Co-insertion of K+ and Ca2+ in vanadium oxide as high-performance aqueous zinc-ion battery cathode material

被引:12
作者
Li, Zhaoao [1 ,2 ]
Yang, Linyu [1 ,2 ]
Wang, Shuying [1 ,2 ]
Zhu, Kunjie [3 ]
Li, Haibing [4 ]
机构
[1] Xinjiang Univ, Xinjiang Key Lab Solid State Phys & Devices, Urumqi 830046, Peoples R China
[2] Xin Jiang Univ, Sch Phys & technol, Urumqi 830046, Xinjiang, Peoples R China
[3] Univ Shanghai Sci & Technol, China Inst Energy Mat Sci, Shanghai 200093, Peoples R China
[4] China Jiliang Univ, Coll Modern Sci & Technol, Jinhua 322000, Peoples R China
基金
中国国家自然科学基金;
关键词
K0.02Ca0.18V2O5 center dot 0.7H(2)O; Zinc ion battery; Co-inserting; HIGH-ENERGY; INTERCALATION; V2O5;
D O I
10.1016/j.jallcom.2024.174589
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
Inserting metal ions into vanadium oxides can effectively improve their electrochemical properties, and the insertion of different single metal ions into vanadium-based compounds can enhance their electrochemical performance in different ways. Moreover, the insertion of multiple metal ions into vanadium-based compounds may provide a synergistic effect. Therefore, in this work a K0.02Ca0.18V2O5 center dot 0.7H(2)O (KCaVOH) cathode material was obtained by co-inserting the monovalent metal ion K+ and the divalent metal ion Ca2+ into vanadium oxide through a one-step hydrothermal method. The insertion of K+ enhances the structural stability of the cathode material, while the insertion of Ca2+ increases the layer spacing between the V-O layers and improves the specific capacity of the cathode material. The co-insertion of K+ and Ca2+ effectively enhances the electrochemical performance of V2O5 center dot 1.6H(2)O, and the KCaVOH cathode provides a high specific capacity of 410 mAh center dot g(-1) at 0.3 A center dot g(-1). Moreover, the capacity still reaches 265 mAh center dot g(-1) after 1800 cycles at 5 A center dot g(-1). This method provides a strategy for significantly enhancing the electrochemical performance of vanadium-based cathode materials.
引用
收藏
页数:9
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