Effect of sintering temperature on the developed crystalline phases, optical and electrical properties of 5ZnO-2TiO2-3P2O5 glass

被引:6
|
作者
Morsi, Morsi M. [1 ]
Margha, Fatma H. [1 ]
Morsi, Reham M. M. [2 ]
机构
[1] Natl Res Ctr, Glass Res Dept, 33 El Bohoth St,PO 12622, Giza, Egypt
[2] Natl Res Ctr, Dept Phys Chem, 33 El Bohoth St,PO 12622, Giza, Egypt
关键词
Zinc phosphate; Titanophosphate; Glass ceramics; XRD; Electrical properties; SILICATE-GLASSES; PHOSPHATE; TITANOPHOSPHATE; CONDUCTIVITY; ABSORPTION;
D O I
10.1016/j.jallcom.2018.08.045
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Glass of the composition 5ZnO-2TiO(2)-3P(2)O(5) was prepared by the melt-quenching technique. The prepared samples were heat-treated at the nucleation (625 degrees C) and crystallization (875 degrees C) temperatures for different soaking times. SEM, XRD, UV-Vis, DSC and electrical measurements were used. Ti(PO4) and Zn-3(PO4)(2) phases were formed at the nucleation temperature; while, Ti5O4(PO4)(4) and alpha-Zn2P2O7 phases were observed at the crystallization temperature. Long soaking time caused color fading or formation of opaque white samples due to the decrease of Ti3+ ions or increase of Ti4+ ions, respectively. The formation of Ti3+ ions causes a development of violet color with absorption bands in the range 400-800 nm. SEM suggested that prolonged heating at the crystallization temperature caused disintegration of the formed phases. The electrical conductivities of the studied samples at the low and high measuring temperatures occur via electrons revealing their suitability to be applied as semiconductors. The values of sac and dielectric constant epsilon' increase with rising the sintering temperature. The epsilon' of the as-prepared sample (19.23) is increased to 152.45 or 189.11 when heat-treated at the nucleation temperature for 4 h and at crystallization temperature for 15 min, respectively. Samples of high epsilon' values represent promising candidates for energy storage in electronic devices. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:758 / 765
页数:8
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