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Polyethylene terephthalate (PET) tape is widely used by well-known lithium-ion battery manufacturers to prevent electrode stacks from unwinding during assembly. PET tape is selected since it has suitable mechanical and electrical properties, but its chemical stability has been largely overlooked. In the absence of effective electrolyte additives, PET can depolymerize into its monomer dimethyl terephthalate, which is an unwanted redox shuttle that induces substantial self-discharge in a lithium-ion cell. This study presents a chemical screening experiment to probe the PET decomposition mechanism involving in situ generated methanol and lithium methoxide from dimethyl carbonate, one of the most common electrolyte solvents in lithium-ion cells. By screening other polymers, it is found that polypropylene and polyimide (Kapton) are stable in the electrolyte. Finally, it is demonstrated that reversible self-discharge of LiFePO-graphite cells can be virtually eliminated by replacing PET jellyroll tape with chemically stable polypropylene tape.
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http://dx.doi.org/10.1038/s41563-023-01673-3 | DOI Listing |
Small Methods
September 2025
Hebei Key Laboratory of Optic-Electronic Information and Materials, National & Local Joint Engineering Laboratory of New Energy Photoelectric Devices, College of Physics, Science and Technology, Hebei University, Baoding, 071002, China.
As a new generation of high-energy-density energy storage system, solid-state aluminum-ion batteries have attracted much attention. Nowadays polyethylene oxide (PEO)-based electrolytes have been initially applied to Lithium-ion batteries due to their flexible processing and good interfacial compatibility, their application in aluminum-ion batteries still faces problems. To overcome the limitations in aluminum-ion batteries-specifically, strong Al coordination suppressing ion dissociation, high room-temperature crystallinity, and inadequate mechanical strength-this study develops a blended polymer electrolyte (BPE) of polypropylene carbonate (PPC) and PEO.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
Department of Materials Science and Engineering, Norwegian University of Science and Technology, NO-7491 Trondheim, Norway.
LiNiMnO (LNMO) is a promising material for the cathode of lithium-ion batteries (LiBs); however, its high operating voltage causes stability issues when used with carbonate battery electrolytes. Ionic liquids are a viable alternative to conventional carbonate solvents due to their thermal stability and electrochemical window. This work reports the performance of LNMO/Li half cells with an ionic liquid electrolyte (ILE) composed of 0.
View Article and Find Full Text PDFJ Colloid Interface Sci
August 2025
School of Materials Science and Engineering, Harbin Institute of Technology, Shenzhen 518055, PR China; Guangdong Provincial Key Laboratory of Semiconductor Optoelectronic Materials and Intelligent Photonic Systems, School of Materials Science and Engineering, Harbin Institute of Technology, Shenzhe
A critical barrier to commercializing solid-state batteries lies in the inadequate performance of existing solid electrolytes, particularly their poor conductivity at room temperature and unsatisfactory long-term stability. In this context, a self-healing composite solid electrolyte based on succinonitrile (SCN) reinforced with lithium lanthanum titanate (LLTO) is introduced. Leveraging the increased interfacial lithium-ion (Li) transport channels in composite systems, the resultant LLTO-enhanced SCN electrolyte demonstrates remarkable ionic conductivity of 2.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
Department of Chemical Engineering, Shanghai Electrochemical Energy Devices Research Center, School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai, 200240, China.
High-energy lithium-ion batteries necessitate stable Ni-rich layered cathodes, yet critical challenges such as lattice distortion and surface structure collapse remain unresolved. While conventional high-valence doping greatly alleviates surface degradations, it is ineffective in stabilizing bulk lattice due to dopant segregation. Here, we propose a slightly Li-rich (SLR) lattice design by partially substituting transition-metal (TM) ions with Li ions in TM layers, reducing electrostatic repulsion against high-valence dopants.
View Article and Find Full Text PDFACS Omega
August 2025
Institute for Polymers, Composites and Biomaterials (IPCB) U.O.S. of Catania, CNR, Via P. Gaifami 18, 95126 Catania, Italy.
This study explored the potential of blending poly-(ether sulfone)/disulfonated poly-(ether sulfone) (PES/SPES) at various weight ratios with and without polyvinylpyrrolidone (PVP) to enhance the membrane properties for potential applications like fuel cells, water treatment, and lithium-ion battery separators. SPES was appropriately synthesized as a copolymer constituted of alternated unsulfonated (ES) and disulfonated (SES) sequences, achieving a degree of sulfonation of about 100%. SPES improved the membrane's hydrophilicity, while PVP acts as compatibilizer of PES/SPES blends and pore creator.
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