Reaching the magnetic anisotropy limit of a 3d metal atom

被引:309
|
作者
Rau, Ileana G. [1 ]
Baumann, Susanne [1 ,2 ]
Rusponi, Stefano [3 ]
Donati, Fabio [3 ]
Stepanow, Sebastian [4 ]
Gragnaniello, Luca [3 ]
Dreiser, Jan [3 ,5 ]
Piamonteze, Cinthia [5 ]
Nolting, Frithjof [5 ]
Gangopadhyay, Shruba [1 ]
Albertini, Oliver R. [1 ,6 ]
Macfarlane, Roger M. [1 ]
Lutz, Christopher P. [1 ]
Jones, Barbara A. [1 ]
Gambardella, Pietro [4 ]
Heinrich, Andreas J. [1 ]
Brune, Harald [3 ]
机构
[1] IBM Almaden Res Ctr, San Jose, CA 95120 USA
[2] Univ Basel, Dept Phys, CH-4056 Basel, Switzerland
[3] Ecole Polytech Fed Lausanne, Inst Condensed Matter Phys, Stn 3, CH-1015 Lausanne, Switzerland
[4] ETH, Dept Mat, CH-8093 Zurich, Switzerland
[5] Paul Scherrer Inst, Swiss Light Source, CH-5232 Villigen, Switzerland
[6] Georgetown Univ, Dept Phys, Washington, DC 20057 USA
基金
美国国家科学基金会; 瑞士国家科学基金会;
关键词
RAY CIRCULAR-DICHROISM; PERPENDICULAR-ANISOTROPY; SPECTROSCOPY; ABSORPTION; RESOLUTION; SURFACE; MOMENT;
D O I
10.1126/science.1252841
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Designing systems with large magnetic anisotropy is critical to realize nanoscopic magnets. Thus far, the magnetic anisotropy energy per atom in single-molecule magnets and ferromagnetic films remains typically one to two orders of magnitude below the theoretical limit imposed by the atomic spin-orbit interaction. We realized the maximum magnetic anisotropy for a 3d transition metal atom by coordinating a single Co atom to the O site of an MgO(100) surface. Scanning tunneling spectroscopy reveals a record-high zero-field splitting of 58 millielectron volts as well as slow relaxation of the Co atom's magnetization. This striking behavior originates from the dominating axial ligand field at the O adsorption site, which leads to out-of-plane uniaxial anisotropy while preserving the gas-phase orbital moment of Co, as observed with x-ray magnetic circular dichroism.
引用
收藏
页码:988 / 992
页数:5
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