Yang Song, Wu Qing, Li Yue, Luo Fusheng, Zhang Jinlong, Chen Kui, You Yang, Huang Jun, Xie Haibo, Chen Yiwang
Department of Polymeric Materials & Engineering, College of Materials & Metallurgy, Guizhou University, Huaxi District, 550025, Guiyang, China.
Institute of Polymers and Energy Chemistry (IPEC)/, Film Energy Chemistry for Jiangxi Provincial Key Laboratory (FEC), Nanchang University, 999 Xuefu Avenue, 330031, Nanchang, China.
Angew Chem Int Ed Engl. 2024 Oct 24;63(44):e202409160. doi: 10.1002/anie.202409160. Epub 2024 Sep 24.
Flexible and high-performance aqueous zinc-ion batteries (ZIBs), coupled with low cost and safe, are considered as one of the most promising energy storage candidates for wearable electronics. Hydrogel electrolytes present a compelling alternative to liquid electrolytes due to their remarkable flexibility and clear advantages in mitigating parasitic side reactions. However, hydrogel electrolytes suffer from poor mechanical properties and interfacial chemistry, which limits them to suppressed performance levels in flexible ZIBs, especially under harsh mechanical strains. Herein, a bio-inspired multifunctional hydrogel electrolyte network (polyacrylamide (PAM)/trehalose) with improved mechanical and adhesive properties was developed via a simple trehalose network-repairing strategy to stabilize the interfacial chemistry for dendrite-free and long-life flexible ZIBs. As a result, the trehalose-modified PAM hydrogel exhibits a superior strength and stretchability up to 100 kPa and 5338 %, respectively, as well as strong adhesive properties to various substrates. Also, the PAM/trehalose hydrogel electrolyte provides superior anti-corrosion capability for Zn anode and regulates Zn nucleation/growth, resulting in achieving a high Coulombic efficiency of 98.8 %, and long-term stability over 2400 h. Importantly, the flexible Zn//MnO pouch cell exhibits excellent cycling performance under different bending conditions, which offers a great potential in flexible energy-related applications and beyond.
柔性且高性能的水系锌离子电池(ZIBs),兼具低成本和安全性,被认为是可穿戴电子产品中最具潜力的储能候选之一。水凝胶电解质因其卓越的柔韧性以及在减轻寄生副反应方面的明显优势,成为液体电解质颇具吸引力的替代品。然而,水凝胶电解质存在机械性能差和界面化学问题,这限制了它们在柔性锌离子电池中的性能水平,尤其是在苛刻的机械应变条件下。在此,通过一种简单的海藻糖网络修复策略,开发了一种具有改善的机械和粘附性能的仿生多功能水凝胶电解质网络(聚丙烯酰胺(PAM)/海藻糖),以稳定界面化学,实现无枝晶且长寿命的柔性锌离子电池。结果,海藻糖改性的PAM水凝胶分别表现出高达100 kPa和5338%的卓越强度和拉伸性,以及对各种基材的强粘附性能。此外,PAM/海藻糖水凝胶电解质为锌阳极提供了卓越的抗腐蚀能力,并调节锌的成核/生长,从而实现了98.8%的高库仑效率以及超过2400小时的长期稳定性。重要的是,柔性锌//MnO软包电池在不同弯曲条件下表现出优异的循环性能,这在柔性能源相关应用及其他领域具有巨大潜力。