Characterization of free carbon in the as-thermolyzed Si-B-C-N ceramic from a polyorganoborosilazane precursor
作者机构:Materials Processing SectionDepartment of Metallurgical and Materials EngineeringIndian Institute of Technology MadrasChennai 600036Tamil NaduIndia Analytical Spectroscopy and Ceramics GroupPCM EntityVikram Sarabhai Space CentreThiruvananthapuram 695022India
出 版 物:《Journal of Advanced Ceramics》 (先进陶瓷(英文))
年 卷 期:2013年第2卷第4期
页 面:325-332页
核心收录:
学科分类:0808[工学-电气工程] 0809[工学-电子科学与技术(可授工学、理学学位)] 0817[工学-化学工程与技术] 08[工学] 0805[工学-材料科学与工程(可授工学、理学学位)] 080502[工学-材料学] 0702[理学-物理学]
基 金:We gratefully acknowledge the financial support from the Vikram Sarabhai Space Centre Thiruvananthapuram through ISRO-IITM cell(Project No.ICSR/ISRO-IITM/MET/08-09/122/RAVK)
主 题:synthesis polyorganoborosilazane precursor-derived ceramic Si-B-C-N Raman spectroscopy free carbon
摘 要:Polyorganoborosilazane((B[C_(2)H_(4)-Si(CH_(3))NH]_(3))n)was synthesized via monomer route from a single-source precursor and thermolyzed at 1300℃in argon *** as-thermolyzed Si-B-C-N ceramic was characterized using X-ray diffraction(XRD)and Raman *** crystallization behavior of silicon carbide in the as-thermolyzed amorphous Si-B-C-N matrix was understood by XRD studies,and the crystallite size calculated using Scherrer equation was found to increase from 2 nm to 8 nm with increase in dwelling ***,Raman spectroscopy was used to characterize the free carbon present in the as-thermolyzed *** peak positions,intensities and full width at half maximum(FWHM)of D and G bands in the Raman spectra were used to study and understand the structural disorder of the free *** G peak shift towards 1600 cm-1 indicated the decrease in cluster size of the free *** cluster diameter of the free carbon calculated using TK(Tuinstra and Koenl)equation was found to decrease from 6.2 nm to 5.4 nm with increase in dwelling time,indicating increase in structural disorder.