Thermal Stability, Phase Evolution, and Crystallization in Si‐B‐C‐N Ceramics Derived from a Polyborosilazane Precursor

Abstract

Amorphous Si‐B‐C‐N ceramic powder samples obtained by thermolysis of boron‐modified polysilazane, {B[C 2 H 4 Si(H)NH] 3 } n , were isothermally annealed at different temperatures (1400–1800°C) and hold times (3, 10, 30, and 100 h). A qualitative and semiquantitative analysis of the crystallization behavior of the materials was performed using X‐ray diffraction (XRD). The phase evolution was additionally followed by 11 B and 29 Si MAS NMR as well as by FT‐IR spectroscopy in transmission and diffuse reflection (DRIFTS) modes. Bulk chemical analyses of selected samples were performed to determine changes in the chemistry/phase composition of the materials. It was observed that silicon carbide is the first phase to nucleate around 1400–1500°C, whereas silicon nitride nucleates at and above 1700°C. Crystallization accelerates with increasing annealing temperature and proceeds with increasing annealing time. Furthermore, the surface area of the powders strongly influences the thermal stability of silicon nitride and thus controls overall chemical and phase composition of the materials on thermal treatment.