Preparation and Characterization of Porous Silicon and Carbon Composite as an Anode Material for Lithium Rechargeable Batteries
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The composite of porous silicon (Si) and amorphous carbon (C) is prepared by pyrolysis of a nano-porousSi + pitch mixture. The nano-porous Si is prepared by mechanical milling of magnesium powder with silicon monoxide(SiO) followed by removal of MgO with hydrochloric acid (etching process). The Brunauer-Emmett-Teller (BET) surfacearea of porous Si (64.52 m2g−1) is much higher than that before etching Si/MgO (4.28 m2g−1) which indicates poresare formed in Si after the etching process. Cycling stability is examined for the nano-porous Si + C composite and theresult is compared with the composite of nonporous Si + C. The capacity retention of the former composite is 59.6%after 50 charge/discharge cycles while the latter shows only 28.0%. The pores of Si formed after the etching process isbelieved to accommodate large volumetric change of Si during charging and discharging process.
Abstract
The composite of porous silicon (Si) and amorphous carbon (C) is prepared by pyrolysis of a nano-porousSi + pitch mixture. The nano-porous Si is prepared by mechanical milling of magnesium powder with silicon monoxide(SiO) followed by removal of MgO with hydrochloric acid (etching process). The Brunauer-Emmett-Teller (BET) surfacearea of porous Si (64.52 m2g−1) is much higher than that before etching Si/MgO (4.28 m2g−1) which indicates poresare formed in Si after the etching process. Cycling stability is examined for the nano-porous Si + C composite and theresult is compared with the composite of nonporous Si + C. The capacity retention of the former composite is 59.6%after 50 charge/discharge cycles while the latter shows only 28.0%. The pores of Si formed after the etching process isbelieved to accommodate large volumetric change of Si during charging and discharging process.
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