Lithium Titanate Tailored by Cathodically Induced Graphene for an Ultrafast Lithium Ion Battery
Nonoxidative cathodically induced graphene (CIG) here incorporates conductive agents for Li4Ti5O12 (LTO) anode materials. The tailored LTO/CIG composite is fabricated by controlled hydrolysis of tetrabutyl titanate in the presence of nonoxidative defect‐free cathodically induced graphene (CIG) and o...
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Veröffentlicht in: | Advanced functional materials 2014-07, Vol.24 (27), p.4349-4356 |
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Sprache: | eng |
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Zusammenfassung: | Nonoxidative cathodically induced graphene (CIG) here incorporates conductive agents for Li4Ti5O12 (LTO) anode materials. The tailored LTO/CIG composite is fabricated by controlled hydrolysis of tetrabutyl titanate in the presence of nonoxidative defect‐free cathodically induced graphene (CIG) and oxalic acid in a mixed solvent of ethanol and water, followed by hydrothermal reaction and a calcination treatment. Due to the introduction of defect‐free graphene, the resulting LTO/CIG composite shows an excellent electrical conductivity (1.2 × 10−4 S cm−1) and Li+ diffusion coefficient (1.61 × 10−12 cm2 s−1). As a result, the tuned LTO/CIG composite exhibits outstanding electrochemical performance, including excellent cycling stability (the capacity retention ratios after 500 cycles at 0.5 C is 96.2%) and a remarkable rate capability (162 mAh g−1 at 10C, 126 mAh g−1 at 100 C). A specific energy of 272 Wh kg−1 at power of 136 W kg−1 is observed when cycling against Li‐foil. Even during 36 s of charge/discharge, the specific energy of LTO/CIG composite remains at 166 Wh kg−1.
Defect‐free cathodically induced graphene (CIG) is exploited to tailor the electrical conductivity and Li+ diffusion coefficient of Li4Ti5O12 (LTO) anode materials for lithium ion batteries. The as‐tuned LTO/CIG exhibits excellent cycling stability (capacity retention ratio after 500 cycles at 0.5 C is 96.2%) and a remarkable rate capability (162 mAh g−1 at 10 C, 126 mAh g−1 at 100C). |
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ISSN: | 1616-301X 1616-3028 |
DOI: | 10.1002/adfm.201304263 |