电解质
钾
电极
离子液体
离子
自行车
材料科学
无机化学
离子键合
化学工程
化学
冶金
有机化学
催化作用
工程类
物理化学
历史
考古
作者
Fei Zhang,Xingchao Wang,Miaomiao Wu,Yong Guo,Yudi Li,Aikai Yang,Jixi Guo,Dianzeng Jia
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2025-07-18
卷期号:10 (8): 3857-3865
被引量:5
标识
DOI:10.1021/acsenergylett.5c01614
摘要
The pursuit of safe high-energy potassium batteries (PBs) encounters critical challenges stemming from unstable interphases at both the anode and cathode and flammable electrolytes. Herein, we engineered a nonflammable ionic liquid (IL) electrolyte that revolutionizes interfacial chemistry through bidirectional anion–cation coordination. This distinctive solvation structure drives the spontaneous formation of inorganic-dominated solid-electrolyte interphase (SEI) and cathode-electrolyte interphase (CEI), enabling dendrite-free K anodes (98.0% Coulomb efficiency over 800 cycles in K//Cu cell, 4800 h ultralong cycling in K//K symmetric cell) and high-voltage Prussian blue cathodes (stable operation at 4.6 V for 2200 cycles). The synergy between FSI – decomposition and PY13 + electrostatic shielding yields an ultrastable graphite//Prussian blue analogue (PBA) full-battery configuration, achieving a record energy density of 148.5 Wh kg –1 with exceptional cyclability exceeding 3600 cycles, outperforming state-of-the-art systems. This work presents a new design concept for nonflammable, long-cycling, high-energy PBs.
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