摘要
The instability of Zn anode resulting from corrosion and dendritic growth remain impeding the development of aqueous zinc-ion batteries (AZIBs). In addition, the desolvation on the Zn surface is sluggish, which hinders the reaction kinetics and fast charge/discharge behavior of AZIBs. Herein, the uniform Zn deposition and fast desolvation are realized by using a hydrophilic fumed nano-silica coating with zinc alginate (Alg) as a functional binder (Alg/SiO2@Zn). Combined theoretical calculation and experimental investigations show the interaction between the H2O in the solvation structure and -OH functional group of SiO2 facilitates the desolvation process. In addition to the Zn2+ guiding effect of Alg, the fast Zn2+ diffusion along SiO2 endows the homogeneous Zn deposition. Consequently, Alg/SiO2@Zn symmetric cell demonstrates exceptional plating/stripping reversibility and excellent long-term cycle life at both 1 and 10 mAh cm−2. A full cell assembled with Alg/SiO2@Zn and NaV3O8·xH2O cathode achieves a high capacity of 129 mAh g−1 at 4 A g−1 over 2650 cycles. Even under −20 °C, the battery maintains a high capacity of 136.5 mAh g−1 at 1 A g−1 after 1000 stable cycles. This study provides a facile strategy to achieve a highly stable Zn anode and gains deep insight into desolvation modulation via surface modification.
源语言 | 英语 |
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期刊 | Advanced Science |
DOI | |
出版状态 | 已接受/待刊 - 2025 |