scholarly journals Optical Properties of Alkali Halides in Ultraviolet Spectral Regions

Optics ◽  
2019 ◽  
Vol 1 (1) ◽  
pp. 18-31 ◽  
Author(s):  
Khagendra P. Bhandari

The optical reflectance spectra of alkali halide crystals KI and RbI were measured over the energy range of 4.14 to 6.91 eV. Both single crystal and poly-crystal samples were used to accomplish this task. The phase θ ( ω ) was computed using the Kramers-Kronig relation between the real and imaginary parts of the complex function, ln r = ln | r | + i θ ( ω ) . Subsequently, the optical constants n and κ were determined from the Fresnel reflectivity equation. The real and imaginary parts of dielectric constants ε 1 and ε 2 were then calculated using n and κ. The optical absorption spectra of the crystal have also been measured in these spectral regions. The spectra agree reasonably well with the current theory concerning exciton peaks. In addition, a shoulder was found in the spectra similar to those previously seen and associated with the band-to-band transition in the alkali iodides.

1974 ◽  
Vol 29 (11) ◽  
pp. 1601-1607
Author(s):  
K. D. Misra ◽  
V. K. Dixit ◽  
M. N. Sharma

The appropriateness of a suitably modified Varshni-Shukla potential has been tested for a series of alkali halide crystals by determining the numerical values of the potential parameters involved, using Hildebrand’s equation of state and thereby computing a few lattice properties. Comparison between the different sets of theoretical and experimental results infers that the present theoretical values exhibit an improvement over those of other workers, using a similar approach but with different potential energy functions. It is concluded that the modified V -S potential function is a good choice for explaining the behaviour of alkali halide lattices.


1981 ◽  
Vol 59 (10) ◽  
pp. 1359-1366 ◽  
Author(s):  
Jai Shanker ◽  
T. S. Verma ◽  
A. Cox ◽  
M. J. L. Sangster

In order to make a critical test of some recently developed interionic potentials based on the shell model, the photoelastic behaviour of the alkali halide crystals has been investigated. Values of the strain derivatives of the static and high-frequency dielectric constants have been calculated from sets of potentials due to Catlow et al., Sangster et al., and Sangster and Atwood. A comparison of the results obtained with available experimental photoelastic data demonstrates the superiority of the second set of potentials of Catlow et al.


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.


1975 ◽  
Vol 53 (2) ◽  
pp. 192-199 ◽  
Author(s):  
Taiju Tsuboi ◽  
K. Oyama ◽  
P. W. M. Jacobs

A systematic investigation of the line shape of the A band of several ions with the s2 configuration dissolved in alkali halides has been made on KCl:In+, KBr:In+, KCl:Sn2+, KBr:Sn2+, KI:Sn2+, RbCl:Sn2+, KCl:Tl+, KBr:Tl+, KI:Tl+, and KBr:Pb2+ crystals. A temperature sensitive doublet structure was observed for In+ and Sn2+ doped crystals and for KCl:Tl+, while a single band, which is asymmetric at high temperatures, was observed for KBr:Tl+ and KBr:Pb2+. The temperature dependence of the line shape supports Toyozawa and Inoue's theory in which the fine structure is ascribed to the dynamical Jahn–Teller effect. A discussion is given of the importance of quadratic electron–lattice interaction and its effect on the asymmetry of the line shape.


1958 ◽  
Vol 112 (1) ◽  
pp. 90-103 ◽  
Author(s):  
B. G. Dick ◽  
A. W. Overhauser

Author(s):  
W. Kucharczyk

AbstractA simple model of the quadratic transverse electrostrictive effect in alkali halide crystals with the NaCl structure is considered. Two contributions to the transverse coefficient are taken into account. The first term is due to the relative displacement of the negative and positive ions. The second one is related to the coupling of transverse and longitudinal deformation.


Sign in / Sign up

Export Citation Format

Share Document