Graphite microspheres decorated with Si particles derived from waste solid of organosilane industry as high capacity anodes for Li-ion batteries

We report the decoration of commercial graphite microspheres (GMs) with Si particles as anode materials for Li-ion batteries. The Si particles are obtained from solid Si waste of organosilane industry that is acid-washed to remove the impurities and further ground. The GMs with a size of 5–40 μm as...

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Published inJournal of power sources Vol. 228; pp. 112 - 119
Main Authors Yu, Jing, Zhan, Hanhui, Wang, Yanhong, Zhang, Zailiei, Chen, Han, Li, Hong, Zhong, Ziyi, Su, Fabing
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier B.V 15.04.2013
Elsevier
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Summary:We report the decoration of commercial graphite microspheres (GMs) with Si particles as anode materials for Li-ion batteries. The Si particles are obtained from solid Si waste of organosilane industry that is acid-washed to remove the impurities and further ground. The GMs with a size of 5–40 μm as main active material, Si particles with a size of 1–10 μm as an additive, and sucrose dissolved in water as a binder are mixed and followed by carbonization to obtain Si/C composites containing graphite, Si, and amorphous carbon generated from sucrose. It is found that the composite containing 60.5 wt% of GMs, 22.1 wt% of Si, and 17.4 wt% of amorphous carbon obtained at 800 °C for 5 h shows the best electrochemical performance with a specific capacity of 522.6 mA h g−1 at the current density of 50 mA g−1 and 306.9 mA h g−1 at 500 mA g−1, much higher than those of GMs. Its capacity retention at 500 mA g−1 attains 93.9% after 20 cycles. The work demonstrates the possibility for utilization of the industrial Si waste to enhance graphite anode materials in Li-ion batteries. ► Si waste from organosilane industry was used for preparation of Si/C composite. ► Graphite microspheres were decorated with Si particles and sucrose as the binder. ► The Si/C composite anodes show the enhanced electrochemical performance.
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ISSN:0378-7753
1873-2755
DOI:10.1016/j.jpowsour.2012.11.083