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dc.contributor.author
Chaudhari, Hina N.  
dc.contributor.author
Pullar, Robert C.  
dc.contributor.author
Meena, Sher Singh  
dc.contributor.author
Singh, Charanjeet  
dc.contributor.author
Municoy, Sofia  
dc.contributor.author
Desimone, Martín Federico  
dc.contributor.author
Naqvi, Sayed Tathir Abbas  
dc.contributor.author
Jotania, Rajshree B.  
dc.date.available
2025-06-02T12:32:56Z  
dc.date.issued
2024-09  
dc.identifier.citation
Chaudhari, Hina N.; Pullar, Robert C.; Meena, Sher Singh; Singh, Charanjeet; Municoy, Sofia; et al.; Al 3+ substituted U-type hexaferrites Ba 4 Co 2 Fe 36− x Al x O 60 : structural, magnetic, electrical and dielectric properties; Royal Society of Chemistry; Journal of Materials Chemistry C; 12; 38; 9-2024; 15621-15643  
dc.identifier.issn
2050-7526  
dc.identifier.uri
http://hdl.handle.net/11336/263166  
dc.description.abstract
Polycrystalline samples of Al3+-substituted barium–cobalt U-type hexagonal ferrites, with the chemical composition Ba4Co2Fe36−xAlxO60 (x = 0.0, 0.2, 0.4, 0.6, 0.8 and 1.0), were synthesised using a citrate gel auto-combustion route and subsequently heated at 1300 °C for 5 h. To study the influence of Al3+ substitution on structural, magnetic, and dielectric characteristics, FTIR, XRD, SEM, EDX, M–H loops, Mössbauer spectroscopy and low frequency (up to 2 MHz) dielectric measurements were performed. Biocompatibility evaluation was also carried out with 3T3 fibroblast cells, and antioxidant capacity and antimicrobial activity were assessed. Agglomerated grains with different surface morphologies were seen in SEM images. EDX examination of all compositions showed the existence of Ba, Fe, Co and Al ions. Saturation magnetisation (MS) varied from 32.3 to 52.2 A m2 kg−1. A squareness ratio (Mr/MS) of < 0.5 was obtained, signifying that all the samples have multi-domain structures. However, all samples were magnetically soft ferrites, with HC kA m−1 found to vary from 62.1 Oe to 78.6 Oe (4.94 kA m−1 to 6.26 kA m−1). Mössbauer spectra were fitted with five sextets of five magnetic sublattices, and the results were obtained with a variation in Al content at room temperature. The composition x = 0.4 showed the highest value of relative area (12k site), whereas x = 1.0 showed the minimum value at the 12k site, indicating that Al3+ begins to replace Fe3+ in the 12k site. For compositions x = 0.2 and 0.4, Al3+ begins to replace Fe3+ in the 4f2 site, leading to an increase in the electron density in this site, but this electron density is reduced with further Al3+ substitution because as the number of Fe vacancies increases, Al3+ favours the 12k site. This results in a non-linear variation in magnetic properties with increasing aluminium substitution. Dielectric parameters such as dielectric constant, dielectric loss tangent, and AC conductivity were analysed as a function of frequency (10 Hz–2 MHz), and analysis results illustrate the typical behaviour of ferrimagnetic materials. The Cole–Cole type plot showed one semi-circle arc for all samples. Simulated impedance plots obtained through electrochemical impedance spectroscopy (EIS) software complied with the measured impedance of the samples and revealed a variation in simulated values of grain and grain boundary parameters, which was in agreement with SEM images. EIS generated simulated impedance plots that agreed with the measured impedance of the samples. The disclosed deviation in the simulated values of grain and grain boundary parameters was consistent with SEM micrographs. The grain morphology influenced the electrical parameters of ferrite samples, and dielectric relaxation was found to be prevalent in the samples.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Royal Society of Chemistry  
dc.rights
info:eu-repo/semantics/restrictedAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
hexaferrites  
dc.subject
Structural Properties  
dc.subject
Dielectric Properties.  
dc.subject
Magnetic and Electrical properties  
dc.subject.classification
Nano-materiales  
dc.subject.classification
Nanotecnología  
dc.subject.classification
INGENIERÍAS Y TECNOLOGÍAS  
dc.title
Al 3+ substituted U-type hexaferrites Ba 4 Co 2 Fe 36− x Al x O 60 : structural, magnetic, electrical and dielectric properties  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2025-05-30T13:53:01Z  
dc.identifier.eissn
2050-7534  
dc.journal.volume
12  
dc.journal.number
38  
dc.journal.pagination
15621-15643  
dc.journal.pais
Reino Unido  
dc.description.fil
Fil: Chaudhari, Hina N.. Gujarat University; India  
dc.description.fil
Fil: Pullar, Robert C.. Università Ca Foscari Venezia; Italia  
dc.description.fil
Fil: Meena, Sher Singh. Bhabha Atomic Research Centre; India  
dc.description.fil
Fil: Singh, Charanjeet. Lovely Professional University; India  
dc.description.fil
Fil: Municoy, Sofia. Universidad de Buenos Aires. Facultad de Farmacia y Bioquimica. Instituto de Química y Metabolismo del Fármaco; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Química y Metabolismo del Fármaco. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Instituto de Química y Metabolismo del Fármaco; Argentina  
dc.description.fil
Fil: Desimone, Martín Federico. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Química y Metabolismo del Fármaco. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Instituto de Química y Metabolismo del Fármaco; Argentina. Universidad de Buenos Aires. Facultad de Farmacia y Bioquimica. Instituto de Química y Metabolismo del Fármaco; Argentina  
dc.description.fil
Fil: Naqvi, Sayed Tathir Abbas. Lovely Professional University; India  
dc.description.fil
Fil: Jotania, Rajshree B.. Gujarat University, Ahmedabad; India  
dc.journal.title
Journal of Materials Chemistry C  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://xlink.rsc.org/?DOI=D4TC01659A  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1039/D4TC01659A