Effect of Precursor on Speciation and Nanostructure of SiBCN Polymer-Derived Ceramics

被引:62
作者
Widgeon, Scarlett [1 ]
Mera, Gabriela [2 ]
Gao, Yan [2 ]
Sen, Sabyasachi [1 ]
Navrotsky, Alexandra [1 ,3 ,4 ]
Riedel, Ralf [2 ]
机构
[1] Univ Calif Davis, Dept Chem Engn & Mat Sci, Davis, CA 95616 USA
[2] Tech Univ Darmstadt, Inst Mat Wissensch, D-64287 Darmstadt, Germany
[3] Univ Calif Davis, Peter A Rock Thermochem Lab, Davis, CA 95616 USA
[4] Univ Calif Davis, NEAT ORU, Davis, CA 95616 USA
基金
美国国家科学基金会;
关键词
SOLID-STATE NMR; C-N CERAMICS; AMORPHOUS-SILICON OXYCARBIDE; CARBON; VISCOSITY; BEHAVIOR; NITRIDE; GLASSES; PHASE;
D O I
10.1111/jace.12192
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
A comparative structural study of silicon borocarbonitride polymer-derived ceramics synthesized using polyborosilylcarbodiimide and polyborosilazane precursors is carried out using high-resolution, multinuclear, one- and two- dimensional NMR spectroscopy. The polyborosilylcarbodiimide-derived ceramics contain relatively pure Si3N4 and C nanodomains with the BN domains being present predominantly at the interface such that the bonding at the interface consists of SiNB, SiNC, and BNC linkages. In contrast, the structure of the polyborosilazane-derived ceramics consists of significant amount of mixed bonding in the nearest-neighbor coordination environments of Si and B atoms leading to the formation of SiCxN4x (0x4) tetrahedral units and BCN2 triangular units. The interfacial region between the SiCN and C nanodomains is occupied by the BCN phase. These results demonstrate that the chemistry of the polymeric precursors exerts major influence on the microstructure and bonding in their derived ceramics even when the final chemical compositions of the latter are similar.
引用
收藏
页码:1651 / 1659
页数:9
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