Activated natural porous silicate for a highly promising SiOx nanostructure finely impregnated with carbon nanofibers as a high performance anode material for lithium-ion batteries

被引:25
作者
Back, Chang-Keun [1 ]
Kim, Tai-Jin [2 ]
Choi, Nam-Soon [3 ]
机构
[1] Hanwha Chem Co Ltd, Cent R&D Ctr, Daejeoun City 305350, South Korea
[2] Univ Suwon, Dept Chem Engn, Kyunggido 445743, South Korea
[3] UNIST, Sch Energy & Chem Engn, Ulsan 689798, South Korea
关键词
HIGH-CAPACITY; ELECTROCHEMICAL PROPERTIES; ENERGY-CONVERSION; LI; NANOWIRES; OXYGEN; COMPOSITES; INSERTION; ELECTRODE;
D O I
10.1039/c4ta02706j
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
A highly promising anode material with an amorphous SiOx nanostructure finely impregnated with carbon nanofibers is presented. The nanostructure material has a unique integral feature in that carbon nanofibers smaller than several nm in diameter are finely dispersed in amorphous SiOx media in an aligned manner. The synthetic route to fabricate the nanostructure is very simple and easy, using natural porous silicate, sepiolite, activated through the process of sintering and acid treatments on carbon source-loaded sepiolite nanocomposites. Upon the treatments, the nanocomposite material is changed in respect of its structure and chemical composition from crystalline Mg silicate to the carbon nanofiber-impregnated amorphous SiOx phase (CNF-SiOx nanostructure), and the electrochemical activity is greatly improved. The CNF-SiOx nanostructure exhibits excellent electrochemical performance with a reasonably high capacity of approximately 720 mA h g(-1) for a current density of 70 mA g(-1) (C/10 rate) and outstanding rate capability with a capacity retention of 96.8% for a current density of 700 mA g(-1) and 87% at 1400 mA g(-1) relative to that at 35 mA g(-1), even at a high electrode loading level above 8 mg cm(-2). The cycling performance is also very stable, with a capacity retention of 94.7% over 50 cycles at a rate of 350 mA g(-1) and with a Coulombic efficiency above 99%.
引用
收藏
页码:13648 / 13654
页数:7
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