阳极
溶剂化
阴极
电解质
水溶液
电池(电)
电化学
化学工程
离子
锌
化学
无机化学
材料科学
电极
物理化学
有机化学
热力学
功率(物理)
物理
工程类
作者
Xin Shi,Jinhao Xie,Jin Wang,Shilei Xie,Zujin Yang,Xihong Lu
标识
DOI:10.1038/s41467-023-44615-y
摘要
Abstract Structure deterioration and side reaction, which originated from the solvated H 2 O, are the main constraints for the practical deployment of both cathode and anode in aqueous Zn-ion batteries. Here we formulate a weakly solvating electrolyte to reduce the solvating power of H 2 O and strengthen the coordination competitiveness of SO 4 2− to Zn 2+ over H 2 O. Experiment results and theoretical simulations demonstrate that the water-poor solvation structure of Zn 2+ is achieved, which can (i) substantially eliminate solvated-H 2 O-mediated undesirable side reactions on the Zn anode. (ii) boost the desolvation kinetics of Zn 2+ and suppress Zn dendrite growth as well as structure aberration of the cathode. Remarkably, the synergy of these two factors enables long-life full cells including Zn/NaV 3 O 8 ·1.5H 2 O, Zn/MnO 2 and Zn/CoFe(CN) 6 cells. More importantly, practical rechargeable AA-type Zn/NVO cells are assembled, which present a capacity of 101.7 mAh and stability of 96.1% capacity retention after 30 cycles at 0.66 C.
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