Ethanediamine Intercalation Induced Hydrogen Bond Network in Vanadium Oxide for Ultralong-Life Aqueous Ammonium Ion Batteries

被引:0
|
作者
Lu, Tzu-Hao [1 ,2 ]
Liu, Qiyu [2 ]
He, Jinjun [2 ]
Liu, Hao [2 ]
Yu, Yanxia [2 ]
Wang, Yi [1 ]
Lu, Xihong [2 ]
机构
[1] Guiyang Univ, Coll Chem & Mat Engn, Guiyang 550005, Guizhou, Peoples R China
[2] Sun Yat Sen Univ, Sch Chem, Sch Chem Engn & Technol, Key Lab Low Carbon Chem & Energy Conservat Guangdo, Guangzhou 510275, Peoples R China
基金
中国国家自然科学基金;
关键词
Aqueous ammonium ion batteries; Organic-inorganic hybrid materials; Ethanediamine; Hydrogen bonding; High stability; NH4+;
D O I
10.1002/batt.202400426
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Aqueous ammonium-ion batteries (AAIBs) have received tremendous attention as a potential energy technology, but their development is severely challenged by the fact that the as-reported electrode materials are usually unable to meet the requirements of high capacity and high stability simultaneously. Herein, an organic-inorganic hybrid material of ethanediamine (EDA) intercalated vanadium oxide (VO-EDA) is synthesized as a high-performance anode material for AAIBs. The intercalated EDA molecules not only act as an electron donor to bind with NH4+, but also form hydrogen bonding network structures with vanadium oxides to facilitate charge/ion transfer. As a result, this hybrid material provides a high specific capacity of 104.4 mAh g(-1) at 0.5 A g(-1) and good cycling stability after 5000 cycles 10 A g(-1) with a coulombic efficiency of ~100 %. Moreover, the ammonium-ion full cell based on VO-EDA anode and NiHCF cathode achieves a specific capacity of 55 mAh g(-1) at 0.1 A g(-1) and impressive cycling stability with 88.6 % capacity retention after 10000 cycles at 5 A g(-1).
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页数:8
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