Presentation Information
[8p-E217-4]Tuning of Fe4O15 cluster magnetism by chemical substitution for Ba6La2Fe4O15
〇(D)Takumi Shirasaki1, Taro Matsuzawa1, Taichi Ishikawa1, Hideki Kuwahara1 (1.Sophia Univ.)
Keywords:
cluster magnetism,multiferroics,3d transition metal
Polar magnets with broken inversion symmetry in the paramagnetic phase are promising hosts for large magnetoelectric effects. Ba6La2Fe4O15 is the new polar magnet contain Fe4O15 clusters. Intra-cluster superexchange interactions bind the four Fe3+ (S = 5/2) spins into a total spin ST = 5, giving a cluster-paramagnetic state that hosts a magnetoelectric effect. To clarify how the electronic state governs this cluster magnetism, we synthesized the solid solution Ba6La2(Fe1-xCox)4O15. The Fe end member orders antiferromagnetically at TN = 12.8 K, whereas the Co end member shows a spin-glass transition at TSG = 62 K. This indicates a low-spin Co3+ that quenches the intra-cluster superexchange interactions, leading to the collapse of the total spin. Cluster magnetism is thus tunable via electronic configuration and site occupancy of the substituent ions.
