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Building high-performance magnetic materials out of gas-phase nanoclusters

机译:利用气相纳米团簇构建高性能磁性材料

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It is well known that free magnetic nanoclusters display novel properties including enhanced magnetic moments in ferromagnetic metals, ferrimagnetism in antiferromagnetic metals and the appearance of magnetism in non-magnetic metals. A contemporary challenge is to build some of the intrinsic novel behaviour into macroscopic materials. XMCD measurements of exposed mass-selected Fe clusters in the size range 180-700 atoms deposited in situ onto HOPG substrates reveal that adsorbed clusters show an enhancement in both orbital and spin moments relative to the bulk. Coating the exposed Fe clusters with Co increases the spin moment still further without significantly changing the orbital moment. Increasing the surface density of Fe clusters to induce a significant interaction reduces the orbital moment to its small bulk value but an enhancement in the spin moment remains even in thick cluster-assembled films. The anisotropy in isolated Fe and Co clusters embedded in Ag matrices is shown to be uniaxial with the anisotropy axes randomly oriented in three dimensions. Thick cluster films adopt a domainless correlated super-spin glass magnetic configuration as a result of the frustration between the inter-cluster exchange coupling and random anisotropy. This state is magnetically soft, which is a valuable technological attribute in high-moment films.
机译:众所周知,自由磁性纳米团簇显示出新颖的特性,包括铁磁金属中增强的磁矩,反铁磁金属中的亚铁磁性以及非磁性金属中的磁性外观。当代的挑战是将某些固有的新颖行为纳入宏观材料。 XMCD测量结果显示,在原位沉积在HOPG衬底上的,质量范围为180-700个原子的暴露的质量选择的Fe团簇显示,相对于团簇,吸附的团簇在轨道矩和自旋矩上都有增强。用Co覆盖暴露的Fe团簇会进一步增加自旋矩,而不会明显改变轨道矩。增加Fe团簇的表面密度以引起明显的相互作用,可将轨道矩减小到其较小的体积值,但即使在厚的团簇组装膜中,自旋矩仍保持增强。嵌入银基体中的孤立的Fe和Co团簇中的各向异性被证明是单轴的,各向异性轴随机地定向在三个维度上。由于簇间交换耦合和随机各向异性之间的挫败,厚的簇状膜采用了无畴相关的超旋转玻璃磁结构。这种状态在磁性上是软的,这在高力矩薄膜中是有价值的技术属性。

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