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Journal ArticleDOI

Electronic Polarizabilities of Ions in Crystals

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TLDR
In this paper, a set of electronic polarizabilities has been obtained from a least-squares fit of experimental refraction data using simple additivity and a Lorentz factor of $\frac{4\ensuremath{\pi}}{3}$.
Abstract
A set of electronic polarizabilities has been obtained from a least-squares fit of experimental refraction data using simple additivity and a Lorentz factor of $\frac{4\ensuremath{\pi}}{3}$. Except for the fluorides, the electronic polarizability values of the alkali-halide crystals calculated from this set agree with the experimental data within 3 percent. Similar least-squares fits were attempted with various values of the Lorentz factor, the best fit being obtained for $\frac{4\ensuremath{\pi}}{3}$. On the basis of $\frac{4\ensuremath{\pi}}{3}$, the additivity assumption and the alkali-halide set, polarizabilities have been obtained for other ions. The best values for the sodium $D$ line in ${\mathrm{A}}^{3}$ are ${\mathrm{Li}}^{+}$ 0.03, ${\mathrm{Na}}^{+}$ 0.41, ${\mathrm{K}}^{+}$ 1.33, ${\mathrm{Rb}}^{+}$ 1.98, ${\mathrm{Cs}}^{+}$ 3.34, ${\mathrm{F}}^{\ensuremath{-}}$ 0.64, ${\mathrm{Cl}}^{\ensuremath{-}}$ 2.96, ${\mathrm{Br}}^{\ensuremath{-}}$ 4.16, ${\mathrm{I}}^{\ensuremath{-}}$ 6.43, ${\mathrm{Ca}}^{++}$ 1.1, ${\mathrm{Sr}}^{++}$ 1.6, ${\mathrm{Ba}}^{++}$ 2.5, ${\mathrm{O}}^{\ensuremath{-}\ensuremath{-}}$ 0.5-3.2, ${\mathrm{S}}^{\ensuremath{-}\ensuremath{-}}$ 4.8-5.9, ${\mathrm{Se}}^{\ensuremath{-}\ensuremath{-}}$ 6.0-7.5, ${\mathrm{Te}}^{\ensuremath{-}\ensuremath{-}}$ 8.3-10.2, ${\mathrm{Ag}}^{+}$ 2.4, ${\mathrm{Cu}}^{+}$ 1.6, ${\mathrm{Cu}}^{++}$ 0.2, ${\mathrm{Zn}}^{++}$ 0.8, ${\mathrm{Cd}}^{++}$ 1.8, ${\mathrm{Ge}}^{4+}$ 1, ${\mathrm{Sn}}^{4+}$ 3.4, ${\mathrm{Pb}}^{++}$ 4.9. Values represented by a spread indicate ions that cannot be treated additively.

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Journal ArticleDOI

Dielectric polarizabilities of ions in oxides and fluorides

TL;DR: A set of 61 ion polarizabilities has been derived from the dielectric constants of 129 oxides and 25 fluorides using a least squares refinement technique in conjunction with the Clausius-Mosotti equation as mentioned in this paper.
Journal ArticleDOI

The Hofmeister effect and the behaviour of water at interfaces.

TL;DR: The first general, detailed qualitative molecular mechanism for the origins of ion-specific (Hofmeister) effects on the surface potential difference at an air-water interface is proposed; this mechanism suggests a simple model for the behaviour of water at all interfaces, regardless of whether the non-aqueous component is neutral or charged, polar or non-polar.
Book ChapterDOI

Cohesion of Ionic Solids in the Born Model

TL;DR: The Born model was originally proposed for the purpose of evaluating the lattice energy of crystals, which approach this idealized picture, and because of its success and simplicity it has subsequently been applied to the description of a variety of physical properties of ionic crystals, with varying degrees of success.
Journal ArticleDOI

Ionic sizes and born repulsive parameters in the NaCl-type alkali halides—II: The generalized Huggins-Mayer form☆

TL;DR: In this article, a generalized Huggins-Mayer form for the Born repulsive energy is adopted, and the resulting values of the crystal radii agree within 0·05 A with the values obtained in I with the Huggin-Mayers and Pauling forms.
Journal ArticleDOI

An interpretation of glass chemistry in terms of the optical basicity concept

TL;DR: In this article, the basicity of an oxide glass can be measured experimentally from the frequency shifts in the ultra-violet (UV) (s-p) spectra of probe ions such as Pb2+ and can be expressed on the numerical scale of optical basicity Λ (ideally Λ lies between zero and unity).