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• W4310235051 abstract "High interfacial energy Li0-electrolyte interface contributes to larger Li0 nucleation embryos and a more stable interface, so the interfacial energy is essential for highly reversible Li0 deposition/stripping. Herein, a high interfacial-energy artificial solid electrolyte interphase (SEI) with rich LiF embedded in lithiated poly-2-acrylamido-2-methylpropane sulfonic acid (PAMPS-Li) network is designed to realize favorable Li0 nucleation and rapid desolvation of Li+ simultaneously. The Li-F bonds in LiF (001) exhibit stronger ion-dipole interactions with Li atoms, offering higher interfacial energies. When the growth surface energy and total interfacial energy of Li0 are balanced, the high interfacial energy SEI with abundant LiF can promote the formation of larger Li0 nucleation embryos. In addition, the PAMPS-Li with immobilized anions presents weaker interaction with Li0 and possesses higher polymer-Li interfacial energy, and its amide and sulfonic acid groups exhibit higher binding energies with Li+. Therefore, PAMPS-Li can easily promote the Li+ to escape from the solvent sheath and weaken the desolvation energy barrier. The highly reversible Li0 deposition behavior with restricted side reactions is achieved based on the synergistic modification of high interfacial energy SEI with heterostructure. Most importantly, lifespan of multi-layered Li0 pouch cell (330 Wh kg-1) with a low N/P ratio (1.67) is over 100 cycles, verifying its potential practical application." @default.
• W4310235051 created "2022-11-30" @default.
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• W4310235051 date "2022-12-01" @default.
• W4310235051 modified "2023-09-25" @default.
• W4310235051 title "High interfacial-energy heterostructure facilitates large-sized lithium nucleation and rapid Li+ desolvation process" @default.
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• W4310235051 doi "https://doi.org/10.1016/j.scib.2022.11.026" @default.
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