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嵌入表面分子网络中的单个原子自旋的大磁各向异性。

Large magnetic anisotropy of a single atomic spin embedded in a surface molecular network.

作者信息

Hirjibehedin Cyrus F, Lin Chiung-Yuan, Otte Alexander F, Ternes Markus, Lutz Christopher P, Jones Barbara A, Heinrich Andreas J

机构信息

IBM Research Division, Almaden Research Center, San Jose, CA 95120, USA.

出版信息

Science. 2007 Aug 31;317(5842):1199-203. doi: 10.1126/science.1146110.

Abstract

Magnetic anisotropy allows magnets to maintain their direction of magnetization over time. Using a scanning tunneling microscope to observe spin excitations, we determined the orientation and strength of the anisotropies of individual iron and manganese atoms on a thin layer of copper nitride. The relative intensities of the inelastic tunneling processes are consistent with dipolar interactions, as seen for inelastic neutron scattering. First-principles calculations indicate that the magnetic atoms become incorporated into a polar covalent surface molecular network in the copper nitride. These structures, which provide atom-by-atom accessibility via local probes, have the potential for engineering anisotropies large enough to produce stable magnetization at low temperatures for a single atomic spin.

摘要

磁各向异性使磁体能够随时间保持其磁化方向。我们使用扫描隧道显微镜来观察自旋激发,确定了氮化铜薄层上单个铁原子和锰原子的各向异性的取向和强度。非弹性隧穿过程的相对强度与非弹性中子散射中观察到的偶极相互作用一致。第一性原理计算表明,磁性原子融入了氮化铜中的极性共价表面分子网络。这些结构通过局部探针提供逐个原子的可及性,有可能设计出足够大的各向异性,以便在低温下为单个原子自旋产生稳定的磁化。

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