2D Ruddlesden‐Popper Phase Hydride Double Perovskite A4NiVH8 (A = Na, K, Rb): Ferromagnetic Semiconductors With High Curie Temperatures

超级交换 居里温度 铁磁性 凝聚态物理 自旋电子学 离子半径 磁性半导体 材料科学 钙钛矿(结构) 氢化物 化学 结晶学 离子 物理 有机化学 冶金 金属
作者
Chao Jia,Xingxing Li,Qunxiang Li
出处
期刊:Small methods [Wiley]
标识
DOI:10.1002/smtd.202501380
摘要

Abstract 2D ferromagnetic semiconductors are recognized as the cornerstone of next‐generation spintronics devices. However, their practical applications are severely hindered by the low Curie temperature, which originates from the weak d‐p‐d ferromagnetic superexchange interaction. H − anion with short ionic radius can effectively shorten the distance between magnetic centers and simultaneously induce a perfect 180° superexchange angle to strengthen the magnetic coupling, thus achieving high‐temperature magnetic ordering. Here, by first‐principles calculations, such a case in 2D Ruddlesden‐Popper phase hydride double perovskite A 4 NiVH 8 (A = Na, K, Rb) is demonstrated. These hydride monolayers possess quite good thermodynamic stability and can retain their structures under normal pressure at least at 500 K. Magnetic and electronic properties calculations reveal that they are all ferromagnetic semiconductors with high Curie temperatures (up to 429 K) and superior electron mobilities (up to 5522 cm 2 V −1 s −1 , based on the deformation potential theory). In addition, monolayer Na 4 NiVH 8 exhibits the characteristics of a bipolar magnetic semiconductor with gate‐tunable spin polarization.
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