Breaking time-reversal symmetry at the topological insulator surface by metal-organic coordination networks

被引:18
|
作者
Otrokov, M. M. [1 ,2 ,3 ]
Chulkov, E. V. [1 ,3 ,4 ,5 ]
Arnau, A. [1 ,4 ,5 ]
机构
[1] DIPC, San Sebastian 20018, Spain
[2] Tomsk State Univ, Tomsk 634050, Russia
[3] St Petersburg State Univ, St Petersburg 198504, Russia
[4] Ctr Fis Mat CFM MPC, Dept Fis Mat UPV EHU, San Sebastian 20080, Spain
[5] Ctr Mixto CSIC UPV EHU, San Sebastian 20080, Spain
关键词
CHARGE-TRANSFER; AB-INITIO; MEDIATED FERROMAGNETISM; MAGNETIC ORDER; DIRAC-FERMION; ANISOTROPY; ELECTRON; STATE; DISORDER; ATOMS;
D O I
10.1103/PhysRevB.92.165309
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
We propose a way to break the time-reversal symmetry at the surface of a three-dimensional topological insulator that combines features of both surface magnetic doping and magnetic proximity effect. Based on the possibility of organizing an ordered array of local magnetic moments by inserting them into a two-dimensional matrix of organic ligands, we study the magnetic coupling and electronic structure of such metal-organic coordination networks on a topological insulator surface from first principles. In this way, we find that both Co and Cr centers, linked by the tetracyanoethylenelike organic ligand, are coupled ferromagnetically and, depending on the distance to the topological insulator substrate, can yield a magnetic proximity effect. This latter leads to the Dirac point gap opening indicative of the time-reversal symmetry breaking.
引用
收藏
页数:9
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