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Cations Coordination-Regulated Reversibility Enhancement for Aqueous Zn-Ion Battery

机译:水系锌离子电池阳离子协调调节的可逆性增强

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摘要

Aqueous Zn-ion batteries are emerging as a promising candidate for large-scale energy storage, while the short lifetime and poor reversibility of Zn anodes limit their further development. When attempting to enhance reversibility, most reported methods involve toxic and pollutive substances and decreased water content, which inevitably sacrificed safety level, rate performance, and environmentally benign characteristics. Herein, a series of low-cost and "green" molecules are introduced into the aqueous (ZnCl2, ZnSO4) electrolytes, featured with cations coordination capability, which can significantly inhibit the hydration step of Zn2+ and delay the formation of the key by-products (Zn-5(OH)(8)Cl-2 center dot H2O, 3Zn(OH)(3)center dot ZnSO4 center dot 5H(2)O) in aqueous electrolytes via regulating the coordination status of Zn2+. In the optimized electrolyte system, a highly reversible Zn metal anode presents excellent electrochemical performance, featured with a long lifespan over 1185 h at 1 mA cm(-2) and smooth deposition morphology. Furthermore, Zn-MnO2 batteries based on the electrolyte deliver high capacity retention of 82.9 after 200 cycles. These breakthroughs suggest that this method offers a versatile toolbox toward developing future advanced multivalent metal batteries for large-scale energy storage.
机译:水系锌离子电池正在成为大规模储能的有前途的候选者,而锌负极寿命短、可逆性差等特点限制了其进一步发展。在试图提高可逆性时,大多数报道的方法涉及有毒和污染物质以及降低的含水量,这不可避免地牺牲了安全水平、速率性能和环境友好特性。本文将一系列低成本的“绿色”分子引入水电解质(ZnCl2、ZnSO4)中,具有阳离子配位能力,通过调控Zn2+的配位状态,可显著抑制Zn2+的水合步骤,延缓水性电解质中关键副产物(Zn-5(OH)(8)Cl-2中心点H2O、3Zn(OH)(3)中心点ZnSO4中心点5H(2)O)的形成。在优化的电解质体系中,高度可逆的锌金属阳极表现出优异的电化学性能,在1 mA cm(-2)下具有超过1185 h的长寿命和光滑的沉积形貌。此外,基于电解质的 Zn-MnO2 电池在 200 次循环后具有 82.9% 的高容量保持率。这些突破表明,该方法为开发未来用于大规模储能的先进多价金属电池提供了一个多功能的工具箱。

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