Mingzhu Wu,Feiyu Tao,Yingke Ren,Yifan Wang,Zhaoqian Li,Yang Huang,Li'e Mo,Hong Zhang,Linhua Hu
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引用次数: 0
摘要
开发稳定的水性锌离子电池(AZIBs)需要抑制界面水诱导副反应和锌阳极枝晶生长。电解质添加剂是一种可行的策略,但传统的电解质添加剂通常需要高浓度,这会损害离子电导率,并带来有毒和易燃的问题。在这项工作中,引入微量(0.8 vol%)的聚乙二醇400 (PEG400)作为有效的双电层(EDL)调节器。最小的添加剂负载在不改变整体电解质性质(离子电导率和Zn2+离子溶剂化结构)的情况下,独特地重构了EDL。阐明了一种竞争吸附机制,PEG400具有比H2O更强的吸附能,优先占据Zn阳极表面,形成贫水EDL,抑制水诱导的副反应,提高成核动力学,实现无枝晶沉积。添加PEG400的azib在30 mA cm-2的苛刻测试条件下可实现440小时的卓越循环稳定性,即使在40 mA cm-2的更高电流密度下也可实现180小时的循环稳定性。与nh4v4010 (NVO)阴极耦合的全电池在1 A g-1时提供351 mAh g-1,对应于1000次循环的容量保持率为90%。
Tailoring the Electric Double Layer with Trace PEG400 for Ultra-Stable Zn Anodes.
Developing stable aqueous zinc-ion batteries (AZIBs) requires suppressing interfacial water-induced side reactions and dendrite growth at Zn anodes. Electrolyte additives present a viable strategy, but conventional electrolyte additives often require high concentrations that compromise ionic conductivity and bring about toxic and flammable issues. In this work, trace amounts (0.8 vol%) of polyethylene glycol 400 (PEG400) is introduced to operate as an effective electric double layer (EDL) regulator. The minimal additive loading uniquely restructures the EDL without changing bulk electrolyte properties (ionic conductivity and Zn2+ ions solvation structure). A competitive adsorption mechanism is elucidated, wherein PEG400, possessing stronger adsorption energy than H2O, preferentially occupies the Zn anode surface, forming a H2O-poor EDL that suppresses water-induced side reactions and improves nucleation kinetics to enable dendrite-free deposition. AZIBs with the addition of PEG400 achieve exceptional cycling stability for 440 h under harsh test conditions of 30 mA cm-2 and 180 h even at a higher current density of 40 mA cm-2. Full batteries coupled with NH4V4O10 (NVO) cathodes deliver 351 mAh g-1 at 1 A g-1, corresponding to a capacity retention of 90% for 1000 cycles.
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