Yin Hongting, Wu Hao, Yang Yu, Yao Shun, Han Peng, Shi Yiliang, Liu Ruiping
School of Chemical & Environmental Engineering, China University of Mining and Technology (Beijing), Beijing, 100083, P. R. China.
Small. 2024 Dec;20(50):e2404367. doi: 10.1002/smll.202404367. Epub 2024 Sep 30.
Aqueous zinc-ion batteries (AZIBs) stand out among new energy storage devices due to their excellent safety and environmental friendliness. However, the formation of dendrites and side reactions on the zinc metal anode during cycling have become the major obstacles to their commercialization. This study innovatively selected Sodium 4-vinylbenzenesulfonate (VBS) as a multifunctional electrolyte additive to address the issues. The dissociated VBS- anions can not only significantly alter the hydrogen bond network structure of HO in the electrolyte, but also preferentially adsorb on the surface of the zinc anode before HO molecules, which will result in the development of organic anion-rich interface and alterations to the electrical double layer (EDL) structure. Furthermore, the ─C═C─ structure in VBS leads to the formation of an in situ polymerized organic anion solid electrolyte interface (SEI) layer that adheres to the surface of the zinc anode. The mechanisms work together to significantly improve the performance of Zn//Zn symmetric batteries, achieving a cycle life of over 1800 h at 1 mA cm and 1 mAh cm. The introduction of VBS also enhances the cycling performance and capacity of Zn//δ-MnO full cells. This study provides a low-cost solution for the development of AZIBs.
水系锌离子电池(AZIBs)因其出色的安全性和环境友好性,在新型储能设备中脱颖而出。然而,在循环过程中锌金属阳极上枝晶的形成和副反应已成为其商业化的主要障碍。本研究创新性地选择4-乙烯基苯磺酸钠(VBS)作为多功能电解质添加剂来解决这些问题。解离的VBS阴离子不仅能显著改变电解质中HO的氢键网络结构,还能在HO分子之前优先吸附在锌阳极表面,这将导致富含有机阴离子的界面的形成以及双电层(EDL)结构的改变。此外,VBS中的─C═C─结构导致形成原位聚合的有机阴离子固体电解质界面(SEI)层,该层附着在锌阳极表面。这些机制共同作用,显著提高了Zn//Zn对称电池的性能,在1 mA cm和1 mAh cm条件下实现了超过1800小时的循环寿命。VBS的引入还提高了Zn//δ-MnO全电池的循环性能和容量。本研究为水系锌离子电池的发展提供了一种低成本的解决方案。