Exploration of low-cost microporous Fe(III)-based organic framework as anode material for potassium-ion batteries

被引:59
作者
Deng, Qijiu [1 ]
Feng, Shuaishuai [1 ]
Hui, Peng [2 ]
Chen, Hetuo [3 ]
Tian, Congcong [1 ]
Yang, Rong [2 ]
Xu, Yunhua [1 ,4 ]
机构
[1] Xian Univ Technol, Sch Mat Sci & Engn, Int Res Ctr Composite & Intelligent Mfg Technol, Xian 710048, Peoples R China
[2] Xian Univ Technol, Sch Sci, Inst Chem Power Sources, Xian 710048, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Ceram, State Key Lab High Performance Ceram & Superfine, Shanghai 201899, Peoples R China
[4] Yulin Univ, Yulin 719000, Peoples R China
基金
中国博士后科学基金; 上海市自然科学基金;
关键词
Metal organic framework; Potassium-ion battery; Electrochemical performance; K-storage mechanism; INTERCALATION; ELECTRODES; CATHODE; SODIUM; SALTS; LI;
D O I
10.1016/j.jallcom.2020.154714
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
Potassium-ion (K-ion) batteries were regarded as the promising candidate for increasingly large-scale energy storage system, mainly due to the abundant resources, low standard potential as well as fast ion transport capability. Exploring suitable anode materials that can fully accommodate the large ionic radius of K+ have been a research hotspot. Herein, a low-cost iron based metal organic framework, namely MOF-235 was initially proposed as newly anode material for K-ion batteries. After in-situ composited with multiwall-carbon tubes (MCNTs), the as-prepared MOF-235/MCNTs composite can show a specific capacity of 132 mAh g(-1) over 200 cycles with remarkable rate property. The reaction mechanism was further investigated by XRD, FT-IR and XPS analysis. The superior K-storage behavior were ascribed to the large surface area of MOF-235, the enhanced electronic conductivity and the organic terephthalate moiety as the active site. These results are of significant to explore advanced anode materials for K-ion batteries. (c) 2020 Elsevier B.V. All rights reserved.
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页数:8
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