This study presents new experimental data on the thermodynamic stability of SiC(O) and SCN(O) ceramics derived from the pyrolysis of polymeric precursors: SMP‐10 (polycarbosilane), PSZ‐20 (polysilazane), and Durazane‐1800 (polysilazane) at 1200°C. There are close similarities in the structure of the polysilazanes, but they differ in crosslinking temperature. High‐resolution X‐ray photoelectron spectroscopy shows notable differences in the microstructure of all polymer‐derived ceramics (PDCs). The enthalpies of formation (∆
- Award ID(s):
- 1743701
- NSF-PAR ID:
- 10213917
- Date Published:
- Journal Name:
- Materials
- Volume:
- 14
- Issue:
- 3
- ISSN:
- 1996-1944
- Page Range / eLocation ID:
- 614
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Abstract H °f, elem) of SiC(O) (from SMP‐10), SCN(O) (from PSZ‐20), and SCN(O) (from Durazane‐1800) are −20 ± 4.63, −78.55 ± 2.32, and −85.09 ± 2.18 kJ/mol, respectively. The PDC derived from Durazane‐1800 displays greatest thermodynamic stability. The results point to increased thermodynamic stabilization with addition of nitrogen to the microstructure of PDCs. Thermodynamic analysis suggests increased thermodynamic drive for forming SiCN(O) microstructures with an increase in the relative amount of SiNx C4−x mixed bonds and a decrease in silica. Overall, enthalpies of formation suggest superior stabilizing effect of SiNx C4−x compared to SiOx C4−x mixed bonds. The results indicate systematic stabilization of SiCN(O) structures with decrease in silicon and oxygen content. The destabilization of PDCs resulting from higher silicon content may reach a plateau at higher concentrations. -
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