Strong exchange and magnetic blocking in N23--radical-bridged lanthanide complexes

被引:984
作者
Rinehart, Jeffrey D. [2 ]
Fang, Ming [1 ]
Evans, William J. [1 ]
Long, Jeffrey R. [2 ]
机构
[1] Univ Calif Irvine, Dept Chem, Irvine, CA 92697 USA
[2] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
基金
美国国家科学基金会;
关键词
SINGLE-MOLECULE MAGNET; ANISOTROPY BARRIER; RELAXATION; AGGREGATE; LEVEL; STATE;
D O I
10.1038/nchem.1063
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Single-molecule magnets approach the ultimate size limit for spin-based devices. These complexes can retain spin information over long periods of time at low temperature, suggesting possible applications in high-density information storage, quantum computing and spintronics. Notably, the success of most such applications hinges upon raising the inherent molecular spin-inversion barrier. Although recent advances have shown the viability of lanthanide-containing complexes in generating large barriers, weak or non-existent magnetic exchange coupling allows fast relaxation pathways that mitigate the full potential of these species. Here, we show that the diffuse spin of an N-2(3-) radical bridge can lead to exceptionally strong magnetic exchange in dinuclear Ln(II) (Ln = Gd, Dy) complexes. The Gd(III) congener exhibits the strongest magnetic coupling yet observed for that ion, while incorporation of the high-anisotropy Dy(III) ion gives rise to a molecule with a record magnetic blocking temperature of 8.3 K at a sweep rate of 0.08 T s(-1).
引用
收藏
页码:538 / 542
页数:5
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