4.8 Article

Supramolecular Salt-Assisted Quasi-Solid-State Electrolyte Promoting Dual Conductive Interface for High-Energy-Density Lithium Metal Batteries

Journal

ADVANCED ENERGY MATERIALS
Volume -, Issue -, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/aenm.202303020

Keywords

dual conductive interface; lithium metal battery; quasi-state polymer electrolyte; solvated structure; supramolecular salt

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This study investigates the modulation effects of supramolecular LiPAAOB salt and 3D PALC polymer host on enhancing intermolecular interactions and promoting the ordered transport of Li+ ions in quasi-solid-state polymer electrolyte. The synthesized LiPAAOB-assisted GPEs show improved electrochemical stable window and ionic conductivity, effectively inhibiting dendrite growth and electrode corrosion, and demonstrating potential application in constructing flexible high-energy-density batteries.
Ion electrokinetic regulation in gel polymer electrolytes (GPEs) is of great significance in alleviating dendrite growth and electrode corrosion of metallic lithium in lithium metal batteries (LMBs). Herein, a supramolecular LiPAAOB salt-assisted GPEs (3D-DIS-1.25% GPEs) is synthesized to improve the ionic electrodynamics of LMBs. The LiPAAOB conductor salt provides sufficient Li+ ions while simultaneously facilitating LiTFSI dissociation. Theses dissociated Li+ ions can be further anchored firmly by enriched affinitive sites (CO, CO) induced in 3D composite polymer skeleton (PALC). Due to the strong hydrogen-bonding interactions between PALC and LiPAAOB/LiTFSI, a stable coordination structure is thereby constructed in 3D-DIS-1.25% GPEs, which then facilitates Li+ ions to transport rapidly along polymer chains. Consequently, the electrochemical stable window and ionic conductivity of the 3D-DIS-1.25% GPEs are increased to as high as 5.3 V and 1.34 mS cm-1, respectively. The Li+/e- double conducting interfaces in situ formed on Li metal anode and active particles in cathodes can effectively inhibit dendrite growth and electrode corrosion. As a result, both Li||3D-DIS-1.25% GPEs||Li symmetrical battery and flexible 3D-DIS-1.25% GPEs-based pouch cell with high LFP loading operate stably even under folded and curly state, indicating the application possibility of using 3D-DIS-1.25% GPEs in constructing various flexible high-energy-density batteries. The modulating effects of supramolecular LiPAAOB salt and 3D PALC polymer host on enhancing intermolecular interactions and promoting the ordered transport of Li+ ions in quasi-solid-state polymer electrolyte are systematically investigated. Both 3D polymer host and supramolecular LiPAAOB provide enriched affinitive sites that can firmly anchor and direct the transport of dissociated Li+ ions, further forming compact SEI/CEI interface layers.image

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