Density Functional Theory Study of Lanthanide Monoxides under High Pressure: Pressure-Induced B1–B2 Transition

Autores
Ferrari, Sergio; Errandonea, Daniel
Año de publicación
2024
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Using density-functional theory we have studied the influence of hydrostatic pressure in the crystal structure of lanthanide monoxides considering the monoxides formed by the fifteen ele-ments of the lanthanide series, from La to Lu. Calculations have been performed using two methods for the ambient-pressure B1 (NaCl-type) structure, the general-gradient approximation (GGA) and the local-density approximation (LDA). By a systematic comparison with existent experimental data, we have found that the first method agrees better with experiments. In addi-tion, considering other cubic structures previously reported for lanthanide monoxides, as B2 (CsCl-type) and B3 (ZnS-type), we have explored the possibility of the occurrence of pres-sure-induced phase transitions. Based on the better accuracy of GGA to describe the B1 phase at ambient conditions, we have exclusively used GGA for the high-pressure study. We have found for the fifteen studied compounds that at ambient pressure the B1 structure is the one with the lowest enthalpy, being therefore the thermodynamically most stable structure. We have also determined that at elevated pressures all the studied compounds undergo a structural phase transition to the B2 phase. We have finally established the relationship between pressure and the volume of the unit cell, along with the associated isothermal equation of state, determining the bulk modulus.
Fil: Ferrari, Sergio. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Comisión Nacional de Energía Atómica. Gerencia del Área de Investigaciones y Aplicaciones no Nucleares. Gerencia de Física (Centro Atómico Constituyentes); Argentina
Fil: Errandonea, Daniel. Universidad de Valencia; España
Materia
Lanthanide monoxide
High pressure, phase transition
Density-functional theory
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/263338

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spelling Density Functional Theory Study of Lanthanide Monoxides under High Pressure: Pressure-Induced B1–B2 TransitionFerrari, SergioErrandonea, DanielLanthanide monoxideHigh pressure, phase transitionDensity-functional theoryhttps://purl.org/becyt/ford/1.3https://purl.org/becyt/ford/1Using density-functional theory we have studied the influence of hydrostatic pressure in the crystal structure of lanthanide monoxides considering the monoxides formed by the fifteen ele-ments of the lanthanide series, from La to Lu. Calculations have been performed using two methods for the ambient-pressure B1 (NaCl-type) structure, the general-gradient approximation (GGA) and the local-density approximation (LDA). By a systematic comparison with existent experimental data, we have found that the first method agrees better with experiments. In addi-tion, considering other cubic structures previously reported for lanthanide monoxides, as B2 (CsCl-type) and B3 (ZnS-type), we have explored the possibility of the occurrence of pres-sure-induced phase transitions. Based on the better accuracy of GGA to describe the B1 phase at ambient conditions, we have exclusively used GGA for the high-pressure study. We have found for the fifteen studied compounds that at ambient pressure the B1 structure is the one with the lowest enthalpy, being therefore the thermodynamically most stable structure. We have also determined that at elevated pressures all the studied compounds undergo a structural phase transition to the B2 phase. We have finally established the relationship between pressure and the volume of the unit cell, along with the associated isothermal equation of state, determining the bulk modulus.Fil: Ferrari, Sergio. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Comisión Nacional de Energía Atómica. Gerencia del Área de Investigaciones y Aplicaciones no Nucleares. Gerencia de Física (Centro Atómico Constituyentes); ArgentinaFil: Errandonea, Daniel. Universidad de Valencia; EspañaMultidisciplinary Digital Publishing Institute2024-09info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/263338Ferrari, Sergio; Errandonea, Daniel; Density Functional Theory Study of Lanthanide Monoxides under High Pressure: Pressure-Induced B1–B2 Transition; Multidisciplinary Digital Publishing Institute; Crystals; 14; 10; 9-2024; 1-122073-4352CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.mdpi.com/2073-4352/14/10/831info:eu-repo/semantics/altIdentifier/doi/10.3390/cryst14100831info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-22T11:46:10Zoai:ri.conicet.gov.ar:11336/263338instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-10-22 11:46:10.449CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Density Functional Theory Study of Lanthanide Monoxides under High Pressure: Pressure-Induced B1–B2 Transition
title Density Functional Theory Study of Lanthanide Monoxides under High Pressure: Pressure-Induced B1–B2 Transition
spellingShingle Density Functional Theory Study of Lanthanide Monoxides under High Pressure: Pressure-Induced B1–B2 Transition
Ferrari, Sergio
Lanthanide monoxide
High pressure, phase transition
Density-functional theory
title_short Density Functional Theory Study of Lanthanide Monoxides under High Pressure: Pressure-Induced B1–B2 Transition
title_full Density Functional Theory Study of Lanthanide Monoxides under High Pressure: Pressure-Induced B1–B2 Transition
title_fullStr Density Functional Theory Study of Lanthanide Monoxides under High Pressure: Pressure-Induced B1–B2 Transition
title_full_unstemmed Density Functional Theory Study of Lanthanide Monoxides under High Pressure: Pressure-Induced B1–B2 Transition
title_sort Density Functional Theory Study of Lanthanide Monoxides under High Pressure: Pressure-Induced B1–B2 Transition
dc.creator.none.fl_str_mv Ferrari, Sergio
Errandonea, Daniel
author Ferrari, Sergio
author_facet Ferrari, Sergio
Errandonea, Daniel
author_role author
author2 Errandonea, Daniel
author2_role author
dc.subject.none.fl_str_mv Lanthanide monoxide
High pressure, phase transition
Density-functional theory
topic Lanthanide monoxide
High pressure, phase transition
Density-functional theory
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.3
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv Using density-functional theory we have studied the influence of hydrostatic pressure in the crystal structure of lanthanide monoxides considering the monoxides formed by the fifteen ele-ments of the lanthanide series, from La to Lu. Calculations have been performed using two methods for the ambient-pressure B1 (NaCl-type) structure, the general-gradient approximation (GGA) and the local-density approximation (LDA). By a systematic comparison with existent experimental data, we have found that the first method agrees better with experiments. In addi-tion, considering other cubic structures previously reported for lanthanide monoxides, as B2 (CsCl-type) and B3 (ZnS-type), we have explored the possibility of the occurrence of pres-sure-induced phase transitions. Based on the better accuracy of GGA to describe the B1 phase at ambient conditions, we have exclusively used GGA for the high-pressure study. We have found for the fifteen studied compounds that at ambient pressure the B1 structure is the one with the lowest enthalpy, being therefore the thermodynamically most stable structure. We have also determined that at elevated pressures all the studied compounds undergo a structural phase transition to the B2 phase. We have finally established the relationship between pressure and the volume of the unit cell, along with the associated isothermal equation of state, determining the bulk modulus.
Fil: Ferrari, Sergio. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Comisión Nacional de Energía Atómica. Gerencia del Área de Investigaciones y Aplicaciones no Nucleares. Gerencia de Física (Centro Atómico Constituyentes); Argentina
Fil: Errandonea, Daniel. Universidad de Valencia; España
description Using density-functional theory we have studied the influence of hydrostatic pressure in the crystal structure of lanthanide monoxides considering the monoxides formed by the fifteen ele-ments of the lanthanide series, from La to Lu. Calculations have been performed using two methods for the ambient-pressure B1 (NaCl-type) structure, the general-gradient approximation (GGA) and the local-density approximation (LDA). By a systematic comparison with existent experimental data, we have found that the first method agrees better with experiments. In addi-tion, considering other cubic structures previously reported for lanthanide monoxides, as B2 (CsCl-type) and B3 (ZnS-type), we have explored the possibility of the occurrence of pres-sure-induced phase transitions. Based on the better accuracy of GGA to describe the B1 phase at ambient conditions, we have exclusively used GGA for the high-pressure study. We have found for the fifteen studied compounds that at ambient pressure the B1 structure is the one with the lowest enthalpy, being therefore the thermodynamically most stable structure. We have also determined that at elevated pressures all the studied compounds undergo a structural phase transition to the B2 phase. We have finally established the relationship between pressure and the volume of the unit cell, along with the associated isothermal equation of state, determining the bulk modulus.
publishDate 2024
dc.date.none.fl_str_mv 2024-09
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/263338
Ferrari, Sergio; Errandonea, Daniel; Density Functional Theory Study of Lanthanide Monoxides under High Pressure: Pressure-Induced B1–B2 Transition; Multidisciplinary Digital Publishing Institute; Crystals; 14; 10; 9-2024; 1-12
2073-4352
CONICET Digital
CONICET
url http://hdl.handle.net/11336/263338
identifier_str_mv Ferrari, Sergio; Errandonea, Daniel; Density Functional Theory Study of Lanthanide Monoxides under High Pressure: Pressure-Induced B1–B2 Transition; Multidisciplinary Digital Publishing Institute; Crystals; 14; 10; 9-2024; 1-12
2073-4352
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/https://www.mdpi.com/2073-4352/14/10/831
info:eu-repo/semantics/altIdentifier/doi/10.3390/cryst14100831
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Multidisciplinary Digital Publishing Institute
publisher.none.fl_str_mv Multidisciplinary Digital Publishing Institute
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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