Destabilization of the LiNH2–LiH hydrogen storage system by aluminum incorporation
- Autores
- Fernández Albanesi, Luisa Francisca; Arneodo Larochette, Pierre Paul; Gennari, Fabiana Cristina
- Año de publicación
- 2013
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- The lithium amide–lithium hydride system (LiNH2–LiH) is one of the most attractive light-weight materials for hydrogen storage. In an effort to improve its hydrogen sorption kinetics, the effect of 1 mol% AlCl3 addition to LiNH2–LiH system was systematically investigated by differential scanning calorimetry, X-ray diffraction, Fourier transform infrared analysis and hydrogen volumetric measurements. It is shown that Al3+ is incorporated into the LiNH2 structure by partial substitution of Li+ forming a new amide in the Li–Al–N–H system, which is reversible under hydriding/dehydriding cycles. This new substituted amide displays improved hydrogen storage properties with respect to LiNH2–LiH. In fact, a stable hydrogen storage capacity of about 4.5–5.0 wt% is observed under cycling and is completely desorbed in 30 min at 275 °C for the Li–Al–N–H system. Moreover, the concurrent incorporation of Al3+ and the presence of LiH are effective for mitigating the ammonia release. The results reveal a common reaction pathway for LiNH2–LiH and LiNH2–LiH plus 1 mol% AlCl3 systems, but the thermodynamic properties are changed by the inclusion of Al3+ in the LiNH2 structure. These findings have important implications for tailoring the properties of the Li–N–H system.
Fil: Fernández Albanesi, Luisa Francisca. Comisión Nacional de Energía Atómica. Gerencia del Area de Energía Nuclear. Instituto Balseiro; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Arneodo Larochette, Pierre Paul. Comisión Nacional de Energía Atómica. Gerencia del Area de Energía Nuclear. Instituto Balseiro; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Gennari, Fabiana Cristina. Comisión Nacional de Energía Atómica. Gerencia del Area de Energía Nuclear. Instituto Balseiro; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina - Materia
-
Amide
Hydrogen Storage
Complex Hydride
Desorption - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/17575
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Destabilization of the LiNH2–LiH hydrogen storage system by aluminum incorporationFernández Albanesi, Luisa FranciscaArneodo Larochette, Pierre PaulGennari, Fabiana CristinaAmideHydrogen StorageComplex HydrideDesorptionhttps://purl.org/becyt/ford/2.5https://purl.org/becyt/ford/2The lithium amide–lithium hydride system (LiNH2–LiH) is one of the most attractive light-weight materials for hydrogen storage. In an effort to improve its hydrogen sorption kinetics, the effect of 1 mol% AlCl3 addition to LiNH2–LiH system was systematically investigated by differential scanning calorimetry, X-ray diffraction, Fourier transform infrared analysis and hydrogen volumetric measurements. It is shown that Al3+ is incorporated into the LiNH2 structure by partial substitution of Li+ forming a new amide in the Li–Al–N–H system, which is reversible under hydriding/dehydriding cycles. This new substituted amide displays improved hydrogen storage properties with respect to LiNH2–LiH. In fact, a stable hydrogen storage capacity of about 4.5–5.0 wt% is observed under cycling and is completely desorbed in 30 min at 275 °C for the Li–Al–N–H system. Moreover, the concurrent incorporation of Al3+ and the presence of LiH are effective for mitigating the ammonia release. The results reveal a common reaction pathway for LiNH2–LiH and LiNH2–LiH plus 1 mol% AlCl3 systems, but the thermodynamic properties are changed by the inclusion of Al3+ in the LiNH2 structure. These findings have important implications for tailoring the properties of the Li–N–H system.Fil: Fernández Albanesi, Luisa Francisca. Comisión Nacional de Energía Atómica. Gerencia del Area de Energía Nuclear. Instituto Balseiro; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Arneodo Larochette, Pierre Paul. Comisión Nacional de Energía Atómica. Gerencia del Area de Energía Nuclear. Instituto Balseiro; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Gennari, Fabiana Cristina. Comisión Nacional de Energía Atómica. Gerencia del Area de Energía Nuclear. Instituto Balseiro; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaElsevier2013-09info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/17575Fernández Albanesi, Luisa Francisca; Arneodo Larochette, Pierre Paul; Gennari, Fabiana Cristina; Destabilization of the LiNH2–LiH hydrogen storage system by aluminum incorporation; Elsevier; International Journal Of Hydrogen Energy; 38; 28; 9-2013; 12325-123340360-3199enginfo:eu-repo/semantics/altIdentifier/doi/10.1016/j.ijhydene.2013.07.030info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0360319913017308?via%3Dihubinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-10T13:24:21Zoai:ri.conicet.gov.ar:11336/17575instacron: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:34982025-09-10 13:24:21.858CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Destabilization of the LiNH2–LiH hydrogen storage system by aluminum incorporation |
title |
Destabilization of the LiNH2–LiH hydrogen storage system by aluminum incorporation |
spellingShingle |
Destabilization of the LiNH2–LiH hydrogen storage system by aluminum incorporation Fernández Albanesi, Luisa Francisca Amide Hydrogen Storage Complex Hydride Desorption |
title_short |
Destabilization of the LiNH2–LiH hydrogen storage system by aluminum incorporation |
title_full |
Destabilization of the LiNH2–LiH hydrogen storage system by aluminum incorporation |
title_fullStr |
Destabilization of the LiNH2–LiH hydrogen storage system by aluminum incorporation |
title_full_unstemmed |
Destabilization of the LiNH2–LiH hydrogen storage system by aluminum incorporation |
title_sort |
Destabilization of the LiNH2–LiH hydrogen storage system by aluminum incorporation |
dc.creator.none.fl_str_mv |
Fernández Albanesi, Luisa Francisca Arneodo Larochette, Pierre Paul Gennari, Fabiana Cristina |
author |
Fernández Albanesi, Luisa Francisca |
author_facet |
Fernández Albanesi, Luisa Francisca Arneodo Larochette, Pierre Paul Gennari, Fabiana Cristina |
author_role |
author |
author2 |
Arneodo Larochette, Pierre Paul Gennari, Fabiana Cristina |
author2_role |
author author |
dc.subject.none.fl_str_mv |
Amide Hydrogen Storage Complex Hydride Desorption |
topic |
Amide Hydrogen Storage Complex Hydride Desorption |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/2.5 https://purl.org/becyt/ford/2 |
dc.description.none.fl_txt_mv |
The lithium amide–lithium hydride system (LiNH2–LiH) is one of the most attractive light-weight materials for hydrogen storage. In an effort to improve its hydrogen sorption kinetics, the effect of 1 mol% AlCl3 addition to LiNH2–LiH system was systematically investigated by differential scanning calorimetry, X-ray diffraction, Fourier transform infrared analysis and hydrogen volumetric measurements. It is shown that Al3+ is incorporated into the LiNH2 structure by partial substitution of Li+ forming a new amide in the Li–Al–N–H system, which is reversible under hydriding/dehydriding cycles. This new substituted amide displays improved hydrogen storage properties with respect to LiNH2–LiH. In fact, a stable hydrogen storage capacity of about 4.5–5.0 wt% is observed under cycling and is completely desorbed in 30 min at 275 °C for the Li–Al–N–H system. Moreover, the concurrent incorporation of Al3+ and the presence of LiH are effective for mitigating the ammonia release. The results reveal a common reaction pathway for LiNH2–LiH and LiNH2–LiH plus 1 mol% AlCl3 systems, but the thermodynamic properties are changed by the inclusion of Al3+ in the LiNH2 structure. These findings have important implications for tailoring the properties of the Li–N–H system. Fil: Fernández Albanesi, Luisa Francisca. Comisión Nacional de Energía Atómica. Gerencia del Area de Energía Nuclear. Instituto Balseiro; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Arneodo Larochette, Pierre Paul. Comisión Nacional de Energía Atómica. Gerencia del Area de Energía Nuclear. Instituto Balseiro; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Gennari, Fabiana Cristina. Comisión Nacional de Energía Atómica. Gerencia del Area de Energía Nuclear. Instituto Balseiro; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina |
description |
The lithium amide–lithium hydride system (LiNH2–LiH) is one of the most attractive light-weight materials for hydrogen storage. In an effort to improve its hydrogen sorption kinetics, the effect of 1 mol% AlCl3 addition to LiNH2–LiH system was systematically investigated by differential scanning calorimetry, X-ray diffraction, Fourier transform infrared analysis and hydrogen volumetric measurements. It is shown that Al3+ is incorporated into the LiNH2 structure by partial substitution of Li+ forming a new amide in the Li–Al–N–H system, which is reversible under hydriding/dehydriding cycles. This new substituted amide displays improved hydrogen storage properties with respect to LiNH2–LiH. In fact, a stable hydrogen storage capacity of about 4.5–5.0 wt% is observed under cycling and is completely desorbed in 30 min at 275 °C for the Li–Al–N–H system. Moreover, the concurrent incorporation of Al3+ and the presence of LiH are effective for mitigating the ammonia release. The results reveal a common reaction pathway for LiNH2–LiH and LiNH2–LiH plus 1 mol% AlCl3 systems, but the thermodynamic properties are changed by the inclusion of Al3+ in the LiNH2 structure. These findings have important implications for tailoring the properties of the Li–N–H system. |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-09 |
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/11336/17575 Fernández Albanesi, Luisa Francisca; Arneodo Larochette, Pierre Paul; Gennari, Fabiana Cristina; Destabilization of the LiNH2–LiH hydrogen storage system by aluminum incorporation; Elsevier; International Journal Of Hydrogen Energy; 38; 28; 9-2013; 12325-12334 0360-3199 |
url |
http://hdl.handle.net/11336/17575 |
identifier_str_mv |
Fernández Albanesi, Luisa Francisca; Arneodo Larochette, Pierre Paul; Gennari, Fabiana Cristina; Destabilization of the LiNH2–LiH hydrogen storage system by aluminum incorporation; Elsevier; International Journal Of Hydrogen Energy; 38; 28; 9-2013; 12325-12334 0360-3199 |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ijhydene.2013.07.030 info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0360319913017308?via%3Dihub |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-nd/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier |
publisher.none.fl_str_mv |
Elsevier |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
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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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1842981350933528576 |
score |
12.48226 |