Hou Shisheng, Luo Jie, Gong Wenbin, Xie Yucheng, Zhou Xuhui, Yue Fan, Shen Jiaxin, Li Chen, Wei Lei, Xu Feng, Zhang Qichong
Key Laboratory of MEMS of Ministry of Education, School of Integrated Circuits, Southeast University, Nanjing 210096, China.
Key Laboratory of Multifunctional Nanomaterials and Smart Systems, Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences, Suzhou 215123, China.
ACS Nano. 2024 Nov 12;18(45):31524-31536. doi: 10.1021/acsnano.4c12660. Epub 2024 Oct 31.
Aqueous zinc-ion batteries (AZIBs) hold great promise for large-scale energy storage applications, however, their practical use is significantly hindered by issues such as zinc dendrite growth and hydrogen evolution. To address these challenges, we propose a high-entropy (HE) electrolyte design strategy that incorporates multiple zinc salts, aimed at enhancing ion kinetics and improving the electrochemical stability of the electrolyte. The interactions between multiple anions and Zn increase the complexity of the solvation structure, resulting in smaller ion clusters while maintaining weakly anion-rich solvation structures. This leads to improved ion mobility and the formation of robust interphase layers on the electrode-electrolyte interface. Moreover, the HE electrolyte effectively suppresses hydrogen evolution and corrosion side reactions while facilitating uniform and reversible Zn plating/stripping processes. Impressively, the optimized electrolyte enables dendrite-free Zn plating/stripping for over 3000 h in symmetric cells and achieves a high Coulombic efficiency of 99.5% at 10 mA cm in asymmetric cells. Inspiringly, full cells paired with Ca-VO cathodes demonstrate excellent performance, retaining 81.5% of the initial capacity over 1800 cycles at 5 A g. These significant findings highlight the potential of this electrolyte design strategy to improve the performance and lifespan of Zn-metal anodes in AZIBs.
水系锌离子电池(AZIBs)在大规模储能应用方面具有巨大潜力,然而,锌枝晶生长和析氢等问题严重阻碍了它们的实际应用。为应对这些挑战,我们提出了一种包含多种锌盐的高熵(HE)电解质设计策略,旨在增强离子动力学并提高电解质的电化学稳定性。多种阴离子与锌之间的相互作用增加了溶剂化结构的复杂性,导致离子簇更小,同时保持弱富阴离子的溶剂化结构。这导致离子迁移率提高,并在电极 - 电解质界面形成坚固的界面层。此外,高熵电解质有效地抑制了析氢和腐蚀副反应,同时促进了均匀且可逆的锌电镀/剥离过程。令人印象深刻的是,优化后的电解质在对称电池中可实现无枝晶锌电镀/剥离超过3000小时,在非对称电池中10 mA cm下实现了99.5%的高库仑效率。令人鼓舞的是,与Ca-VO阴极配对的全电池表现出优异的性能,在5 A g下1800次循环后仍保留81.5%的初始容量。这些重要发现凸显了这种电解质设计策略在改善水系锌离子电池中锌金属阳极性能和寿命方面的潜力。