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揭开奥秘:乙腈与弱溶剂化电解质在塑造锌离子电池气体析出和电化学性能中的相互作用

Unveiling the Mysteries: Acetonitrile's Dance with Weakly-Solvating Electrolytes in Shaping Gas Evolution and Electrochemical Performance of Zinc-ion Batteries.

作者信息

Wu Zhenrui, Li Yihu, Amardeep Amardeep, Shao Yijia, Zhang Yue, Zou Jian, Wang Liping, Xu Jia, Kasprzak Dawid, Hansen Evan J, Liu Jian

机构信息

School of Engineering, Faculty of Applied Science, The University of British Columbia, Kelowna, V1 V 1 V7, Canada.

Department of Physics, Chalmers University of Technology, Göteborg, SE-41296, Sweden.

出版信息

Angew Chem Int Ed Engl. 2024 May 6;63(19):e202402206. doi: 10.1002/anie.202402206. Epub 2024 Apr 5.

DOI:10.1002/anie.202402206
PMID:38457347
Abstract

Aqueous Zn-metal battery (AZMB) is a promising candidate for future large-scale energy storage with commendable capacity, exceptional safety characteristics, and low cost. Acetonitrile (AN) has been widely used as an effective electrolyte constituent to improve AZMBs' performance. However, its functioning mechanisms remain unclear. In this study, we unveiled the critical roles of AN in AZMBs via comparative in situ electrochemical, gaseous, and morphological analyses. Despite its limited ability to solvate Zn ions, AN-modulated Zn-ion solvation sheath with increased anions and decreased water achieves a weakly-solvating electrolyte. As a result, the Zn||Zn cell with AN addition exhibited 63 times longer cycle life than cell without AN and achieved a 4 Ah cm accumulated capacity with no H generation. In VO||Zn cells, for the first time, AN suppressing CO generation, elevating CO-initiation voltage from 2→2.44 V (H: 2.43→2.55 V) was discovered. AN-impeded transit and Zn-side deposition of dissolved vanadium ions, known as "crosstalk," ameliorated inhomogeneous Zn deposition and dendritic Zn growth. At last, we demonstrated an AN-enabled high-areal-capacity AZMB (3.3 mAh cm) using high-mass-loading VO cathode (26 mg cm). This study shed light on the strategy of constructing fast-desolvation electrolytes and offered insights for future electrolyte accommodation for high-voltage AZMB cathodes.

摘要

水系锌金属电池(AZMB)因其容量可观、安全特性卓越且成本低廉,是未来大规模储能的一个有潜力的候选者。乙腈(AN)已被广泛用作一种有效的电解质成分来改善水系锌金属电池的性能。然而,其作用机制仍不清楚。在本研究中,我们通过比较原位电化学、气体和形态分析揭示了乙腈在水系锌金属电池中的关键作用。尽管乙腈溶剂化锌离子的能力有限,但通过增加阴离子和减少水来调节锌离子溶剂化鞘层,乙腈实现了一种弱溶剂化电解质。结果,添加乙腈的锌||锌电池的循环寿命比未添加乙腈的电池长63倍,并且在无氢气产生的情况下实现了4 Ah cm的累积容量。在钒氧化物||锌电池中,首次发现乙腈抑制一氧化碳的产生,将一氧化碳起始电压从2 V提高到2.44 V(氢气:从2.43 V提高到2.55 V)。乙腈阻碍溶解的钒离子的迁移和锌侧沉积,即所谓的“串扰”,改善了不均匀的锌沉积和锌枝晶生长。最后,我们展示了一种使用高质量负载的钒氧化物阴极(26 mg cm)的乙腈基高面积容量水系锌金属电池(3.3 mAh cm)。这项研究揭示了构建快速去溶剂化电解质的策略,并为未来高压水系锌金属电池阴极的电解质适配提供了见解。

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