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一种有机分子协同策略引入高锌通量固体电解质界面用于稳定水系锌离子电池

A Synergistic Strategy of Organic Molecules Introduced a High Zn Flux Solid Electrolyte Interphase for Stable Aqueous Zinc-Ion Batteries.

作者信息

Wang Nengze, Zhang Yunpeng, Yuan Junyu, Hu Lei, Sun Mengxuan, Li Zhijie, Yao Xiaojun, Weng Xiaolong, Jia Chunyang

机构信息

Shenzhen Institute for Advanced Study, University of Electronic Science and Technology of China, Shenzhen518110, P. R. China.

State Key Laboratory of Electronic Thin Films and Integrated Devices, School of Electronic Science and Engineering, University of Electronic Science and Technology of China, Chengdu610054, P. R. China.

出版信息

ACS Appl Mater Interfaces. 2022 Oct 26;14(42):48081-48090. doi: 10.1021/acsami.2c12118. Epub 2022 Oct 12.

Abstract

Aqueous rechargeable zinc-ion batteries (ARZIBs) are considered as attractive candidates for the next generation of high-safety and low-cost energy storage in large-scale power grids. However, challenges such as the dendrites and the corrosion on the zinc (Zn) surface result in short battery life and low reversibility of Zn plating/stripping. In this work, a method of preconditioning of a zinc anode in hybrid electrolytes (based on poly(ethylene glycol)-200 and HO) to form a solid electrolyte interphase (SEI) that prevents anode corrosion and dendrites is proposed. Though surface composition analysis and density functional theory calculation, this SEI has dense organic and inorganic components due to the induction of organic molecules and anions and has rapid kinetic and high-throughput properties for the transport of zinc ions. As a result, the SEI-modified Zn anode can maintain a low-voltage hysteresis stable cycle for more than 1600 h in aqueous electrolyte. The anode also exhibits impressive reversibility with a high Coulomobic efficiency of 99.23% over 1300 cycles. Furthermore, the ARZIB encapsulated by this anode and Mn-doped VO cathode enables an outstanding electrochemical stability (181.8 mAh g after 800 cycles at room temperature, 102.2 mAh g after 1000 cycles at -15 °C). This work provides an intriguing idea for the stability maintenance of the anode for ARZIBs or other metal-ion batteries.

摘要

水系可充电锌离子电池(ARZIBs)被认为是下一代用于大规模电网的高安全性、低成本储能的极具吸引力的候选者。然而,诸如锌(Zn)表面的枝晶和腐蚀等挑战导致电池寿命短以及锌电镀/剥离的可逆性低。在这项工作中,提出了一种在混合电解质(基于聚乙二醇-200和HO)中对锌阳极进行预处理以形成防止阳极腐蚀和枝晶的固体电解质界面(SEI)的方法。通过表面成分分析和密度泛函理论计算,由于有机分子和阴离子的诱导,该SEI具有致密的有机和无机成分,并且对于锌离子的传输具有快速动力学和高通量特性。结果,经SEI修饰的锌阳极在水系电解质中可保持低电压滞后稳定循环超过1600小时。该阳极在1300次循环中还表现出令人印象深刻的可逆性,库仑效率高达99.23%。此外,由该阳极和锰掺杂的VO阴极封装的ARZIB具有出色的电化学稳定性(室温下800次循环后为181.8 mAh g,-15°C下1000次循环后为102.2 mAh g)。这项工作为ARZIBs或其他金属离子电池阳极的稳定性维持提供了一个有趣的思路。

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