Naveed Ahmad, Li Teng, Ali Amjad, Ahmad Farooq, Qureshi Waqar Ahmad, Su Mingru, Li Xiaowei, Zhou Yu, Wu Jian-Chun, Liu Yunjian
School of Material Science and Engineering, Jiangsu University, Zhenjiang, 212013, China.
School of Water, Energy and Environment, Cranfield University, Bedfordshire, MK43 0AL, UK.
Small. 2024 Oct;20(40):e2401589. doi: 10.1002/smll.202401589. Epub 2024 Apr 3.
Despite possessing substantial benefits of enhanced safety and cost-effectiveness, the aqueous zinc ion batteries (AZIBs) still suffers with the critical challenges induced by inherent instability of Zn metal in aqueous electrolytes. Zn dendrites, surface passivation, and corrosion are some of the key challenges governed by water-driven side reactions in Zn anodes. Herein, a highly reversible Zn anode is demonstrated via interfacial engineering of Zn/electrolyte driven by amino acid D-Phenylalanine (DPA) additions. The preferential adsorption of DPA and the development of compact SEI on the Zn anode suppressed the side reactions, leading to controlled and uniform Zn deposition. As a result, DPA added aqueous electrolyte stabilized Zn anode under severe test environments of 20.0 mA cm and 10.0 mAh cm along with an average plating/stripping Coulombic efficiency of 99.37%. Under multiple testing conditions, the DPA-incorporated electrolyte outperforms the control group electrolyte, revealing the critical additive impact on Zn anode stability. This study advances interfacial engineering through versatile electrolyte additive(s) toward development of stable Zn anode, which may lead to its practical implementation in aqueous rechargeable zinc batteries.
尽管水系锌离子电池(AZIBs)具有提高安全性和成本效益等诸多优点,但由于锌金属在水系电解质中固有的不稳定性,仍面临严峻挑战。锌枝晶、表面钝化和腐蚀是锌负极中由水驱动的副反应所导致的一些关键挑战。在此,通过添加氨基酸D-苯丙氨酸(DPA)驱动的锌/电解质界面工程,展示了一种高度可逆的锌负极。DPA在锌负极上的优先吸附以及致密固体电解质界面(SEI)的形成抑制了副反应,导致锌的沉积可控且均匀。结果,添加DPA的水系电解质在20.0 mA cm和10.0 mAh cm的严苛测试环境下稳定了锌负极,平均电镀/剥离库仑效率为99.37%。在多种测试条件下,添加DPA的电解质优于对照组电解质,揭示了添加剂对锌负极稳定性的关键影响。本研究通过通用的电解质添加剂推进界面工程,以开发稳定的锌负极,这可能使其在水系可充电锌电池中得到实际应用。