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Wyświetlanie 1-2 z 2
Tytuł:
Physics of Neutral-to-Ionic Phase Transition in Organic Charge Transfer Semiconducting Compounds
Autorzy:
Cailleau, H.
Lemée-Cailleau, M. H.
Le Cointe, M.
Luty, T.
Powiązania:
https://bibliotekanauki.pl/articles/1967953.pdf
Data publikacji:
1997-10
Wydawca:
Polska Akademia Nauk. Instytut Fizyki PAN
Tematy:
71.38.+i
61.50.Ks
71.35.Aa
Opis:
An uncommon excitonic instability takes place in some exotic semiconducting compounds. Indeed, the equilibrium neutral-to-ionic (N-I) phase transition, as well as the non-equilibrium photo-induced phase transformation, observed in some organic charge-transfer complexes, originate from intra- and inter-chain cooperative effects between structurally relaxed charge-transfer excitations. This electronic-structural phase transition manifests itself by a change of the degree of charge-transfer and a dimerization distortion with the formation of donor-acceptor pairs along the stacking axis in the I phase. Thermal charge-transfer excitations associated with the formation of I strings along N chains are at the heart of the mechanism of this phase transition. These relaxed electronic excitations, which are an intrinsic feature of low-dimensional systems with strong electron-phonon coupling, can be described in terms of self-trapping and self-multiplication of charge-transfer excitons. Precise structural studies on the prototype compound, tetrathiafulvalene-p-chloranil allow to highlight the respective role taken by the ionicity and the dimerization. Symmetry and thermodynamics analysis of the N-I transition, based on recent determination of the pressure-temperature phase diagram, make possible to present a consistent picture of this phase transition. Supported by theoretical considerations taking into account the interplay between quantum and thermal effects, the experimental observations show that the N-I transition results from the condensation and the ordering (crystallization) of charge-transfer excitations, following a phase diagram analogous to the solid-liquid-gas one.
Źródło:
Acta Physica Polonica A; 1997, 92, 4; 597-608
0587-4246
1898-794X
Pojawia się w:
Acta Physica Polonica A
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
High-Pressure Study of $Gd_2(MoO_4)_3$ by Raman Scattering and Ab Initio Calculations
Autorzy:
Lucazeau, G.
Bouvier, P.
Pasturel, A.
Le Bacq, O.
Pagnier, T.
Powiązania:
https://bibliotekanauki.pl/articles/1807798.pdf
Data publikacji:
2009-07
Wydawca:
Polska Akademia Nauk. Instytut Fizyki PAN
Tematy:
61.50.Ks
64.70.K-
71.15.Mb
78.30.-j
Opis:
High-pressure induced phase transitions in a single crystal of gadolinium molybdate, $Gd_2(MoO_4)_3$ were studied by the Raman spectroscopy and ab initio calculations. The amorphization of the sample takes place at about 6 GPa in a mixture of alcohol as a pressure transmitting medium and begins as soon as 3 GPa in argon. In both media, the amorphization is irreversible in the 0-9 GPa investigated pressure range. The joint ab initio and Raman results allowed us to conclude that rotations of $MoO_4$ tetrahedra are the primary structural changes involved in the first phase transition (at about 2 GPa) explaining the softening of the low frequency modes at about 50 $cm^{-1}$. In addition, a progressive distortion of tetrahedra followed by a coordination change (IV-VI) of Mo atoms is observed through the five structural transitions including amorphization. This mechanism based on the steric hindrance of polyhedra is believed to be the most relevant for explaining the amorphization of $Gd_2(MoO_4)_3$.
Źródło:
Acta Physica Polonica A; 2009, 116, 1; 25-31
0587-4246
1898-794X
Pojawia się w:
Acta Physica Polonica A
Dostawca treści:
Biblioteka Nauki
Artykuł
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