Nanofiber-Reinforced Composite Polymer Electrolyte Enables Continuous Lithium-Ion Transport and Anion-Rich Solvation Structure for 670 Wh kg–1 Lithium Batteries

电解质 溶剂化 化学 阴极 复合数 化学工程 电化学 氧化物 阳极 泄漏(经济) 石墨烯 纳米纤维 聚合物 电化学窗口 环氧乙烷 氧化呋咱环 枝晶(数学) 储能 锂(药物) 纳米技术 热传导 介孔材料 溶剂 电极 聚合物电解质 离子电导率 磺酸盐 氧气 吸附
作者
Po Bian,Xingchen Song,Zhaozhong Wang,Jie Zhu,Yutong Ding,Jinping Zhang,Yuhu Li,Yansong Liu,Genglin Lou,Aihong Li,Chenxi Li,Yong Li,Hongtao Zhang,Yongsheng Chen
出处
期刊:Journal of the American Chemical Society [American Chemical Society]
标识
DOI:10.1021/jacs.6c09551
摘要

Abstract Solid-state electrolytes are highly promising for high-energy lithium-metal batteries, yet their practical applications are severely restricted by insufficient oxidative stability, sluggish Li+ transport, and unstable electrode/electrolyte interphases under high-voltage operation. Herein, we report an in situ fabricated composite polymer electrolyte, denoted as LAFE, which integrates a designed main-chain fluorinated polyether matrix with an interconnected three-dimensional framework of Li- and F-codoped hydroxyapatite nanofibers (LANs). Distinct from conventional particle-filled composite electrolytes, the lithium-active LAN framework forms continuous Li+-conducting pathways while simultaneously providing abundant interfacial migration sites through strong Li+–LAN interactions, coupling bulk conduction with site-mediated Li+ hopping. The Li+-affinity contrast between LANs and the fluorinated polyether further induces heterogeneous Li-rich and Li-deficient domains, reconstructing the local solvation environment toward an anion-rich structure. This solvation regulation expands the electrochemical stability window to 3.0–5.7 V and promotes preferential anion-derived inorganic-rich LiF/Li3N/B–O-containing SEI and CEI layers, thereby suppressing Li dendrite growth, electrolyte oxidation, and high-voltage cathode degradation while strengthening abuse tolerance by immobilizing the electrolyte within a solidified framework. Consequently, LAFE enables Li||LiNi0.8Co0.1Mn0.1O2 cells to operate stably for 1000 cycles under 4.5–4.7 V and 5 C. At the pouch-cell level, 7 Ah Li||LiCoO2 and 10 Ah Li||Li-rich Mn-based oxide cells deliver energy densities of 677 Wh kg–1 and 632 Wh kg–1, respectively, while 5 Ah Li|| Ni0.8Co0.1Mn0.1O2 pouch cells pass nail penetration without leakage or combustion. This work establishes a lithium-active composite-electrolyte design principle for high-voltage, high-rate, and safe high-energy lithium-metal batteries.
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