Glass-Ceramics Containing Nano-Crystallites of Oxide Semiconductor
Glass-Ceramics Containing Nano-Crystallites of Oxide Semiconductor
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DOI:
10.5772/intechopen.83927
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发表时间:
2010-09
期刊:
影响因子:
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通讯作者:
H. Masai;Y. Takahashi;T. Fujiwara
中科院分区:
文献类型:
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作者:
H. Masai;Y. Takahashi;T. Fujiwara
1.1 Glass and Crystal Inorganic glass materials generally possess high transparency, good formability, and tuneable chemical composition range. Since glass has no grain boundary, which is a characteristic of liquid, attained high transparency of glass makes it to be a fundamental material for our daily life, for examples, window, display panel glass and optical glass fibres. The good formability is originated from the random network structure with interstitial free volume, and therefore, large and long glassy material can be prepared much easier than inorganic crystal. Note that the term “random” in glass means a lack of the longrange ordering. Actually in glass there is a short-range ordering of atoms that constitute various coordination polyhedra. Thus, the short-range ordering in amorphous is basically identical to that in crystal. On the other hand, the random network of glass closely correlates with the chemical composition diversity, which in turn allows us to tailor physical property and various functionalities. The diversity is also a unique characteristic of amorphous glass materials. The most conventional definition of glass is ′′an amorphous material possessing the glass transition behaviour”. Figure 1 shows a typical volume change of glass and crystal as a function of temperature. In the case of crystal, transition from liquid to solidified crystal occurs at the melting temperature, Tm. On the other hand, a glass material takes the supercooled state below the Tm, and shows the transition to glass in the temperature range where the viscosity of glass increases to 1013 dPa·s. Temperature at which transition from supercooled liquid to glass occurs is mentioned as the glass transition temperature, Tg. In the temperature region, some physical parameters of glass material show “some steep” change. Since the Tg is a fictive temperature that depends on the fabrication process, a glass can take several values of Tg depending on the cooling rate. As shown in Fig. 1, there is a volume difference between crystal and the glass, which originates from the free volume of glass material possessing the random network. Because of the random network structure, the Gibbs free energy of a glass material is inherently larger than that of the corresponding crystal, and glass materials exist as a metastable state. It means that phase transition of glass to crystalline phase can progress above the Tg, at which migration of the compositional units 2