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Nanocrystalline Antiferromagnetic High-κ Dielectric Sr(2)NiMO(6) (M = Te, W) with Double Perovskite Structure Type
Double perovskites have been extensively studied in materials chemistry due to their excellent properties and novel features attributed to the coexistence of ferro/ferri/antiferro-magnetic ground state and semiconductor band gap within the same material. Double perovskites with Sr(2)NiMO(6) (M = Te,...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7504737/ https://www.ncbi.nlm.nih.gov/pubmed/32887320 http://dx.doi.org/10.3390/molecules25173996 |
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author | Bijelić, Jelena Tatar, Dalibor Hajra, Sugato Sahu, Manisha Kim, Sang Jae Jagličić, Zvonko Djerdj, Igor |
author_facet | Bijelić, Jelena Tatar, Dalibor Hajra, Sugato Sahu, Manisha Kim, Sang Jae Jagličić, Zvonko Djerdj, Igor |
author_sort | Bijelić, Jelena |
collection | PubMed |
description | Double perovskites have been extensively studied in materials chemistry due to their excellent properties and novel features attributed to the coexistence of ferro/ferri/antiferro-magnetic ground state and semiconductor band gap within the same material. Double perovskites with Sr(2)NiMO(6) (M = Te, W) structure type have been synthesized using simple, non-toxic and costless aqueous citrate sol-gel route. The reaction yielded phase-pure nanocrystalline powders of two compounds: Sr(2)NiWO(6) (SNWO) and Sr(2)NiTeO(6) (SNTO). According to the Rietveld refinement of powder X-ray diffraction data at room temperature, Sr(2)NiWO(6) is tetragonal (I4/m) and Sr(2)NiTeO(6) is monoclinic (C12/m1), with average crystallite sizes of 49 and 77 nm, respectively. Structural studies have been additionally performed by Raman spectroscopy revealing optical phonons typical for vibrations of Te(6+)/W(6+)O(6) octahedra. Both SNTO and SNWO possess high values of dielectric constants (341 and 308, respectively) with low dielectric loss (0.06 for SNWO) at a frequency of 1 kHz. These values decrease exponentially with the increase of frequency to 1000 kHz, with the dielectric constant being around 260 for both compounds and dielectric loss being 0.01 for SNWO and 0.04 for SNTO. The Nyquist plot for both samples confirms the non-Debye type of relaxation behavior and the dominance of shorter-range movement of charge carriers. Magnetic studies of both compounds revealed antiferromagnetic behavior, with Néel temperature (T(N)) being 57 K for SNWO and 35 K for SNTO. |
format | Online Article Text |
id | pubmed-7504737 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-75047372020-09-26 Nanocrystalline Antiferromagnetic High-κ Dielectric Sr(2)NiMO(6) (M = Te, W) with Double Perovskite Structure Type Bijelić, Jelena Tatar, Dalibor Hajra, Sugato Sahu, Manisha Kim, Sang Jae Jagličić, Zvonko Djerdj, Igor Molecules Article Double perovskites have been extensively studied in materials chemistry due to their excellent properties and novel features attributed to the coexistence of ferro/ferri/antiferro-magnetic ground state and semiconductor band gap within the same material. Double perovskites with Sr(2)NiMO(6) (M = Te, W) structure type have been synthesized using simple, non-toxic and costless aqueous citrate sol-gel route. The reaction yielded phase-pure nanocrystalline powders of two compounds: Sr(2)NiWO(6) (SNWO) and Sr(2)NiTeO(6) (SNTO). According to the Rietveld refinement of powder X-ray diffraction data at room temperature, Sr(2)NiWO(6) is tetragonal (I4/m) and Sr(2)NiTeO(6) is monoclinic (C12/m1), with average crystallite sizes of 49 and 77 nm, respectively. Structural studies have been additionally performed by Raman spectroscopy revealing optical phonons typical for vibrations of Te(6+)/W(6+)O(6) octahedra. Both SNTO and SNWO possess high values of dielectric constants (341 and 308, respectively) with low dielectric loss (0.06 for SNWO) at a frequency of 1 kHz. These values decrease exponentially with the increase of frequency to 1000 kHz, with the dielectric constant being around 260 for both compounds and dielectric loss being 0.01 for SNWO and 0.04 for SNTO. The Nyquist plot for both samples confirms the non-Debye type of relaxation behavior and the dominance of shorter-range movement of charge carriers. Magnetic studies of both compounds revealed antiferromagnetic behavior, with Néel temperature (T(N)) being 57 K for SNWO and 35 K for SNTO. MDPI 2020-09-02 /pmc/articles/PMC7504737/ /pubmed/32887320 http://dx.doi.org/10.3390/molecules25173996 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Bijelić, Jelena Tatar, Dalibor Hajra, Sugato Sahu, Manisha Kim, Sang Jae Jagličić, Zvonko Djerdj, Igor Nanocrystalline Antiferromagnetic High-κ Dielectric Sr(2)NiMO(6) (M = Te, W) with Double Perovskite Structure Type |
title | Nanocrystalline Antiferromagnetic High-κ Dielectric Sr(2)NiMO(6) (M = Te, W) with Double Perovskite Structure Type |
title_full | Nanocrystalline Antiferromagnetic High-κ Dielectric Sr(2)NiMO(6) (M = Te, W) with Double Perovskite Structure Type |
title_fullStr | Nanocrystalline Antiferromagnetic High-κ Dielectric Sr(2)NiMO(6) (M = Te, W) with Double Perovskite Structure Type |
title_full_unstemmed | Nanocrystalline Antiferromagnetic High-κ Dielectric Sr(2)NiMO(6) (M = Te, W) with Double Perovskite Structure Type |
title_short | Nanocrystalline Antiferromagnetic High-κ Dielectric Sr(2)NiMO(6) (M = Te, W) with Double Perovskite Structure Type |
title_sort | nanocrystalline antiferromagnetic high-κ dielectric sr(2)nimo(6) (m = te, w) with double perovskite structure type |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7504737/ https://www.ncbi.nlm.nih.gov/pubmed/32887320 http://dx.doi.org/10.3390/molecules25173996 |
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