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arXiv 1201.5864cond-mat.str-el
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分子基磁体的磁性能选择

Dimensionality selection in a molecule-based magnet

Paul A. Goddard, Jamie L. Manson, John Singleton, Isabel Franke, Tom Lancaster, Andrew J. Steele, Stephen J. Blundell, Christopher Baines, Francis L. Pratt, Ros… 展开作者

Paul A. Goddard, Jamie L. Manson, John Singleton, Isabel Franke, Tom Lancaster, Andrew J. Steele, Stephen J. Blundell, Christopher Baines, Francis L. Pratt, Ross D. McDonald, Oscar E. Ayala-Valenzuela, Jordan F. Corbey, Heather I. Southerland, Pinaki Sengupta, John A. Schlueter

摘要:

获得对磁性材料构建块的控制并从而实现特定特性将使定制磁性设备的设计和生长成为可能。虽然分子材料,特别是配位聚合物的合成进展代表了朝着这一目标迈出的重要一步,但在特定框架内调节磁相互作用的能力仍处于起步阶段。在这里,我们展示了一种化学方法,通过优先抑制磁交换在$S=1/2$反铁磁体沿一个晶体方向,切换系统的准二维到准一维,同时有效地保持最近邻耦合强度的维度选择。

英文摘要:

Gaining control of the building blocks of magnetic materials and thereby achieving particular characteristics will make possible the design and growth of bespoke magnetic devices. While progress in the synthesis of molecular materials, and especially coordination polymers, represents a significant step towards this goal, the ability to tune the magnetic interactions within a particular framework remains in its infancy. Here we demonstrate a chemical method which achieves dimensionality selection via preferential inhibition of the magnetic exchange in an $S=1/2$ antiferromagnet along one crystal direction, switching the system from being quasi-two- to quasi-one-dimensional while effectively maintaining the nearest-neighbour coupling strength.

机构、总结、中文摘要均由AI分析而来,可能存在错误,请以论文正文为准。

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