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Rapid inactive lithium accumulation and severe lithium dendrite growth critically limit the cycle life of metallic lithium anodes. Herein, cyclic thioether 1,3-dithiane is reported as a novel electrolyte additive for fabricating ultra-stable lithium-metal batteries. Through the preferential decomposition of 1,3-dithiane additive and PF anion ions, robust inorganic-rich electrode interphases could be generated at both the anode and the cathode, which is conducive to enhanced kinetics and structural stability of the electrode interface, endowing alleviated active lithium loss and dendrite-free lithium deposition. Moreover, 1,3-dithiane would react with lithium alkylide to reduce the organic component in solid-electrolyte interphases and improve the ability of solvents to resist nucleophilic attack. Consequently, the assembled Li//LiFePO full cells with 2.0 wt% of the 1,3-dithiane-containing electrolyte exhibit a significantly improved capacity retention of 83.6% after 3300 cycles at a current rate of 1.0 C, which highlights that the 1,3-dithiane additive could induce a long-lifespan lithium-metal battery.
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http://dx.doi.org/10.1093/nsr/nwaf259 | DOI Listing |
Angew Chem Int Ed Engl
September 2025
School of Chemistry, Engineering Research Center of Energy Storage Materials and Devices, Ministry of Education, National Innovation Platform (Center) for Industry-Education Integration of Energy Storage Technology, State Key Laboratory of Electrical Insulation and Power Equipment, Engineering Resea
Lithium metal batteries (LMBs) offer exceptional energy density and output voltage. However, their practical application remains hindered by sluggish ion transport and uncontrolled lithium dendrite formation, particularly under fast-charging conditions. Here, we report a facet-engineered anion-regulating separator based on zeolitic imidazolate framework-8 (ZIF-8) with preferentially crystal-exposed (110) facets.
View Article and Find Full Text PDFNatl Sci Rev
August 2025
Confucius Energy Storage Lab, School of Energy and Environment & Z Energy Storage Center, Southeast University, Nanjing 211189, China.
Rapid inactive lithium accumulation and severe lithium dendrite growth critically limit the cycle life of metallic lithium anodes. Herein, cyclic thioether 1,3-dithiane is reported as a novel electrolyte additive for fabricating ultra-stable lithium-metal batteries. Through the preferential decomposition of 1,3-dithiane additive and PF anion ions, robust inorganic-rich electrode interphases could be generated at both the anode and the cathode, which is conducive to enhanced kinetics and structural stability of the electrode interface, endowing alleviated active lithium loss and dendrite-free lithium deposition.
View Article and Find Full Text PDFSmall
August 2025
Institute for Advanced Materials and Technology, University of Science and Technology Beijing, Beijing, 100083, China.
Composite solid-state polymer electrolytes (CPEs) have become a key driving force for the industrialization of solid-state batteries (SSBs) by virtue of their excellent flexibility and processability. Nevertheless, the ionic conduction relaxation of the polymer chain segments leads to localized ion stacking, non-steady state mass transfer, and concentration polarization issues, limiting the further application of CPEs. Herein, a heterogeneous surface is used to modulate the ionic environment of the dispersed phase in CPEs by incorporating high dielectric material BaTiO and LiLaZrTaO (LLZTO) into a flexible crosslinked polyester matrix.
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2025
School of Materials and Energy, University of Electronic Science and Technology of China, Chengdu 611731 Sichuan, China; Yangtze Delta Region Institute (HuZhou), University of Electronic Science and Technology of China, Huzhou 313001 Zhejiang, China. Electronic address:
The unstable interfacial contact and slow Li transport at the side of cathode have been two major challenges for practical application of garnet-based solid-state batteries (SSBs). In this work, a strategy of metal-ligand coordination induced rapid Li transport kinetics through bidirectional anchoring is proposed to address aforementioned issues by decorating the cathode with LiLaZrTaO (LLZTO) nanoparticles and stabilizing the interface with succinonitrile-based interlayer (SL). The strong metal-ligand coordination of the -CN in SL with the LLZTO solid-state electrolytes and the LiCoO (LCO)@LLZTO composite cathode enables an intimate contact at the atomic scale, constructing bidirectional channels of fast Li transport at the interface.
View Article and Find Full Text PDFAdv Mater
July 2025
Guangdong Provincial Key Laboratory of Fuel Cell Technology, School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou, 510641, China.
Solid polymer electrolytes (SPEs) are regarded as promising candidates that could address the safety concerns associated with liquid electrolytes. Nonetheless, SPEs are still confronting serious lithium dendrite issues, and there is a lack of systematic studies regarding the formation of lithium dendrites within SPEs. Herein, Sand equation is employed to elucidate the determinants of dendrite growth in SPEs, revealing that three factors including the Li transference number, Li diffusion coefficient, and Li concentration are positively correlated with Sand's time (τ) which determine the plating/striping behaviors of Li anode.
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