu ions during electrochemical cycling remains mechanistically unclear. To address this, herein, Cu-doped MoSe@C ultrathin nanosheets were synthesized via the solvothermal process and carbonization strategies. A systematic investigation was conducted to elucidate the underlying driving forces for Cu substitution at Mo sites and the crucial regulatory effects of solid electrolyte interphase (SEI) formation.
View Article and Find Full Text PDFACS Nano
September 2025
College of Chemistry and Chemical Engineering, Central South University, Changsha 410083, China.
The integration of Mn in NaMnFe(PO)PO (NMFPP) enhances the energy density but compromises the Na mobility and structural stability due to limited electron hopping and pronounced Jahn-Teller effects. To address this, a structurally compatible anionic substitution strategy is implemented by partially replacing PO with bulkier and less electronegative SiO groups. The reinforced cathode exhibits enhanced rate performance, which is attributed to lattice expansion induced by the larger SiO units, thereby facilitating Na diffusion and reducing impedance during charge-discharge processes, as supported by GITT and DRT analyses.
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