首页> 外文期刊>Journal of Physics. Condensed Matter >Realizing stable half-metallicity in zigzag silicene nanoribbons with edge dihydrogenation and chemical doping
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Realizing stable half-metallicity in zigzag silicene nanoribbons with edge dihydrogenation and chemical doping

机译:用边缘二氢化和化学掺杂实现Zigzag硅纳米波动中稳定的半金属性

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摘要

Although many schemes have been proposed to obtain full half-metallicity in zigzag silicene nanoribbons with edge monohydrogenation (H-H ZSiNRs) by chemical modification, the resulted negligible energy difference between the antiferromagnetic (AFM) and ferromagnetic (FM) configurations makes the half-metallicity hardly observable practically. In this work, based on density functional calculations, we find that the ZSiNRs with edge dihydrogenation (H2-H2 ZSiNRs) can be tuned to be half-metallic by replacing the central two zigzag Si chains with two zigzag Al-P chains, and more importantly, the FM-AFM energy difference is significantly increased compared with the H-H cases. The obtained half-metallicity originates from the different potential between two edges of the ribbon after doping, which results in the edge states of two spin channels shifting oppositely in energy. This mechanism is so robust that the half-metallicity can always be achieved, irrespective of the ribbon width. Our finding provides a fantastic way for achieving stable half-metallicity in ZSiNRs.
机译:虽然已经提出了许多方案,通过化学改性获得具有边缘单加氢(H-H ZSiNRs)的锯齿形硅纳米带的完全半金属性,但由此产生的反铁磁(AFM)和铁磁(FM)构型之间的可忽略的能量差使得半金属性在实际中很难观察到。在这项工作中,基于密度泛函计算,我们发现,通过用两条锯齿形Al-P链替换中心两条锯齿形Si链,带边缘二氢化的ZSINR(H2-H2 ZSINR)可以被调谐为半金属,更重要的是,与H-H情况相比,FM-AFM能量差显著增加。所获得的半金属丰度源于掺杂后薄带两个边缘之间的不同电势,这导致两个自旋通道的边缘态在能量上发生相反的移动。这种机制是如此强大,以至于无论色带宽度如何,始终可以实现半金属丰度。我们的发现为在ZSINR中获得稳定的半金属丰度提供了一种极好的方法。

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