Synchronous organic-inorganic co-intercalated ammonium vanadate cathode for advanced aqueous zinc-ion batteries

被引:0
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作者
Wenpei Kang [1 ]
Bingchen Zhang [1 ]
Zhurui Wang [1 ]
Zhengchunyu Zhang [2 ]
Mang Niu [3 ]
Xuguang An [4 ]
Zhenkai Mou [1 ]
Xiaoyu Fan [1 ]
Xuqiang Hu [1 ]
Baojuan Xi [2 ]
Shenglin Xiong [2 ]
机构
[1] School of Materials Science and Engineering, China University of Petroleum (East China)
[2] School of Chemistry and Chemical Engineering, Shandong University
[3] State Key Laboratory of Bio-fibers and Eco-textiles, Institute of Biochemical Engineering College of Materials Science and Engineering, Qingdao University
[4] School of Mechanical Engineering, Chengdu University
基金
中国国家自然科学基金;
关键词
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暂无
中图分类号
TM912 [蓄电池];
学科分类号
摘要
Vanadium-based cathode materials are attractive for aqueous zinc-ion batteries (AZIBs) owing to the high capacity from their open frameworks and multiple valences.However,the cycle stability and rate capability are still restricted by the low electrical conductivity and trapped diffusion kinetics.Here,we propose an organic–inorganic co-intercalation strategy to regulate the structure of ammonium vanadate(NH4V4O10,NVO).The introduction of Al3+and polyaniline (PANI) induces the optimized layered structure and generation of urchin-like hierarchical construction (AP-NVO),based on heterogeneous nucleation and dissolution–recrystallization growth mechanism.Owing to these favorable features,the AP-NVO electrode delivers a desirable discharge capacity of 386 mA h g-1at 1.0 A g-1,high-rate capability of 263 m A h g-1at 5.0 A g-1and excellent cycling stability with 80.4%capacity retention over 2000cycles at 5.0 A g-1.Such satisfactory electrochemical performance is believed to result from the enhanced reaction kinetics provided by the stable layered structure and a high intercalation pseudo-capacitance reaction.These results could provide enlightening insights into the design of layered vanadium oxide cathode materials.
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页码:608 / 617
页数:10
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