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Anode-free sodium metal batteries (AFSMBs) offer a promising solution to enhance the inherently low energy of sodium-ion batteries (SIBs) while circumventing the challenges in processing highly reactive Na metal anodes. However, their practical viability is severely hindered by short lifespan, driven by accelerated irreversible Na loss in zero-Na-excess cell configurations, alongside safety concerns of liquid electrolyte leakage. Here, a design of long-life quasi-solid-state AFSMBs is demonstrated by leveraging polymer regulation of Na solvation behavior and anode interphase chemistry to reduce Na loss while enhancing cell safety. The polyoxymethylene with reduced local steric hindrance and weak Na chelation shapes a weakly solvating polymer-stabilized anion-rich Na solvation structure. It facilitates Na transport and formation of robust inorganic-organic dual-layered solid electrolyte interphase (SEI), enabling smooth Na metal deposition in quasi-solid-state electrolytes. This chemistry yields quasi-solid-state AFSMBs with a long lifespan of 500 cycles and 79% capacity retention at a high rate of 1 C. The 1.2 Ah pouch cells retain 81% capacity over 200 cycles, delivering a volumetric energy of 340 Wh L⁻, surpassing LiFePO||graphite lithium-ion batteries, while achieving a comparable gravimetric energy of 190 Wh kg⁻. Such cells also exhibit high reliability against nail penetration in the open air at a fully charged state.
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http://dx.doi.org/10.1002/adma.202506037 | DOI Listing |
Small
August 2025
Confucius Energy Storage Lab, School of Energy and Environment & Z Energy Storage Center, Southeast University, Nanjing, 211189, China.
Metallic sodium (Na) is an attractive anode material for sodium metal batteries (SMBs) due to its high theoretical capacity and natural abundance. However, the unstable electrolyte/electrode interface and uncontrollable Na dendrite growth arising from the inhomogeneous Na transfer have significantly restricted its practical feasibility. Herein, the topological insulator of bismuth selenide (BiSe), which has protected conducting states on its surface, is selected as a regulator to guide uniform Na transfer.
View Article and Find Full Text PDFChem Commun (Camb)
September 2025
State Key Laboratory of Solidification Processing, Center for Nano Energy Materials, School of Materials Science and Engineering, Northwestern Polytechnical University, Xi'an 710072, P. R. China.
Anode-free batteries promise high energy density but suffer from dendrites, dead sodium, and cathode Na depletion that slow ion diffusion and charge transfer. We introduce the facile chemical pre-sodiation of Cu current collectors to form a NaSn@Cu coating, which enhances Na affinity, supports uniform nucleation, and suppresses dendrites. XRD confirms improved Na diffusion in NaNiMnO, yielding markedly enhanced reversible capacity and cyclability for anode-less sodium-metal batteries.
View Article and Find Full Text PDFAdv Mater
July 2025
Beijing Key Laboratory of Complex Solid State Batteries, Tsinghua Center for Green Chemical Engineering Electrification, State Key Laboratory of Chemical Engineering and Low-Carbon Technology, Department of Chemical Engineering, Tsinghua University, Beijing, 100084, China.
The anode-free strategy enables exceptionally high energy density in rechargeable metal batteries, but the lack of theoretical frameworks impedes current collector design. Here, this study mathematically derives three critical parameters: dielectric coefficient (ɛ), ion mobility (µ_C), and the change of concentration (δC_C), and introduces a quantitative descriptor, k, which serves as a benchmark for evaluating current collector efficiency. Experimentally, a carbon nanotube (CNT)-based current collector is fabricated with minimized ɛ, enhanced δC_C (nano/micro-Sb particles), and µ_C (sodium carboxymethylcellulose, CMC-Na).
View Article and Find Full Text PDFACS Appl Mater Interfaces
August 2025
Department of Physics and Institute of Major Scientific Facilities for New Materials, Southern University of Science and Technology, Shenzhen 518055, China.
Doping with metal ions can significantly enhance the electrochemical performance of NaV(PO) (NVP) as a cathode material for sodium-ion batteries (SIBs). Despite its high reversible capacity and high voltage, practical application of NVP is limited by its poor intrinsic conductivity. Herein, we shed light on a facile sol-gel synthesis method to prepare NVP with ternary doping of potassium K, Al, and SO ions, which accelerates the migration of Na in the crystal structure, as confirmed by theoretical calculations.
View Article and Find Full Text PDFJ Am Chem Soc
July 2025
CAS Key Laboratory of Molecular Nanostructure and Nanotechnology, Beijing National Laboratory for Molecular Sciences (BNLMS), Institute of Chemistry, Chinese Academy of Sciences (CAS), Beijing 100190, P. R. China.
Sufficient active Na and stable electrode-electrolyte interfaces enable anode-free sodium batteries to achieve high energy densities and long operational lifespan. Here, we establish the critical role of low electromotive force (EMF) in promoting uniform Na deposition and stable interfacial chemistry by minimizing overpotential and mitigating steep concentration gradients. We accordingly designed a versatile cathode, Na-replenished P2-type oxides (NRP2), with reversible overstoichiometric Na-ion insertion that incorporates sodium compensation and promotes Na leveling deposition.
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