Raman scattering and Boson peaks in glasses: temperature and pressure effects

被引:84
作者
Schroeder, J
Wu, WM
Apkarian, JL
Lee, M
Hwa, LG
Moynihan, CT
机构
[1] Rensselaer Polytech Inst, Dept Phys Appl Phys & Astron, Troy, NY 12180 USA
[2] Yonsei Univ, Seoul 120749, South Korea
[3] Fu Jen Catholic Univ, Dept Phys, Taipei 24205, Taiwan
[4] Rensselaer Polytech Inst, Dept Math Sci, Troy, NY 12180 USA
关键词
D O I
10.1016/j.jnoncrysol.2004.08.265
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
Inelastic light scattering as a function of temperature and pressure was carried out on various oxide and halide glasses. For the low frequency Raman spectra, all of our glasses show a broad feature in the frequency range from 20 to 110 cm(-1) (0.60-3.30 THz); the 'Boson peak'. This Boson peak is associated with the existence of intermediate range order (IRO) in glass. The Boson peak is due to an increase in the vibrational density of states, over the Debye value, caused by localized excitations (phonon localizations). The low frequency Raman scattering containing this dominant spectral line (Boson peak) is interpreted in terms of its relationship to the amplitude and extent of the density fluctuations in glasses and is, thereby, considered a measure of the intermediate range order in these glasses. Phonon localization (the Ioffe-Regel criterion) was used to calculate correlation lengths for the measured glass samples. Characteristic correlation lengths for the glasses in this study were in the range of about 2-5 nanometer in size. We found that the Boson peak energies are highly pressure dependent but show very little change with temperature. The pressure effects in the Raman spectra will be discussed in terms of existing theories. The concept of intermediate range order (IRO) in glass and its applications will also be discussed. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:88 / 97
页数:10
相关论文
共 69 条
[1]   LOW-FREQUENCY RAMAN-SCATTERING AND STRUCTURE OF AMORPHOUS POLYMERS - STRETCHING EFFECT [J].
ACHIBAT, T ;
BOUKENTER, A ;
DUVAL, E ;
LORENTZ, G ;
ETIENNE, S .
JOURNAL OF CHEMICAL PHYSICS, 1991, 95 (04) :2949-2954
[2]   ON TEMPERATURE DEPENDENCE OF COOPERATIVE RELAXATION PROPERTIES IN GLASS-FORMING LIQUIDS [J].
ADAM, G ;
GIBBS, JH .
JOURNAL OF CHEMICAL PHYSICS, 1965, 43 (01) :139-&
[3]   'Strong' and 'superstrong' liquids, and an approach to the perfect glass state via phase transition [J].
Angell, CA ;
Moynihan, CT ;
Hemmati, M .
JOURNAL OF NON-CRYSTALLINE SOLIDS, 2000, 274 (1-3) :319-331
[4]   Evidence of high frequency propagating modes in vitreous silica [J].
Benassi, P ;
Krisch, M ;
Masciovecchio, C ;
Mazzacurati, V ;
Monaco, G ;
Ruocco, G ;
Sette, F ;
Verbeni, R .
PHYSICAL REVIEW LETTERS, 1996, 77 (18) :3835-3838
[5]   DISORDER-INDUCED LIGHT-SCATTERING IN SOLIDS - THE ORIGIN OF THE BOSON PEAK IN GLASSES [J].
BENASSI, P ;
FONTANA, A ;
FRIZZERA, W ;
MONTAGNA, M ;
MAZZACURATI, V ;
SIGNORELLI, G .
PHILOSOPHICAL MAGAZINE B-PHYSICS OF CONDENSED MATTER STATISTICAL MECHANICS ELECTRONIC OPTICAL AND MAGNETIC PROPERTIES, 1995, 71 (04) :761-769
[6]   DEFECT DIFFUSION AND A 2-FLUID MODEL FOR STRUCTURAL RELAXATION NEAR THE GLASS LIQUID TRANSITION [J].
BENDLER, JT ;
SHLESINGER, MF .
JOURNAL OF PHYSICAL CHEMISTRY, 1992, 96 (10) :3970-3973
[7]  
BILODEAU T, 1990, THESIS RENSSELAER PO
[8]  
BOHMER R, 1994, DISORDER EFFECTS ON RELAXATIONAL PROCESSES, P11
[9]   EXCESS OF LOW-ENERGY EXCITATIONS IN GLASSES [J].
CARINI, G ;
DANGELO, G ;
TRIPODO, G ;
FONTANA, A ;
LEONARDI, A ;
SAUNDERS, GA ;
BRODIN, A .
PHYSICAL REVIEW B, 1995, 52 (13) :9342-9353
[10]   NON-DEBYE AND NON-ARRHENIUS PRIMARY RESPONSE OF LIQUIDS, GLASSES, POLYMERS AND CRYSTALS [J].
CHAMBERLIN, RV ;
KINGSBURY, DW .
JOURNAL OF NON-CRYSTALLINE SOLIDS, 1994, 172 :318-326