Two polymer-derived SiOC ceramics with different amount of carbon were synthesized either as dense or porous SiOC powders. The dense materials were produced up to a maximum temperature of 1400 ◦C and show a phase separated nanostructure consisting of SiO2-rich clusters, nanocrystalline SiC and nanocrystalline carbon phase. The corresponding porous materials were obtained by etching the silica phase of the dense SiOC with 20% HF solution. The electrochemical properties of the dense and porous SiOC ceramics in terms of lithium insertion/extraction were studied. Accordingly, the SiOC materials show a first lithium insertion capacity between 380 and 648 mAh g−1 followed by significantly lower extraction capacities between 102 and 272 mAh g−1. We consider the free carbon phase present in the ceramic as the major lithium intercalating agent. The porous samples show a stable electrochemical behavior up to 30 cycles while for the dense materials the efficiency drops to almost zero after 10 cycles.

Lithium Insertion into Dense and Porous Carbon-Rich Polymer-Derived SiOC Ceramics

Sorarù, Gian Domenico
2012-01-01

Abstract

Two polymer-derived SiOC ceramics with different amount of carbon were synthesized either as dense or porous SiOC powders. The dense materials were produced up to a maximum temperature of 1400 ◦C and show a phase separated nanostructure consisting of SiO2-rich clusters, nanocrystalline SiC and nanocrystalline carbon phase. The corresponding porous materials were obtained by etching the silica phase of the dense SiOC with 20% HF solution. The electrochemical properties of the dense and porous SiOC ceramics in terms of lithium insertion/extraction were studied. Accordingly, the SiOC materials show a first lithium insertion capacity between 380 and 648 mAh g−1 followed by significantly lower extraction capacities between 102 and 272 mAh g−1. We consider the free carbon phase present in the ceramic as the major lithium intercalating agent. The porous samples show a stable electrochemical behavior up to 30 cycles while for the dense materials the efficiency drops to almost zero after 10 cycles.
2012
P., Dibandjo; M., Graczyk Zajac; R., Riedel; V. S., Pradeep; Sorarù, Gian Domenico
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11572/91786
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