The structure evolution of hollow SiOC ceramic microspheres prepared with solvothermal method

Hollow silicon oxycarbide (SiOC) ceramic microspheres were synthesized through solvothermal process of vinyltriethoxysilane in NaOH solution with subsequent pyrolysis at high temperature. Increasing the synthesis temperature not only reduces the Si-C bond and C content in SiOC ceramics, but also transforms the amorphous SiOC ceramics into cristobalite SiO2 after carbonization. The rearrangement reaction of oxygen-enriched structural units results in the increase of SiO2C2 unit. No phase separation occurs at 1400 degrees C, and SiC nano-crystals are mainly come from the carbothermal reduction reaction of SiO2 with free C. The size change of SiO2 nanograins were further investigated by HF etching. The porous carbon is obtained after removal of SiO2, while HF etching has no effect on the structure of free C. The C content affects the structure evolution of SiOC ceramics significantly. Although the size of SiO2 grows as increase of pyrolysis temperature, the high C content inhibits the crystallization and growth of SiO2 during the pyrolysis process.

Automated summary

Hollow silicon oxycarbide (SiOC) ceramic microspheres were synthesized by solvothermal process and subsequent high-temperature pyrolysis. Increasing the synthesis temperature leads to a decrease in Si-C bond and C content in SiOC ceramics, and transforms amorphous SiOC ceramics into cristobalite SiO2. The rearrangement reaction of oxygen-enriched structural units increases the SiO2C2 unit. SiC nano-crystals mainly come from the carbothermal reduction reaction of SiO2 with free C at 1400 degrees C without phase separation. The size change of SiO2 nanograins was investigated by HF etching, resulting in the obtaining of porous carbon after removal of SiO2.