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arXiv 1608.03372cond-mat.str-el
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利用化学无序对磁螺旋进行室温以上调谐

Tuning magnetic spirals beyond room temperature with chemical disorder

Mickaël Morin, Emmanuel Canévet, Adrien Raynaud, Marek Bartkowiak, Denis Sheptyakov, Voraksmy Ban, Michel Kenzelmann, Ekaterina Pomjakushina, Kazimierz Conder, Marisa Medarde

摘要:

在过去的几年里,磁驱动铁电性和巨大的磁电效应已被报道的一些挫折磁铁与螺旋磁秩序。这种材料由于其用于自旋电子学和低功率磁电器件的潜力而具有高电流兴趣。然而,它们的低磁序温度(通常<100 K)极大地限制了它们的应用领域。在这里,我们表明,在钙钛矿YBaCuFeO 5的螺旋相的稳定域可以扩大超过150 K,通过控制操作的Fe/Cu化学无序。此外,我们还证明了这种新的机制可以在零磁场下将YBaCuFeO 5的磁螺旋态稳定在25°C以上。我们的研究结果表明,磁螺旋的性质,包括其波长和稳定范围,可以通过控制化学无序来设计,为设计具有室温以上磁电性能的材料提供了巨大的潜力。

英文摘要:

In the past years, magnetism-driven ferroelectricity and gigantic magnetoelectric effects have been reported for a number of frustrated magnets with spiral magnetic orders. Such materials are of high current interest due to their potential for spintronics and low-power magnetoelectric devices. However, their low magnetic order temperatures (typically <100K) greatly restrict their fields of application. Here we demonstrate that the stability domain of the spiral phase in the perovskite YBaCuFeO5 can be enlarged by more than 150K through a controlled manipulation of the Fe/Cu chemical disorder. Moreover we show that this novel mechanism can stabilize the magnetic spiral state of YBaCuFeO5 above the symbolic value of 25°C at zero magnetic field. Our findings demonstrate that the properties of a magnetic spiral, including its wavelength and stability range, can be engineered through the control of chemical disorder, offering a great potential for the design of materials with magnetoelectric properties beyond room temperature.

机构、总结、中文摘要均由AI分析而来,可能存在错误,请以论文正文为准。

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