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Realization of a Half Metal with a Record-High Curie Temperature in Perovskite Oxides

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Wang,  Xiao
Physics of Correlated Matter, Max Planck Institute for Chemical Physics of Solids, Max Planck Society;

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Tjeng,  Liu Hao
Liu Hao Tjeng, Physics of Correlated Matter, Max Planck Institute for Chemical Physics of Solids, Max Planck Society;

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Hu,  Zhiwei
Zhiwei Hu, Physics of Correlated Matter, Max Planck Institute for Chemical Physics of Solids, Max Planck Society;

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Citation

Liu, Z., Zhang, S., Wang, X., Ye, X., Qin, S., Shen, X., et al. (2022). Realization of a Half Metal with a Record-High Curie Temperature in Perovskite Oxides. Advanced Materials, 34(17): 2200626, pp. 1-8. doi:10.1002/adma.202200626.


Cite as: https://hdl.handle.net/21.11116/0000-000A-6ED3-D
Abstract
Half metals, in which one spin channel is conducting while the other is insulating with an energy gap, are theoretically considered to comprise 100% spin-polarized conducting electrons, and thus have promising applications in high-efficiency magnetic sensors, computer memory, magnetic recording, and so on. However, for practical applications, a high Curie temperature combined with a wide spin energy gap and large magnetization is required. Realizing such a high-performance combination is a key challenge. Herein, a novel A- and B-site ordered quadruple perovskite oxide LaCu3Fe2Re2O12 with the charge format of Cu2+/Fe3+/Re4.5+ is reported. The strong Cu2+(up arrow)Fe3+(up arrow)Re4.5+(down arrow) spin interactions lead to a ferrimagnetic Curie temperature as high as 710 K, which is the reported record in perovskite-type half metals thus far. The saturated magnetic moment determined at 300 K is 7.0 mu(B) f.u.(-1) and further increases to 8.0 mu(B) f.u.(-1) at 2 K. First-principles calculations reveal a half-metallic nature with a spin-down conducting band while a spin-up insulating band with a large energy gap up to 2.27 eV. The currently unprecedented realization of record Curie temperature coupling with the wide energy gap and large moment in LaCu3Fe2Re2O12 opens a way for potential applications in advanced spintronic devices at/above room temperature.