Strain dependence of the low‐frequency dielectric constants of a few alkali halides

1983 ◽  
Vol 54 (5) ◽  
pp. 2875-2877 ◽  
Author(s):  
Geetha Balakrishnan ◽  
K. Srinivasan ◽  
R. Srinivasan
1992 ◽  
Vol 33 (5) ◽  
pp. 389-393 ◽  
Author(s):  
R.R. Reddy ◽  
S. Anjaneyulu ◽  
T.V.R. Rao

1969 ◽  
Vol 47 (17) ◽  
pp. 1757-1767 ◽  
Author(s):  
M. Buchanan ◽  
E. J. Woll Jr.

The calculation of vibronic side bands of defects in crystals is discussed. A model for the deformation of the lattice about a Sm2+ defect in alkali halides and side-band calculations on this model for KBr and KCl containing Sm2+ are compared with experimentally observed side bands. Improvements, particularly in the low frequency region, are found over the calculations assuming no deformation.


1973 ◽  
Vol 51 (4) ◽  
pp. 545-550 ◽  
Author(s):  
I. Lubezky ◽  
R. McIntosh

The dielectric constants and dielectric losses of solutions of nitrobenzene and 2,2,4-trimethyl pentane have been measured near the critical solution temperature over a concentration range of 22–75% by weight and in the frequency regions of 5–60 and 1000 – 4000 kHz. It was found that below a critical concentration of 35% maxima existed in ε′ and ε″ at a temperature of 0.3 °C above the critical solution temperature. At higher concentrations the maxima disappeared and phase separation was preceded only by changes in the thermal coefficients dε′/dT and dε″/dT. The present study combined with others indicates that two regions of loss exist for the system near the critical temperature: low frequency losses of a conductive nature and high frequency losses of the Debye type. The published experimental knowledge of such systems remains insufficient to enable a thorough test of the theoretical studies published recently by Snider.


1988 ◽  
Vol 66 (5) ◽  
pp. 385-389 ◽  
Author(s):  
S. K. Sharma ◽  
R. M. Misra ◽  
M. N. Sharma ◽  
M. P. Madan

A theoretical estimate of the high-frequency dielectric constants is made using the molar polarizabilities for a number of alkali halides. These are shown to be in good agreement with the new and more reliable experimental data. Analysis by means of the additivity rule within the family of salts is used to compute the total free ion polarizability of ionic constituents and the change in polarizability when the ions are placed in a crystalline environment. Furthermore, the anion electronic polarizability in ionic crystals has been determined. It is found to vary from crystal to crystal, as opposed to the generally accepted assumption that each ion has the same polarizability in all compounds. The dependence of polarizability upon ionic radii has been discussed. The results from this simple analysis compare well with other determinations.


2010 ◽  
Vol 645-648 ◽  
pp. 1203-1206
Author(s):  
Sergey Y. Davydov ◽  
Alexander A. Lebedev

Within the scope of the Harrison’s bond orbital model the spontaneous polarization, high- and low frequency dielectric constants are obtained in an analytical form. Theoretical results are in a reasonable agreement with the experimental data available and the numerical calculations based on the ab initio methods.


1966 ◽  
Vol 21 (3) ◽  
pp. 259-260 ◽  
Author(s):  
E. Bernal ◽  
G.D. Chen ◽  
T.C. Lee

1997 ◽  
Vol 493 ◽  
Author(s):  
M. J. Dalberth ◽  
J. C. Price ◽  
C. T. Rogers

ABSTRACTUsing pulsed laser ablation, we have grown epitaxial bilayers of strontium titanate (STO) and yttrium barium copper oxide (YBCO) on lanthanum aluminate (LAO) and neodymium gallate (NGO) substrates. Using a selective acid etch, we have removed the YBCO from the middle of the bilayer and lifted off the strontium titanate films from their parent substrates. Using coplanar interdigital capacitors patterned on the films' surface, we have measured the dielectric constant and loss as a function of frequency and temperature and have resolved frequency dependent loss peaks which indicate thermally activated behavior. Also, by applying a dc bias to the capacitor, we have seen tuning of the lifted off films' dielectric constants that compares favorably to films attached to substrates.


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