Phase Transformation in Lithium Niobate-Lithium Tantalate Solid Solutions (LiNb$_{1-x}$Ta$_x$O$_3$)

Fuente: arXiv
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Autores principales: Azzouzi, Fatima El, Klimm, Detlef, Kapp, Alexander, Verhoff, Leonard M., Schäfer, Nils A., Ganschow, Steffen, Becker, Klaus-Dieter, Sanna, Simone, Fritze, Holger
Formato: Preprint
Publicado: 2024
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author Azzouzi, Fatima El
Klimm, Detlef
Kapp, Alexander
Verhoff, Leonard M.
Schäfer, Nils A.
Ganschow, Steffen
Becker, Klaus-Dieter
Sanna, Simone
Fritze, Holger
author_facet Azzouzi, Fatima El
Klimm, Detlef
Kapp, Alexander
Verhoff, Leonard M.
Schäfer, Nils A.
Ganschow, Steffen
Becker, Klaus-Dieter
Sanna, Simone
Fritze, Holger
contents The investigation of the structural phase transition in the vicinity of the Curie temperature $T_c$ of LiNb$_{1-x}$Ta$_x$O$_3$ crystals is motivated by the expected combination of advantageous high-temperature properties of LiNbO$_3$ and LiTaO$_3$, including high piezoelectric modules and remarkable high-temperature stability, respectively. $T_c$ marks the ultimate limit for exploiting the piezoelectric properties, however transition related structural modifications might impact this and other properties even below $T_c$. Remarkably, the phase transition from the ferroelectric to the paraelectric phase, whose temperature strongly depends on the composition $x$, shows a significant drop in the activation energy of the electrical conductivity. The magnitude, temperature dependence and underlying mechanisms of this drop are discussed from a microscopic perspective. Molecular dynamics calculations in the framework of the density functional theory show that substantial displacements of the cations occur below $T_c$ for both the end compounds LiNbO$_3$ and LiTaO$_3$, and might thus affect the electrical conductivity. Above $T_c$, the migration of lithium ions is presumably facilitated by a shortened diffusion path for the most favorable jump of the lithium ions. Electronic contributions to the conductivity, which become important above 900 K, are explained within the polaronic picture by the formation and migration of free small polarons.
format Preprint
id arxiv_https___arxiv_org_abs_2403_16717
institution arXiv
publishDate 2024
record_format arxiv
spellingShingle Phase Transformation in Lithium Niobate-Lithium Tantalate Solid Solutions (LiNb$_{1-x}$Ta$_x$O$_3$)
Azzouzi, Fatima El
Klimm, Detlef
Kapp, Alexander
Verhoff, Leonard M.
Schäfer, Nils A.
Ganschow, Steffen
Becker, Klaus-Dieter
Sanna, Simone
Fritze, Holger
Materials Science
The investigation of the structural phase transition in the vicinity of the Curie temperature $T_c$ of LiNb$_{1-x}$Ta$_x$O$_3$ crystals is motivated by the expected combination of advantageous high-temperature properties of LiNbO$_3$ and LiTaO$_3$, including high piezoelectric modules and remarkable high-temperature stability, respectively. $T_c$ marks the ultimate limit for exploiting the piezoelectric properties, however transition related structural modifications might impact this and other properties even below $T_c$. Remarkably, the phase transition from the ferroelectric to the paraelectric phase, whose temperature strongly depends on the composition $x$, shows a significant drop in the activation energy of the electrical conductivity. The magnitude, temperature dependence and underlying mechanisms of this drop are discussed from a microscopic perspective. Molecular dynamics calculations in the framework of the density functional theory show that substantial displacements of the cations occur below $T_c$ for both the end compounds LiNbO$_3$ and LiTaO$_3$, and might thus affect the electrical conductivity. Above $T_c$, the migration of lithium ions is presumably facilitated by a shortened diffusion path for the most favorable jump of the lithium ions. Electronic contributions to the conductivity, which become important above 900 K, are explained within the polaronic picture by the formation and migration of free small polarons.
title Phase Transformation in Lithium Niobate-Lithium Tantalate Solid Solutions (LiNb$_{1-x}$Ta$_x$O$_3$)
topic Materials Science
url https://arxiv.org/abs/2403.16717