Crystal modification of iron oxide scale by potassium addition and its application to lithium-ion battery anodes

被引:12
作者
Jung, Dong-Won [1 ]
Han, Sang-Wook [1 ]
Kong, Byung-Seon [2 ]
Oh, Eun-Suok [1 ]
机构
[1] Univ Ulsan, Sch Chem Engn, Ulsan 680749, South Korea
[2] KCC Cent Res Inst, Yongin 446912, Kyunggi Do, South Korea
关键词
Iron oxide scale; Potassium iron oxide; Anode active materials; Lithium-ion battery; Electrochemical characterization; ALPHA-FE2O3; LI; INTERCALATION; NANOPARTICLES; WUSTITE; STORAGE; SIZE;
D O I
10.1016/j.jpowsour.2013.05.091
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
This paper proposes a valuable method to reuse the iron oxide scale (105) often produced in the steel industry as an anode active material in lithium-ion batteries (LIBs). The IOS samples are prepared via quenching of carbon steel and simple oxidation at a high temperature with or without sequential treatment by potassium hydroxide. Morphological and physical characterizations confirm the formation of a lamellar structure of orthorhombic KFeO2 with a high degree of crystallinity in the potassium-added IOSs. Additionally, the potassium addition decreases the particle size of the crystals and increases the d-spacing between crystal layers. Electrochemical performance tests show that the discharge capacities of the IOS samples monotonically increased with increasing number of charge/discharge cycles regardless of the existence of potassium. In addition, the rate of increase is larger in the potassium-added LOS samples containing the lamellar KFeO2 structure. Consequently, after prolonged cycling (more than 500 cycles), the potassium-added IOS sample retains a discharge capacity of 1020 mAh g(-1) with good cycling stability, while the LOS quenched sample only exhibits a capacity of 956 mAh g(-1). This result is attributed to the unique structure of the KFeO2 crystals formed in the potassium-added IOS particles. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:357 / 364
页数:8
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