Multi-metal ions co-regulated vanadium oxide cathode toward long-life aqueous zinc-ion batteries

被引:9
作者
Ma, Ming-Yang
Liu, Yan
Yang, Jia-Lin
Li, Shu-Ying
Du, Miao
Liu, Dai-Huo
Hao, Ze-Lin
Guo, Jin-Zhi [1 ]
Wu, Xing-Long [1 ,2 ]
机构
[1] Northeast Normal Univ, MOE, Key Lab UV Light Emitting Mat & Technol, Changchun, Jilin, Peoples R China
[2] Northeast Normal Univ, Dept Chem, Changchun 130024, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
Aqueous zinc-ion batteries; Vanadium oxide; Multi-ion engineering strategy; Interlayer spacing; Synergistic effect; PENTOXIDE; INTERCALATION; RADII;
D O I
10.1016/j.jcis.2024.05.065
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Interlayer intercalation engineering shows great feasibility to improve the structure stability of the layered oxides. Although high Zn-storage capability has been attained based on the pillar effect of multifarious intercalants, an in-depth understanding the synergistic effect of intercalated multiple metal ions is still in deficiency. Herein, alkali metal ion K+, alkaline earth metal ion Mg2+ and trivalent metal ion Al3+ are introduced into the VO interlayer of V2O5. Due to the different electronegativity and hydrated ion radius of K+, Mg2+ and Al3+, adjusting the relative proportions of these metal ions can achieve an appropriate interlayer spacing, stable layer structure and regular morphology, which facilitates the transport kinetics of Zn2+. Under the synergistic effect of preintercalated multi-metal ion, the optimal tri-metal ion intercalated hydrated V2O5 cathode exhibits a high specific capacity of 382.4 mAh g-1 at 0.5 A g-1, and long-term cycling stability with capacity retention of 86 % after 2000 cycles at the high current density of 10 A g-1. Ex-situ and kinetic characterizations reveal the fast charge transfer and reversible Zn2+ intercalation mechanism. The multi-ion engineering strategy provides an effective way to design desirable layered cathode materials for aqueous zinc-ion batteries.
引用
收藏
页码:174 / 181
页数:8
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