Influence of high-temperature oxidation on photoluminescent properties of white Si-O-C(-H) ceramics

被引:9
作者
Narisawa, Masaki [1 ]
Watase, Seiji [2 ]
Matsukawa, Kimihiro [2 ]
Kawai, Taketoshi [3 ]
Kawamoto, Yasushi [1 ]
Matsui, Toshiyuki [1 ]
Iwase, Akihiro [1 ]
机构
[1] Osaka Prefecture Univ, Grad Sch Engn, Naka Ku, Sakai, Osaka 5998531, Japan
[2] Osaka Municipal Tech Res Inst, Joto Ku, Osaka 5368553, Japan
[3] Osaka Prefecture Univ, Grad Sch Sci, Naka Ku, Sakai, Osaka 5998531, Japan
关键词
Silicon oxycarbide; Precursor method; Oxidation resistance; Photoluminescence; Decarbonization; THIN-FILMS; GEL; LUMINESCENCE; PRECURSOR;
D O I
10.1016/j.jnoncrysol.2014.03.005
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
Si-O-C(-H) ceramics were prepared by pyrolyzing densely cross-linked polysiloxane particles in hydrogen at temperatures of 800, 900 and 1100 degrees C. Thermogravimetric-differential thermal analysis (TG-DTA) curves of these Si-O-C(-H) ceramics in an air flow revealed that the oxidation resistance strongly depended on the decarbonization temperature. On the other hand, these decarbonized samples were oxidized in dry air flow at temperatures of 300, 500, 700, 1000 and 1200 degrees C. After the oxidation in air, photoluminescent (PL) spectra and Fourier transform infrared (FTIR) spectra of the oxidized samples were investigated. In partly organic Si-O-C(-H) ceramics with high H/C ratios, the intensity of blue PL simultaneously decreased with rapid oxidation. Residual weak PL peaks are probably assigned to defects in silica formed on particle surfaces. In dense Si-O-C(-H) ceramics with a relatively low H/C ratio, the intensity of white PL gradually decreased with moderate oxidation and the PL peak position shifted to longer wavelengths. Intensity of phosphorescence of the dense Si-O-C(-H) ceramics was also weakened after oxidation. The decrease of phosphorescence intensity, however, began at a rather low temperature range as compared with that of the apparent PL. (C) 2014 Elsevier B.V. All rights reserved.
引用
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页码:1 / 5
页数:5
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