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Journal ArticleDOI

Theory of the Transition in KH2PO4

John C. Slater
- 01 Jan 1941 - 
- Vol. 9, Iss: 1, pp 16-33
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TLDR
In this paper, the theory of spontaneous polarization along the axis of the crystal, resulting in a well-known transition, similar to Rochelle salt, with polarization below the Curie point was worked out.
Abstract
Potassium dihydrogen phosphate contains phosphate groups connected by hydrogen bonds. Different possible arrangements of the hydrogens result effectively in different orientations of the (H2PO4)— dipoles. Since these have the lowest energy when pointing along the axis of the crystal, there is a tendency toward spontaneous polarization along this axis, resulting in the well‐known transition, similar to Rochelle salt, with polarization below the Curie point. The theory of this transition is worked out, using statistical methods to count the number of arrangements of hydrogens consistent with each total polarization of the crystal, and deriving the free energy. It is found that the theory predicts a phase change of the first order, with sudden transition from the polarized state at low temperature to the unpolarized state at high temperature, rather than the lambda‐point transition or phase change of the second order which is observed. However, the observed transition is confined to a very narrow temperature range compared to that predicted, for instance, by the Weiss theory, so that it seems as if it might be merely a broadened transition of the first order. It is suggested that the broadening may result from the irregular shifts of transition temperatures of individual domains in the crystal on account of stresses resulting from the large piezoelectric effect and the resulting deformation of the crystal below the transition point. The susceptibility above the Curie point comes out by the theory to be 4.33 times as great as it should according to the Weiss theory, a result which seems to be in general agreement with experiment. The entropy change in the transition is given by the theory as 0.69 unit, somewhat smaller than the observed value of about 0.8 unit. No explanation is suggested for this discrepancy.

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Citations
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Why Are There so Few Magnetic Ferroelectrics

TL;DR: In this paper, the fundamental physics behind the scarcity of ferromagnetic ferroelectric coexistence was explored and the properties of known magnetically ordered ferro-electric materials were examined.
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Theory of ferroelectrics

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Multiferroic Behavior Associated with an Order−Disorder Hydrogen Bonding Transition in Metal−Organic Frameworks (MOFs) with the Perovskite ABX3 Architecture

TL;DR: This research opens up a new class of multiferroics in which the electrical ordering is achieved by means of hydrogen bonding, and the compounds become canted weak ferromagnets below 40 K.
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Residual Entropy of Square Ice

TL;DR: In this article, the problem of finding the number of ways of drawing arrows on the bonds of a square planar net so that precisely two arrows point into each vertex was studied.
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Soft-mode spectroscopy: Experimental studies of structural phase transitions

TL;DR: In this article, the experimental studies of displacive phase transitions in solids are summarized, focusing on inelastic light scattering and neutron scattering; related infrared reflectivity measurements, as well as x-ray and EPR analyses are also summarized.
References
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Journal ArticleDOI

On the Role of Dipole‐Dipole Coupling in Dielectric Media

TL;DR: In this paper, the Clausius-Mossotti formula was used to explain the absence of spontaneous polarization, as well as the non-occurrence of much saturation curvature in strong applied fields.
Journal ArticleDOI

Piezoelektrizität von Kaliumphosphat

TL;DR: The Piezomodul d36 von Kaliumphosphatkristallen in seiner Abhangigkeit von der Temperatur statisch gemessen as discussed by the authors is also a substanz, and steigt er in der Nahe des seignette-elektrischen Curie-Punktes auserordentlich stark an und erreicht bei etwa 1230 abs.
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