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通过具有受限水的水合共晶电解质诱导缺水界面以实现高性能水系锌金属电池

Water-Deficient Interface Induced via Hydrated Eutectic Electrolyte with Restrictive Water to Achieve High-Performance Aqueous Zinc Metal Batteries.

作者信息

Luo Ping, Wang Yuyuan, Zhang Wenwei, Huang Zhen, Chao Feiyang, Yuan Yuxin, Wang Yipeng, He Yufan, Yu Gongtao, Zhu Dongyao, Wang Zhaoyang, Tang Han, An Qinyou

机构信息

Hubei Provincial Key Laboratory of Green Materials for Light Industry, Hubei Engineering Laboratory of Automotive Lightweight Materials and Processing, School of Materials and Chemical Engineering, Hubei University of Technology, Wuhan, 430068, P. R. China.

Hubei Longzhong Laboratory, Xiangyang, Hubei, 441000, P. R. China.

出版信息

Small. 2025 Mar;21(9):e2410946. doi: 10.1002/smll.202410946. Epub 2025 Jan 23.

Abstract

The development of aqueous zinc metal batteries (AZMBs) is hampered by dendrites and side reactions induced by reactive HO. In this study, a hydrated eutectic electrolyte with restrictive water consisting of zinc trifluoromethanesulfonate (Zn(OTf)), 1,3-propanediol (PDO), and water is developed to improve the stability of the anode/electrolyte interface in AZMBs via the formation of a water-deficient interface. Additionally, PDO participates in the Zn solvation structure and inhibits the movement of water molecules. PDO also preferentially adsorbs along the Zn (100) plane, thereby inducing the formation of the organic/inorganic SEI layer that enables the cycle life of a Zn//Zn symmetric cell to reach 3000 h at 1 mA cm and 1 mAh cm. Further, interfacial modulation by the eutectic electrolyte improves the cycling stability of Zn//VO and Zn//VO cells. Particularly, the specific capacity of a Zn//VO cell with the eutectic electrolyte is 1.7 times that of a cell with the 2M Zn(OTf) electrolyte, with a capacity retention of 93% after 100 cycles at 0.5 A g. This study provides a new perspective on the electrolyte modification strategies for AZMBs, highlighting the potential of PDO-8 electrolyte in developing aqueous energy storage devices with excellent cycling stability.

摘要

水系锌金属电池(AZMBs)的发展受到由活性羟基引发的枝晶和副反应的阻碍。在本研究中,开发了一种由三氟甲磺酸锌(Zn(OTf))、1,3 - 丙二醇(PDO)和水组成的具有限制水的水合共晶电解质,通过形成缺水界面来提高AZMBs中阳极/电解质界面的稳定性。此外,PDO参与锌溶剂化结构并抑制水分子的移动。PDO还优先沿Zn(100)平面吸附,从而诱导形成有机/无机SEI层,使Zn//Zn对称电池在1 mA cm²和1 mAh cm²时的循环寿命达到3000小时。此外,共晶电解质的界面调制提高了Zn//VO₂和Zn//V₂O₅电池的循环稳定性。特别是,采用共晶电解质的Zn//VO₂电池的比容量是采用2M Zn(OTf)电解质的电池的1.7倍,在0.5 A g⁻¹下循环100次后容量保持率为93%。本研究为AZMBs的电解质改性策略提供了新的视角,突出了PDO - 8电解质在开发具有优异循环稳定性的水系储能装置方面的潜力。

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