Affiliation:
1. School of Materials Science and Engineering Hunan Provincial Key Laboratory of Electronic Packaging and Advanced Functional Materials Central South University Changsha Hunan 410083 P. R. China
2. Department of Materials Science and Engineering City University of Hong Kong 83 Tat Chee Avenue, Kowloon Hong Kong 999077 P. R. China
3. School of Physics and Electronics Hunan University Changsha Hunan 410082 P. R. China
Abstract
AbstractAqueous rechargeable zinc‐ion batteries (ARZBs) are impeded by the mutual problems of unstable cathode, electrolyte parasitic reactions, and dendritic growth of zinc (Zn) anode. Herein, a triple‐functional strategy by introducing the tetramethylene sulfone (TMS) to form a hydrated eutectic electrolyte is reported to ameliorate these issues. The activity of H2O is inhibited by reconstructing hydrogen bonds due to the strong interaction between TMS and H2O. Meanwhile, the preferentially adsorbed TMS on the Zn surface increases the thickness of double electric layer (EDL) structure, which provides a shielding buffer layer to suppress dendrite growth. Interestingly, TMS modulates the primary solvation shell of Zn2+ ultimately to achieve a novel solvent co‐intercalation ((Zn‐TMS)2+) mechanism, and the intercalated TMS works as a “pillar” that provides more zincophilic sites and stabilizes the structure of cathode (NH4V4O10, (NVO)). Consequently, the Zn||NVO battery exhibits a remarkably high specific capacity of 515.6 mAh g−1 at a low current density of 0.2 A g−1 for over 40 days. This multi‐functional electrolytes and solvent co‐intercalation mechanism will significantly propel the practical development of aqueous batteries.
Funder
National Natural Science Foundation of China
Subject
General Chemistry,Catalysis
Cited by
68 articles.
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