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Influence of La3+ ions on the structural, optical and dielectric properties and ligand field parameters of Fe3+ hybrid borate glasses
•Entry of La3+ ions as a network modifier led to further structural modifications.•Optical spectra of Fe3+ ions in the visible region can be tuned by La3+ addition.•ESR spectra and Nephelauxetic effect confirmed the covalent nature of Fe3+ ions.•Dielectric constant and dielectric loss coefficient de...
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Published in: | Journal of non-crystalline solids 2023-01, Vol.599, p.121981, Article 121981 |
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container_start_page | 121981 |
container_title | Journal of non-crystalline solids |
container_volume | 599 |
creator | Abul-Magd, Ashraf A. Abu-Khadra, Ahmad S. Taha, Ashraf M. Basry, A.A.H. |
description | •Entry of La3+ ions as a network modifier led to further structural modifications.•Optical spectra of Fe3+ ions in the visible region can be tuned by La3+ addition.•ESR spectra and Nephelauxetic effect confirmed the covalent nature of Fe3+ ions.•Dielectric constant and dielectric loss coefficient decreased by La2O3 addition.•Fe3+ ions occupied tetrahedral/octahedral sites as confirmed by UV & ESR spectra.
The effect of TM/RE mixture (i.e., Fe3+/La3+) on the optical, structural and dielectric features of alkali borate glass was investigated. XRD spectra showed the successful formation of the glass matrix. The La2O3 doping as a network modifier imposed some structural modifications, such as a ∼20% growth in density, ∼15% reduction in molar volume, and an increase in the proportion of BO4 units with a decrease in NBO's ratio. The optical spectra associated with Fe3+ ions occupying the tetrahedral and octahedral sites were subjected to tunability within the visible range by La2O3 additions. Many optical and dielectric features are greatly enhanced; Such as bandgap energy, Urbach energy, linear/nonlinear refractive index, dielectric constant and dielectric loss. The metallization criterion decreased from 0.368 to 0.364 eV−1, reflecting the semiconductor nature of the samples. The nephelauxetic effect confirmed the covalent bonding nature of Fe3+ ions, consistent with the results of ESR spectra. |
doi_str_mv | 10.1016/j.jnoncrysol.2022.121981 |
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The effect of TM/RE mixture (i.e., Fe3+/La3+) on the optical, structural and dielectric features of alkali borate glass was investigated. XRD spectra showed the successful formation of the glass matrix. The La2O3 doping as a network modifier imposed some structural modifications, such as a ∼20% growth in density, ∼15% reduction in molar volume, and an increase in the proportion of BO4 units with a decrease in NBO's ratio. The optical spectra associated with Fe3+ ions occupying the tetrahedral and octahedral sites were subjected to tunability within the visible range by La2O3 additions. Many optical and dielectric features are greatly enhanced; Such as bandgap energy, Urbach energy, linear/nonlinear refractive index, dielectric constant and dielectric loss. The metallization criterion decreased from 0.368 to 0.364 eV−1, reflecting the semiconductor nature of the samples. The nephelauxetic effect confirmed the covalent bonding nature of Fe3+ ions, consistent with the results of ESR spectra.</description><identifier>ISSN: 0022-3093</identifier><identifier>EISSN: 1873-4812</identifier><identifier>DOI: 10.1016/j.jnoncrysol.2022.121981</identifier><language>eng</language><publisher>Elsevier B.V</publisher><ispartof>Journal of non-crystalline solids, 2023-01, Vol.599, p.121981, Article 121981</ispartof><rights>2022 Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c248t-88f2c625fd7448954a2666d989b47e08e482bebac57d32e8868b98af662f5cf93</citedby><cites>FETCH-LOGICAL-c248t-88f2c625fd7448954a2666d989b47e08e482bebac57d32e8868b98af662f5cf93</cites><orcidid>0000-0003-0222-1520</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Abul-Magd, Ashraf A.</creatorcontrib><creatorcontrib>Abu-Khadra, Ahmad S.</creatorcontrib><creatorcontrib>Taha, Ashraf M.</creatorcontrib><creatorcontrib>Basry, A.A.H.</creatorcontrib><title>Influence of La3+ ions on the structural, optical and dielectric properties and ligand field parameters of Fe3+ hybrid borate glasses</title><title>Journal of non-crystalline solids</title><description>•Entry of La3+ ions as a network modifier led to further structural modifications.•Optical spectra of Fe3+ ions in the visible region can be tuned by La3+ addition.•ESR spectra and Nephelauxetic effect confirmed the covalent nature of Fe3+ ions.•Dielectric constant and dielectric loss coefficient decreased by La2O3 addition.•Fe3+ ions occupied tetrahedral/octahedral sites as confirmed by UV & ESR spectra.
The effect of TM/RE mixture (i.e., Fe3+/La3+) on the optical, structural and dielectric features of alkali borate glass was investigated. XRD spectra showed the successful formation of the glass matrix. The La2O3 doping as a network modifier imposed some structural modifications, such as a ∼20% growth in density, ∼15% reduction in molar volume, and an increase in the proportion of BO4 units with a decrease in NBO's ratio. The optical spectra associated with Fe3+ ions occupying the tetrahedral and octahedral sites were subjected to tunability within the visible range by La2O3 additions. Many optical and dielectric features are greatly enhanced; Such as bandgap energy, Urbach energy, linear/nonlinear refractive index, dielectric constant and dielectric loss. The metallization criterion decreased from 0.368 to 0.364 eV−1, reflecting the semiconductor nature of the samples. The nephelauxetic effect confirmed the covalent bonding nature of Fe3+ ions, consistent with the results of ESR spectra.</description><issn>0022-3093</issn><issn>1873-4812</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNqFkMtOwzAQRS0EEqXwD95DQuwkjrOEikelSmxgbTn2uHXkxpHtIvUD-G8SisSS2dzFzD0aHYQwKXJSEHbf5_3gBxWO0bucFpTmhJKWkzO0ILwps4oTeo4WxbTJyqItL9FVjH0xTVPyBfpaD8YdYFCAvcEbWd5i64eI_YDTDnBM4aDSIUh3h_2YrJIOy0FjbcGBSsEqPAY_QkgW4s_G2e0cZjrQeJRB7iFBiDP9GSb67tgFq3Hng0yAt07GCPEaXRjpItz85hJ9PD-9r16zzdvLevWwyRSteMo4N1QxWhvdVBVv60pSxphuedtVDRQcKk476KSqG11S4JzxruXSMEZNrUxbLhE_cVXwMQYwYgx2L8NRkELMOkUv_nSKWac46Zyqj6cqTP99WggiKjt70zZMJoT29n_IN2kAhaU</recordid><startdate>20230101</startdate><enddate>20230101</enddate><creator>Abul-Magd, Ashraf A.</creator><creator>Abu-Khadra, Ahmad S.</creator><creator>Taha, Ashraf M.</creator><creator>Basry, A.A.H.</creator><general>Elsevier B.V</general><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0003-0222-1520</orcidid></search><sort><creationdate>20230101</creationdate><title>Influence of La3+ ions on the structural, optical and dielectric properties and ligand field parameters of Fe3+ hybrid borate glasses</title><author>Abul-Magd, Ashraf A. ; Abu-Khadra, Ahmad S. ; Taha, Ashraf M. ; Basry, A.A.H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c248t-88f2c625fd7448954a2666d989b47e08e482bebac57d32e8868b98af662f5cf93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Abul-Magd, Ashraf A.</creatorcontrib><creatorcontrib>Abu-Khadra, Ahmad S.</creatorcontrib><creatorcontrib>Taha, Ashraf M.</creatorcontrib><creatorcontrib>Basry, A.A.H.</creatorcontrib><collection>CrossRef</collection><jtitle>Journal of non-crystalline solids</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Abul-Magd, Ashraf A.</au><au>Abu-Khadra, Ahmad S.</au><au>Taha, Ashraf M.</au><au>Basry, A.A.H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Influence of La3+ ions on the structural, optical and dielectric properties and ligand field parameters of Fe3+ hybrid borate glasses</atitle><jtitle>Journal of non-crystalline solids</jtitle><date>2023-01-01</date><risdate>2023</risdate><volume>599</volume><spage>121981</spage><pages>121981-</pages><artnum>121981</artnum><issn>0022-3093</issn><eissn>1873-4812</eissn><abstract>•Entry of La3+ ions as a network modifier led to further structural modifications.•Optical spectra of Fe3+ ions in the visible region can be tuned by La3+ addition.•ESR spectra and Nephelauxetic effect confirmed the covalent nature of Fe3+ ions.•Dielectric constant and dielectric loss coefficient decreased by La2O3 addition.•Fe3+ ions occupied tetrahedral/octahedral sites as confirmed by UV & ESR spectra.
The effect of TM/RE mixture (i.e., Fe3+/La3+) on the optical, structural and dielectric features of alkali borate glass was investigated. XRD spectra showed the successful formation of the glass matrix. The La2O3 doping as a network modifier imposed some structural modifications, such as a ∼20% growth in density, ∼15% reduction in molar volume, and an increase in the proportion of BO4 units with a decrease in NBO's ratio. The optical spectra associated with Fe3+ ions occupying the tetrahedral and octahedral sites were subjected to tunability within the visible range by La2O3 additions. Many optical and dielectric features are greatly enhanced; Such as bandgap energy, Urbach energy, linear/nonlinear refractive index, dielectric constant and dielectric loss. The metallization criterion decreased from 0.368 to 0.364 eV−1, reflecting the semiconductor nature of the samples. The nephelauxetic effect confirmed the covalent bonding nature of Fe3+ ions, consistent with the results of ESR spectra.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.jnoncrysol.2022.121981</doi><orcidid>https://orcid.org/0000-0003-0222-1520</orcidid></addata></record> |
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title | Influence of La3+ ions on the structural, optical and dielectric properties and ligand field parameters of Fe3+ hybrid borate glasses |
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