...
首页> 外文期刊>Chemical Physics: A Journal Devoted to Experimental and Theoretical Research Involving Problems of Both a Chemical and Physical Nature >Anisotropic double exchange in a valence-delocalized [Fe2.5+Fe2.5+] cluster. Spin-orbit coupling in the Anderson-Hasegawa double exchange model
【24h】

Anisotropic double exchange in a valence-delocalized [Fe2.5+Fe2.5+] cluster. Spin-orbit coupling in the Anderson-Hasegawa double exchange model

机译:价离域[Fe2.5 + Fe2.5 +]簇中的各向异性双交换。安德森-长谷川双交换模型中的自旋轨道耦合

获取原文
获取原文并翻译 | 示例

摘要

Anisotropic double exchange interaction is considered for the valence-delocalized [Fe2.5+Fe2.5+] cluster with strong Anderson-Hasegawa double exchange (DE) coupling. The combined effect of spin-orbit interaction and DE between the excited states of the mixed-valence Fe ions results in the inter-ion anisotropic DE coupling. The coefficients of anisotropic DE coupling are linearly proportional to the parameters B-o and B-mu of the DE interaction in the ground and excited cluster states. The anisotropic DE interaction operates between the cluster states of different localizations of the extra electron. The anisotropic DE coupling results in the zero-field splitting (ZFS) of the valence-delocalized ground state of the [Fe2.5+Fe2.5+] cluster. The ZFS of the anisotropic DE origin is specific for the delocalized mixed-valence systems and is described by the new effective ZFS Hamiltonian H'(ZFS). The ZFS Hamiltonian H'(ZFS) includes the operator of the Anderson-Hasegawa DE interaction and is active between the cluster states of different localizations, whereas the standard ZFS Hamiltonian, H-ZFS(o), acts in the localized states. The contributions of the anisotropic DE origin to the cluster ZFS parameters are linearly proportional to the DE parameters B-o, B-mu and depend on the total spin S. The anisotropic DE contribution to the cluster ZFS parameter of the ground valence-delocalized state is of the same order of magnitude as the single-ion ZFS contributions. (C) 2006 Elsevier B.V. All rights reserved.
机译:具有强安德森-长谷川双交换(DE)耦合的价离域[Fe2.5 + Fe2.5 +]团簇被认为是各向异性的双交换相互作用。混合价Fe离子的激发态之间的自旋轨道相互作用和DE的组合效应导致离子间各向异性DE耦合。各向异性DE耦合的系数与基态和激发簇态中DE相互作用的参数B-o和B-mu成线性比例。各向异性DE相互作用在额外电子的不同局部的团簇状态之间起作用。各向异性的DE耦合导致[Fe2.5 + Fe2.5 +]团簇的价离域基态的零场分裂(ZFS)。各向异性DE起源的ZFS特定于离域混合价系统,并由新的有效ZFS哈密顿量H'(ZFS)描述。 ZFS哈密顿量H'(ZFS)包括Anderson-Hasegawa DE相互作用的算子,并且在不同位置的簇状态之间处于活动状态,而标准ZFS哈密顿量H-ZFS(o)在局部状态下起作用。各向异性DE原点对簇ZFS参数的贡献与DE参数Bo,B-mu成线性比例,并且取决于总自旋S。各向异性DE对地价离域态簇ZFS参数的贡献为与单离子ZFS贡献量级相同。 (C)2006 Elsevier B.V.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号