Zeng, Xue, Liu, Jiaqian, Chu, Ke, He, Jie, Zhang, Junwei, Zhu, Hanxing ![]() ![]() |
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Abstract
Rare-earth doping has been proven to be an effective strategy for tailoring the magnetic properties of ferrites. In this study, we report a direct experimental observation of the precise occupation of cations in Ce-doped spinel ZnFe2O4 ferrites. We demonstrate that divalent Zn2+ cations and trivalent Fe3+ cations respectively occupy all tetrahedral A sites and all octahedral B sites in ZnFe2O4 nanofibers, which aligns well with the normal spinel structure. Rare-earth Ce3+ ions preferentially occupy the octahedral sites of the ZnFe2O4 lattice, while the excess Fe3+ ions are displaced to the tetrahedral sites. The observed behavior is possibly due to the greater bond energy of Ce3+–O2− relative to Fe3+–O2−, requiring additional energy for Ce3+ to substitute into the B-sites. This cation redistribution leading to the appearance of 4f–3d orbital couplings results in the changes in magnetic performance at room temperature. With increasing Ce3+ doping concentration, the saturation magnetization (Ms) first increases before reaching a maximum and subsequently decreases. ZnFe2O4 nanofibers doped with 0.05 mmol Ce3+ exhibit the highest Ms value due to the enhanced A–O–B super-exchange interaction.
Item Type: | Article |
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Date Type: | Published Online |
Status: | Published |
Schools: | Schools > Engineering |
Additional Information: | License information from Publisher: LICENSE 1: URL: https://creativecommons.org/licenses/by-nc/3.0/, Start Date: 2025-06-20 |
Publisher: | Royal Society of Chemistry |
Date of First Compliant Deposit: | 25 June 2025 |
Date of Acceptance: | 30 May 2025 |
Last Modified: | 25 Jun 2025 11:00 |
URI: | https://orca.cardiff.ac.uk/id/eprint/179320 |
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