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Achieving stable cyclability in initially anode-free all-solid-state batteries is challenging due to non-uniform Li (de)plating, especially under practical operating conditions. Here, we introduce a bilayer comprising a silver(Ag)-doped Li-argyrodite electrolyte layer in contact with the undoped Li-argyrodite electrolyte. During charging, electrochemical exsolution of Ag from the silver-doped Li argyrodite forms nanoscale, lithiophilic silver seeds along grain boundaries and in pores where they are accessible for electron transfer. These silver seeds alloy with Li to induce uniform Li plating underneath and return to the electrolyte layer upon Li stripping to enhance the reversibility during cycling. With silver exsolution, a pouch-type full-cell with a volumetric energy density of 1312 Wh L (excluding the packaging materials) and areal discharge capacity of 7.0 mAh cm at 0.7 mA cm, demonstrated stable cycling at a practical stack pressure of 2.0 MPa. This study highlights that Ag diffusion in the Li-argyrodite solid electrolyte and its electrochemical exsolution are an effective strategy for robust, high-energy-density initially anode-free all-solid-state batteries.
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http://dx.doi.org/10.1038/s41467-025-61074-9 | DOI Listing |
Nat Commun
August 2025
Helmholtz-Institute Münster, IMD-4, Forschungszentrum Jülich GmbH, Münster, Germany.
Alloying coatings are widely accepted to boost the reversibility of lithium inventory in anode-free cell configurations. While diminished capacity losses are evident from electrochemical data, their impact beyond decreasing the nucleation overpotential remains elusive. Herein, in situ Li NMR spectroscopy is applied to differentiate capacity losses in pouch cells with representative electrochemical behavior.
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.
View Article and Find Full Text PDFNat Commun
July 2025
School of Chemical and Biological Engineering and Institute of Chemical Processes, Seoul National University, Seoul, Republic of Korea.
Achieving stable cyclability in initially anode-free all-solid-state batteries is challenging due to non-uniform Li (de)plating, especially under practical operating conditions. Here, we introduce a bilayer comprising a silver(Ag)-doped Li-argyrodite electrolyte layer in contact with the undoped Li-argyrodite electrolyte. During charging, electrochemical exsolution of Ag from the silver-doped Li argyrodite forms nanoscale, lithiophilic silver seeds along grain boundaries and in pores where they are accessible for electron transfer.
View Article and Find Full Text PDFACS Appl Mater Interfaces
July 2025
Department of Materials, University of Oxford, Parks Road, Oxford OX1 3PH, U.K.
Solid-state batteries can outperform lithium-ion batteries in energy per unit mass or volume when operating with a Li metal anode. However, Li anodes pose significant manufacturing challenges. Anode-free cells avoid these challenges by plating metallic Li at the anode on the first charge, but subsequent nonuniform cyclic stripping and plating decrease the Coulombic efficiency and encourage Li dendrites and early cell failure.
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