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Fast ionic transport in AgxTiS2

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TLDR
In this article, the enthalpy of the subsystem of silver ions in the intercalation compounds Ag x TiS2 has been calculated from the electrochemically measured thermodynamic functions of the silver subsystem.
Abstract
The enthalpy of the subsystem of silver ions in the intercalation compounds Ag x TiS2 has been calculated from the electrochemically measured thermodynamic functions of the silver subsystem. The ionic conductivity and the coupled chemical diffusion coefficients for silver in the intercalation compound have been measured. The activation energy for diffusion of silver ions is determined and the obtained value is interpreted from analyzing the concentration dependence of the enthalpy of the ionic subsystem. The conclusion has been drawn that the high diffusion mobility is associated with the competition between the covalent and elastic interactions, which decreases the activation energy for diffusion of ions.

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Silver intercalation in SPS dense TiS2: staging and thermoelectric properties.

TL;DR: A decrease in electrical resistivity and the absolute value of the Seebeck coefficient with increasing Ag content supports also the charge transfer to the Ti 3d conduction band, enhancing the power factor in the specific temperature range.
Journal ArticleDOI

Chemical bond in FexTiSe2 intercalation compounds: dramatic influence of Fe concentration

TL;DR: In this paper, the influence of the iron concentration on the crystal structure, electronic structure and chemical bond in the FexTiSe2 intercalation compounds is studied across a wide composition range (0 ≤ x ≤ 0.50) within the homogeneous region of the system.
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Kinetics of reactions in interlayer space of titanium diselenide intercalated with iron

TL;DR: The hierarchy of diffusion mobilities of various defects in FexTiSe2 intercalation compound has been determined in this article, and it has been found that the largest mobility is inherent to intrinsic defects of the TiSe2 lattice, i.e., vacancies in Ti and Se sublattices.
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Influence of heterovalent substitution in the titanium sublattice on the electrochemical intercalation of lithium in M y Ti 1- y Se 2 ( M = Cr, V))

TL;DR: In this article, the influence of heterovalent substitutions on the electrochemical intercalation of lithium into titanium diselenide has been investigated, and it has been found that both types of doping insignificantly decrease the electromotive force with respect to metallic lithium.
Journal ArticleDOI

Synthesis, structure and properties of the layered CuxTiS2 compounds

TL;DR: In this article, a low-temperature layered phase CuxTiS2 (0.5, 0.3 and 0.7) has been prepared and the occupation of both octahedral and tetrahedral sites by the copper atoms in the interlayer gap of the TiS2 lattice is revealed.
References
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Journal ArticleDOI

On the Electrical Conductivity of Cuprous Sulfide: A Diffusion Theory

TL;DR: Theoretical expressions for the potential distributions for the process of tending to the limiting stationary state as well as for the stationary state were derived for the residual potential, a potential which remains after the current has been switched off and decays according as the initial homogeneity is recovered as discussed by the authors.
Journal ArticleDOI

Elastic energy and staging in intercalation compounds

TL;DR: In this paper, a simple model for the elastic energy associated with the intercalation of a layered host lattice is presented, which accounts for the staging phenomena observed in many intercalations systems and is compared with Safran's theory of staging.
Journal ArticleDOI

Structure and electrochemical properties of intercalation compounds in the system silver-titanium disulfide, Agx TiS2

TL;DR: In this paper, a superstructure due to three-dimensional order of silver, a √ 3 × 3 × 2c, space group P 3 1 c, is present below Tc = 301 K, where the transition to the disordered substructure, a = 3.428, c = 6.398 A, is of second-order nature.
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