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Published on: February 7, 2017
Structural evolutions in polymer-derived carbon-rich amorphous silicon carbide
Kewei Wang1, Baisheng Ma, Xuqin Li
1Science and Technology on Thermostuctural Composite Materials Laboratory, Northwestern Polytechnical University , Xi'an, Shaanxi 710072, People's Republic of China.
This study details structural changes in amorphous silicon carbide (SiC) derived from polycarbosilane. Increasing temperatures refine the SiC matrix and transform free carbon into nanocrystalline graphite.
Area of Science:
- Materials Science
- Ceramics Engineering
- Nanotechnology
Background:
- Polycarbosilane-derived amorphous silicon carbide (SiC) is a promising material with tunable properties.
- Understanding its structural evolution during pyrolysis is crucial for optimizing its performance.
Purpose of the Study:
- To investigate the semiquantitative structural evolutions in carbon-rich amorphous SiC derived from polycarbosilane.
- To elucidate the transformation mechanisms of the Si-containing matrix and free-carbon phases with increasing pyrolysis temperature.
Main Methods:
- Combined experimental and analytical techniques for semiquantitative investigation.
- Analysis of structural changes in the Si-containing matrix and free-carbon phases.
- Characterization of defects and phase transitions during pyrolysis.
Main Results:
- The material consists of a Si-containing matrix (SiC4, SiCxOx-4, Si-C-C-Si/Si-C-H defects) and a free-carbon phase.
- Increasing pyrolysis temperature orders the matrix (SiC2O2 to SiCO3) and initiates β-SiC crystallization above 1250 °C.
- Free carbon transitions from amorphous to nanocrystalline graphite, with cluster size initially decreasing then increasing, and C-dangling bonds continuously decreasing.
Conclusions:
- The structural evolution involves matrix ordering, crystallization, and transformation of free carbon.
- Carbon cluster growth is explained by Ostwald ripening and a 2D grain growth model.
- The decrease in C-dangling bonds is directly linked to the lateral growth of carbon clusters.
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