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Charge-Transfer-Based Mechanism for Half-Metallicity and Ferromagnetism in One-Dimensional Organometallic Sandwich Molecular Wires

机译:一维有机金属夹心分子线中半金属和铁磁性的基于电荷转移的机理

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摘要

We present a systematic theoretical study on the mechanism of half-metallicity and ferromagnetism for one-dimensional (1-D) sandwich molecular wires (SMWs) constructed with altering cyclopen-tadienyl (Cp) and first-row transition metal (Mt). It is unveiled for the first time that, in (MtCp)_∞, one valence electron would transfer from the Mt to the Cp ring, forming Cp~- and Mt~+ altering structures. This electron transfer not only makes them more stable than the benzene analogues (MtBz)_∞ but also leads to completely different half-metallic and ferromagnetic mechanisms. We analyze such unusual half-metallicity and ferromagnetic behaviors and explain each SMW magnetic moment quantitatively. Finally, we indicate that a Peierls transition does not occur in these 1-D SMWs.
机译:我们对半金属和铁磁性的机制进行系统的理论研究,以改变环pen-tadienyl(Cp)和第一行过渡金属(Mt)构成的一维(1-D)夹心分子线(SMWs)。首次揭示,在(MtCp)_∞中,一个价电子将从Mt转移到Cp环,形成Cp〜-和Mt〜+改变结构。这种电子转移不仅使它们比苯类似物(MtBz)_∞更稳定,而且导致了完全不同的半金属和铁磁机理。我们分析了这种异常的半金属性和铁磁行为,并定量地解释了每个SMW磁矩。最后,我们指出在这些1-D SMWs中不会发生Peierls过渡。

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