On the properties of NiO powders obtained by different wet chemical methods and calcination

Autores
Alastuey, Patricio; Pais Ospina, Daniel Humberto; Comedi, David Mario; Tirado, Monica Cecilia; Marín Ramírez, Oscar Alonso
Año de publicación
2023
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
NiO powders were synthesized using coprecipitation, sol-gel, and hydrothermal synthesis methods. The powders were subjected to calcination in atmospheric air, followed by recalcination in an O2-rich atmosphere at 800°C for 2 h each. Characterization techniques, such as scanning electron microscopy, X-ray diffraction, energy dispersive X-ray spectroscopy, and microRaman spectroscopy, were utilized. The coprecipitation and hydrothermal methods resulted in disaggregated submicrometric particles. The average size of particles obtained by the coprecipitation method after calcination in atmospheric air and recalcination in an O2-rich atmosphere was 360 ± 140 nm and 400 ± 130 nm, respectively. Regarding the particles obtained by the hydrothermal method, the average size was 190 ± 50 and 220 ± 80 nm for calcined in atmospheric air and recalcined in O2-rich atmosphere, respectively. Conversely, the sol-gel method produced particle aggregates with an average size of 430 ± 150 nm after calcination in atmospheric air and 500 ± 200 nm for calcination in an O2-rich atmosphere. X-ray diffraction analysis revealed that only the hydrothermal method yielded pure NiO without additional Ni-related phases, irrespective of the calcination procedure. In contrast, the coprecipitation sample exhibited a Ni2O3 phase after calcination in atmospheric air, which disappeared after recalcination in an O2-rich atmosphere. The sol-gel-derived sample maintained a Ni phase after both calcination processes. Analysis of the crystallite size demonstrated an increase after recalcination in an O2-rich atmosphere for the hydrothermal and sol-gel-derived samples, while a decrease was observed for the coprecipitation-derived sample. Raman spectra exhibited defect-enabled first-order forbidden phonon modes that were sensitive to the synthesis route. The two magnon phonon modes also demonstrated dependency on the route, indicating variations in defect structures. Photocatalytic evaluation using methylene blue degradation in aqueous solutions indicated better performance for the powders recalcined in an O2-rich atmosphere.
Fil: Alastuey, Patricio. Universidad Nacional de Tucumán. Instituto de Física del Noroeste Argentino. - Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet Noa Sur. Instituto de Física del Noroeste Argentino; Argentina
Fil: Pais Ospina, Daniel Humberto. Universidad Nacional de Tucumán. Instituto de Física del Noroeste Argentino. - Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet Noa Sur. Instituto de Física del Noroeste Argentino; Argentina
Fil: Comedi, David Mario. Universidad Nacional de Tucumán. Instituto de Física del Noroeste Argentino. - Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet Noa Sur. Instituto de Física del Noroeste Argentino; Argentina
Fil: Tirado, Monica Cecilia. Universidad Nacional de Tucumán. Instituto de Física del Noroeste Argentino. - Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet Noa Sur. Instituto de Física del Noroeste Argentino; Argentina
Fil: Marín Ramírez, Oscar Alonso. Universidad Nacional de Tucumán. Instituto de Física del Noroeste Argentino. - Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet Noa Sur. Instituto de Física del Noroeste Argentino; Argentina
Materia
NIO
PHOTOCATALYSIS
RAMAN SPECTROSCOPY
TWO MAGNON PHONON MODES
WET CHEMICAL SYNTHESIS
X-RAY DIFFRACTION
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/224116
Acceder
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oai_identifier_str oai:ri.conicet.gov.ar:11336/224116
network_acronym_str CONICETDig
repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling On the properties of NiO powders obtained by different wet chemical methods and calcinationAlastuey, PatricioPais Ospina, Daniel HumbertoComedi, David MarioTirado, Monica CeciliaMarín Ramírez, Oscar AlonsoNIOPHOTOCATALYSISRAMAN SPECTROSCOPYTWO MAGNON PHONON MODESWET CHEMICAL SYNTHESISX-RAY DIFFRACTIONhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1NiO powders were synthesized using coprecipitation, sol-gel, and hydrothermal synthesis methods. The powders were subjected to calcination in atmospheric air, followed by recalcination in an O2-rich atmosphere at 800°C for 2 h each. Characterization techniques, such as scanning electron microscopy, X-ray diffraction, energy dispersive X-ray spectroscopy, and microRaman spectroscopy, were utilized. The coprecipitation and hydrothermal methods resulted in disaggregated submicrometric particles. The average size of particles obtained by the coprecipitation method after calcination in atmospheric air and recalcination in an O2-rich atmosphere was 360 ± 140 nm and 400 ± 130 nm, respectively. Regarding the particles obtained by the hydrothermal method, the average size was 190 ± 50 and 220 ± 80 nm for calcined in atmospheric air and recalcined in O2-rich atmosphere, respectively. Conversely, the sol-gel method produced particle aggregates with an average size of 430 ± 150 nm after calcination in atmospheric air and 500 ± 200 nm for calcination in an O2-rich atmosphere. X-ray diffraction analysis revealed that only the hydrothermal method yielded pure NiO without additional Ni-related phases, irrespective of the calcination procedure. In contrast, the coprecipitation sample exhibited a Ni2O3 phase after calcination in atmospheric air, which disappeared after recalcination in an O2-rich atmosphere. The sol-gel-derived sample maintained a Ni phase after both calcination processes. Analysis of the crystallite size demonstrated an increase after recalcination in an O2-rich atmosphere for the hydrothermal and sol-gel-derived samples, while a decrease was observed for the coprecipitation-derived sample. Raman spectra exhibited defect-enabled first-order forbidden phonon modes that were sensitive to the synthesis route. The two magnon phonon modes also demonstrated dependency on the route, indicating variations in defect structures. Photocatalytic evaluation using methylene blue degradation in aqueous solutions indicated better performance for the powders recalcined in an O2-rich atmosphere.Fil: Alastuey, Patricio. Universidad Nacional de Tucumán. Instituto de Física del Noroeste Argentino. - Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet Noa Sur. Instituto de Física del Noroeste Argentino; ArgentinaFil: Pais Ospina, Daniel Humberto. Universidad Nacional de Tucumán. Instituto de Física del Noroeste Argentino. - Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet Noa Sur. Instituto de Física del Noroeste Argentino; ArgentinaFil: Comedi, David Mario. Universidad Nacional de Tucumán. Instituto de Física del Noroeste Argentino. - Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet Noa Sur. Instituto de Física del Noroeste Argentino; ArgentinaFil: Tirado, Monica Cecilia. Universidad Nacional de Tucumán. Instituto de Física del Noroeste Argentino. - Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet Noa Sur. Instituto de Física del Noroeste Argentino; ArgentinaFil: Marín Ramírez, Oscar Alonso. Universidad Nacional de Tucumán. Instituto de Física del Noroeste Argentino. - Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet Noa Sur. Instituto de Física del Noroeste Argentino; ArgentinaWiley Blackwell Publishing, Inc2023-09info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/224116Alastuey, Patricio; Pais Ospina, Daniel Humberto; Comedi, David Mario; Tirado, Monica Cecilia; Marín Ramírez, Oscar Alonso; On the properties of NiO powders obtained by different wet chemical methods and calcination; Wiley Blackwell Publishing, Inc; Journal of the American Ceramic Society; 107; 1; 9-2023; 92-1060002-7820CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://ceramics.onlinelibrary.wiley.com/doi/10.1111/jace.19433info:eu-repo/semantics/altIdentifier/doi/10.1111/jace.19433info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-22T11:07:20Zoai:ri.conicet.gov.ar:11336/224116instacron: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 11:07:20.713CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv On the properties of NiO powders obtained by different wet chemical methods and calcination
title On the properties of NiO powders obtained by different wet chemical methods and calcination
spellingShingle On the properties of NiO powders obtained by different wet chemical methods and calcination
Alastuey, Patricio
NIO
PHOTOCATALYSIS
RAMAN SPECTROSCOPY
TWO MAGNON PHONON MODES
WET CHEMICAL SYNTHESIS
X-RAY DIFFRACTION
title_short On the properties of NiO powders obtained by different wet chemical methods and calcination
title_full On the properties of NiO powders obtained by different wet chemical methods and calcination
title_fullStr On the properties of NiO powders obtained by different wet chemical methods and calcination
title_full_unstemmed On the properties of NiO powders obtained by different wet chemical methods and calcination
title_sort On the properties of NiO powders obtained by different wet chemical methods and calcination
dc.creator.none.fl_str_mv Alastuey, Patricio
Pais Ospina, Daniel Humberto
Comedi, David Mario
Tirado, Monica Cecilia
Marín Ramírez, Oscar Alonso
author Alastuey, Patricio
author_facet Alastuey, Patricio
Pais Ospina, Daniel Humberto
Comedi, David Mario
Tirado, Monica Cecilia
Marín Ramírez, Oscar Alonso
author_role author
author2 Pais Ospina, Daniel Humberto
Comedi, David Mario
Tirado, Monica Cecilia
Marín Ramírez, Oscar Alonso
author2_role author
author
author
author
dc.subject.none.fl_str_mv NIO
PHOTOCATALYSIS
RAMAN SPECTROSCOPY
TWO MAGNON PHONON MODES
WET CHEMICAL SYNTHESIS
X-RAY DIFFRACTION
topic NIO
PHOTOCATALYSIS
RAMAN SPECTROSCOPY
TWO MAGNON PHONON MODES
WET CHEMICAL SYNTHESIS
X-RAY DIFFRACTION
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv NiO powders were synthesized using coprecipitation, sol-gel, and hydrothermal synthesis methods. The powders were subjected to calcination in atmospheric air, followed by recalcination in an O2-rich atmosphere at 800°C for 2 h each. Characterization techniques, such as scanning electron microscopy, X-ray diffraction, energy dispersive X-ray spectroscopy, and microRaman spectroscopy, were utilized. The coprecipitation and hydrothermal methods resulted in disaggregated submicrometric particles. The average size of particles obtained by the coprecipitation method after calcination in atmospheric air and recalcination in an O2-rich atmosphere was 360 ± 140 nm and 400 ± 130 nm, respectively. Regarding the particles obtained by the hydrothermal method, the average size was 190 ± 50 and 220 ± 80 nm for calcined in atmospheric air and recalcined in O2-rich atmosphere, respectively. Conversely, the sol-gel method produced particle aggregates with an average size of 430 ± 150 nm after calcination in atmospheric air and 500 ± 200 nm for calcination in an O2-rich atmosphere. X-ray diffraction analysis revealed that only the hydrothermal method yielded pure NiO without additional Ni-related phases, irrespective of the calcination procedure. In contrast, the coprecipitation sample exhibited a Ni2O3 phase after calcination in atmospheric air, which disappeared after recalcination in an O2-rich atmosphere. The sol-gel-derived sample maintained a Ni phase after both calcination processes. Analysis of the crystallite size demonstrated an increase after recalcination in an O2-rich atmosphere for the hydrothermal and sol-gel-derived samples, while a decrease was observed for the coprecipitation-derived sample. Raman spectra exhibited defect-enabled first-order forbidden phonon modes that were sensitive to the synthesis route. The two magnon phonon modes also demonstrated dependency on the route, indicating variations in defect structures. Photocatalytic evaluation using methylene blue degradation in aqueous solutions indicated better performance for the powders recalcined in an O2-rich atmosphere.
Fil: Alastuey, Patricio. Universidad Nacional de Tucumán. Instituto de Física del Noroeste Argentino. - Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet Noa Sur. Instituto de Física del Noroeste Argentino; Argentina
Fil: Pais Ospina, Daniel Humberto. Universidad Nacional de Tucumán. Instituto de Física del Noroeste Argentino. - Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet Noa Sur. Instituto de Física del Noroeste Argentino; Argentina
Fil: Comedi, David Mario. Universidad Nacional de Tucumán. Instituto de Física del Noroeste Argentino. - Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet Noa Sur. Instituto de Física del Noroeste Argentino; Argentina
Fil: Tirado, Monica Cecilia. Universidad Nacional de Tucumán. Instituto de Física del Noroeste Argentino. - Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet Noa Sur. Instituto de Física del Noroeste Argentino; Argentina
Fil: Marín Ramírez, Oscar Alonso. Universidad Nacional de Tucumán. Instituto de Física del Noroeste Argentino. - Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet Noa Sur. Instituto de Física del Noroeste Argentino; Argentina
description NiO powders were synthesized using coprecipitation, sol-gel, and hydrothermal synthesis methods. The powders were subjected to calcination in atmospheric air, followed by recalcination in an O2-rich atmosphere at 800°C for 2 h each. Characterization techniques, such as scanning electron microscopy, X-ray diffraction, energy dispersive X-ray spectroscopy, and microRaman spectroscopy, were utilized. The coprecipitation and hydrothermal methods resulted in disaggregated submicrometric particles. The average size of particles obtained by the coprecipitation method after calcination in atmospheric air and recalcination in an O2-rich atmosphere was 360 ± 140 nm and 400 ± 130 nm, respectively. Regarding the particles obtained by the hydrothermal method, the average size was 190 ± 50 and 220 ± 80 nm for calcined in atmospheric air and recalcined in O2-rich atmosphere, respectively. Conversely, the sol-gel method produced particle aggregates with an average size of 430 ± 150 nm after calcination in atmospheric air and 500 ± 200 nm for calcination in an O2-rich atmosphere. X-ray diffraction analysis revealed that only the hydrothermal method yielded pure NiO without additional Ni-related phases, irrespective of the calcination procedure. In contrast, the coprecipitation sample exhibited a Ni2O3 phase after calcination in atmospheric air, which disappeared after recalcination in an O2-rich atmosphere. The sol-gel-derived sample maintained a Ni phase after both calcination processes. Analysis of the crystallite size demonstrated an increase after recalcination in an O2-rich atmosphere for the hydrothermal and sol-gel-derived samples, while a decrease was observed for the coprecipitation-derived sample. Raman spectra exhibited defect-enabled first-order forbidden phonon modes that were sensitive to the synthesis route. The two magnon phonon modes also demonstrated dependency on the route, indicating variations in defect structures. Photocatalytic evaluation using methylene blue degradation in aqueous solutions indicated better performance for the powders recalcined in an O2-rich atmosphere.
publishDate 2023
dc.date.none.fl_str_mv 2023-09
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/11336/224116
Alastuey, Patricio; Pais Ospina, Daniel Humberto; Comedi, David Mario; Tirado, Monica Cecilia; Marín Ramírez, Oscar Alonso; On the properties of NiO powders obtained by different wet chemical methods and calcination; Wiley Blackwell Publishing, Inc; Journal of the American Ceramic Society; 107; 1; 9-2023; 92-106
0002-7820
CONICET Digital
CONICET
url http://hdl.handle.net/11336/224116
identifier_str_mv Alastuey, Patricio; Pais Ospina, Daniel Humberto; Comedi, David Mario; Tirado, Monica Cecilia; Marín Ramírez, Oscar Alonso; On the properties of NiO powders obtained by different wet chemical methods and calcination; Wiley Blackwell Publishing, Inc; Journal of the American Ceramic Society; 107; 1; 9-2023; 92-106
0002-7820
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://ceramics.onlinelibrary.wiley.com/doi/10.1111/jace.19433
info:eu-repo/semantics/altIdentifier/doi/10.1111/jace.19433
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Wiley Blackwell Publishing, Inc
publisher.none.fl_str_mv Wiley Blackwell Publishing, Inc
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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score 12.982451

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