Temperature evolution of Raman spectrum of iron phosphate glass

被引:24
作者
Chakraborty, S. [1 ]
Arora, A. K. [2 ]
机构
[1] Indira Gandhi Ctr Atom Res, Surface & Nanosci Div, Kalpakkam 603102, Tamil Nadu, India
[2] Indira Gandhi Ctr Atom Res, Condensed Matter Phys Div, Kalpakkam 603102, Tamil Nadu, India
关键词
Raman spectroscopy; Iron phosphate glass; Structural relaxations; Glass transition; STRUCTURAL-PROPERTIES; X-RAY; SPECTROSCOPY; SCATTERING; WASTEFORMS; DYNAMICS; FEATURES; VALENCE; MELTS; TIME;
D O I
10.1016/j.vibspec.2012.02.012
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Iron phosphate glass that has glass transition T-g similar to 782 K, has been investigated between 81 and 873 K using Raman spectroscopy. After correcting for the thermal population factor, the reduced spectra are analyzed to obtain the mode wavenumbers and their line widths. A total of nine modes were followed as a function of temperature. The temperature dependences of mode wavenumbers of nearly all the modes are found to show anomalies near T-g. Below T-g, the asymmetric stretching of Q(1) tetrahedra of [P2O7](4-) units and Q(0) tetrahedra of [PO4](3-) units at 1090 and 946 cm(-1), respectively, exhibit conventional anharmonic behavior, whereas the network vibration, iron polyhedral and PO4 network bending modes at 170, 306 and 420 cm(-1), respectively, show hardening suggesting stiffening of the force constants arising from structural relaxations. In addition, the 170 cm(-1) mode is also found to become sharp at elevated temperatures. As the reduced spectra represent the vibrational density of states, the changes in the intensities of the 750 and 946 cm(-1) mode also suggest redistribution of density of states due to structural relaxations. (C) 2012 Elsevier By. All rights reserved.
引用
收藏
页码:99 / 104
页数:6
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