NMR study of AgInTe$_2$ at normal and high pressure

Fuente: arXiv
Guardado en:
Detalles Bibliográficos
Autores principales: Guehne, Robin, Kattinger, Carsten, Bertmer, Marko, Welzmiller, Simon, Oeckler, Oliver, Haase, Jürgen
Formato: Preprint
Publicado: 2022
Materias:
Acceso en línea:
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
_version_ 1866929520924164096
author Guehne, Robin
Kattinger, Carsten
Bertmer, Marko
Welzmiller, Simon
Oeckler, Oliver
Haase, Jürgen
author_facet Guehne, Robin
Kattinger, Carsten
Bertmer, Marko
Welzmiller, Simon
Oeckler, Oliver
Haase, Jürgen
contents The ternary semiconductor AgInTe$_2$ is a thermoelectric material with chalcopyrite-type structure that transforms reversibly into a rocksalt-type structure under high pressure. Nuclear magnetic resonance (NMR) is considered to provide unique insight into material properties on interatomic length scales, especially in the context of structural phase transitions. Here, $^{115}$In and $^{125}$Te NMR is used to study AgInTe$_2$ for ambient conditions and pressures up to 5 GPa. Magnetic field dependent and magic angle spinning (MAS) experiments of $^{125}$Te prove strongly enhanced internuclear couplings, as well as a distribution of isotropic chemical shifts suggesting a certain degree of cation disorder. The indirect nuclear coupling is smaller for $^{115}$In, as well as the chemical shift distribution in agreement with the crystal structure. The $^{115}$In NMR is further governed by a small quadrupolar interaction ($ν_\mathrm{Q} \approx$ 90 kHz) and shows an orders of magnitude faster nuclear relaxation in comparison to that of $^{125}$Te. At a pressure of about 3 GPa, the $^{115}$In quadrupole interaction increases sharply to about 2400 kHz, indicating a phase transition to a structure with a well defined, though non-cubic local symmetry, while the $^{115}$In shift suggests no significant changes of the electronic structure. The NMR signal is lost above about 5 GPa (at least up to about 10 GPa). However, upon releasing the pressure a signal is recovered that points to the reported metastable ambient pressure phase with a high degree of disorder.
format Preprint
id arxiv_https___arxiv_org_abs_2201_13116
institution arXiv
publishDate 2022
record_format arxiv
spellingShingle NMR study of AgInTe$_2$ at normal and high pressure
Guehne, Robin
Kattinger, Carsten
Bertmer, Marko
Welzmiller, Simon
Oeckler, Oliver
Haase, Jürgen
Materials Science
The ternary semiconductor AgInTe$_2$ is a thermoelectric material with chalcopyrite-type structure that transforms reversibly into a rocksalt-type structure under high pressure. Nuclear magnetic resonance (NMR) is considered to provide unique insight into material properties on interatomic length scales, especially in the context of structural phase transitions. Here, $^{115}$In and $^{125}$Te NMR is used to study AgInTe$_2$ for ambient conditions and pressures up to 5 GPa. Magnetic field dependent and magic angle spinning (MAS) experiments of $^{125}$Te prove strongly enhanced internuclear couplings, as well as a distribution of isotropic chemical shifts suggesting a certain degree of cation disorder. The indirect nuclear coupling is smaller for $^{115}$In, as well as the chemical shift distribution in agreement with the crystal structure. The $^{115}$In NMR is further governed by a small quadrupolar interaction ($ν_\mathrm{Q} \approx$ 90 kHz) and shows an orders of magnitude faster nuclear relaxation in comparison to that of $^{125}$Te. At a pressure of about 3 GPa, the $^{115}$In quadrupole interaction increases sharply to about 2400 kHz, indicating a phase transition to a structure with a well defined, though non-cubic local symmetry, while the $^{115}$In shift suggests no significant changes of the electronic structure. The NMR signal is lost above about 5 GPa (at least up to about 10 GPa). However, upon releasing the pressure a signal is recovered that points to the reported metastable ambient pressure phase with a high degree of disorder.
title NMR study of AgInTe$_2$ at normal and high pressure
topic Materials Science
url https://arxiv.org/abs/2201.13116