Low frequency vibrational modes and phase transitions in mixed perovskite ferroelectrics

1978 ◽  
Vol 21 (1) ◽  
pp. 555-556 ◽  
Author(s):  
D. Bäuerle
1994 ◽  
Vol 269 (49) ◽  
pp. 31047-31050
Author(s):  
S Jeyarajah ◽  
L M Proniewicz ◽  
H Bronder ◽  
J R Kincaid

Soft Matter ◽  
2021 ◽  
Author(s):  
Brian Tighe ◽  
Karsten Baumgarten

We determine how low frequency vibrational modes control the elastic shear modulus of Mikado networks, a minimal mechanical model for semi-flexible fiber networks. From prior work it is known that...


1995 ◽  
Vol 398 ◽  
Author(s):  
A.R. Guo ◽  
C.-S. Tu ◽  
Ruiwu Tao ◽  
R.S. Katiyar ◽  
Ruyan Guo ◽  
...  

ABSTRACTThe longitudinal (LO) and transverse (TO) A1 vibrational modes have been measured between 30-1200 cm−1 as a function of temperature (30–1240 K) for CsTiOAsO4 (CTA). The frequencies for all corresponding Raman components shifted to lower frequencies on increasing the temperature, however, there is no typical soft-mode like behavior observed in the measured frequency range. The relative intensities of the low frequency bands increase dramatically with increasing temperature due to high mobility of Cs+ ion. A higher symmetry structure taking place above 940K has been confirmed by changes in the phonon spectra.


2017 ◽  
Vol 114 (46) ◽  
pp. E9767-E9774 ◽  
Author(s):  
Hideyuki Mizuno ◽  
Hayato Shiba ◽  
Atsushi Ikeda

The low-frequency vibrational and low-temperature thermal properties of amorphous solids are markedly different from those of crystalline solids. This situation is counterintuitive because all solid materials are expected to behave as a homogeneous elastic body in the continuum limit, in which vibrational modes are phonons that follow the Debye law. A number of phenomenological explanations for this situation have been proposed, which assume elastic heterogeneities, soft localized vibrations, and so on. Microscopic mean-field theories have recently been developed to predict the universal non-Debye scaling law. Considering these theoretical arguments, it is absolutely necessary to directly observe the nature of the low-frequency vibrations of amorphous solids and determine the laws that such vibrations obey. Herein, we perform an extremely large-scale vibrational mode analysis of a model amorphous solid. We find that the scaling law predicted by the mean-field theory is violated at low frequency, and in the continuum limit, the vibrational modes converge to a mixture of phonon modes that follow the Debye law and soft localized modes that follow another universal non-Debye scaling law.


2002 ◽  
Vol 12 (9) ◽  
pp. 149-152
Author(s):  
S. Brazovskii

Recently the ferroelectric FE anomaly (Nad, Monceau, et al.) followed by the charge disproportionation CD (Brown, et al) have been discovered in ($TMTTF)_2X$ compounds. A theory of the combined Mott-Hubbard state describes both effects by interference of the build-in nonequivalence of bonds and the spontaneous one of sites. The state gives rise to three types of solitons: $\pi -$ solitons (holons) are observed via the activation energy A in conductivity G; noninteger $\alpha -$ solitons provide the frequency dispersion of the FE response; combined spin-charge solitons determine $G(T)$ below subsequent phase transitions. The optical edge lies well below the conductivity gap 2A; the critical FE mode coexists with a combined electron-phonon resonance and a phonon antiresonance. The CD and the FE can exists hiddenly even in the Se subfamily giving rise to the unexplained yet low frequency optical peak, the enhanced pseudogap and traces of phonons activation.


1975 ◽  
Vol 53 (9) ◽  
pp. 1247-1253 ◽  
Author(s):  
R. H. Wright ◽  
R. E. Burgess

An analysis of the low-frequency vibrational modes of organic compounds in 19 odor categories indicates that the primary process of olfactory stimulation is common to both vertebrates and insects. Understanding the molecular basis of olfactory specificity may provide a clue to the physiological mechanisms and has immediate practical applications in the control of insect pests.


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