Colossal enhancement of spin-orbit coupling in weakly hydrogenated graphene

被引:354
作者
Balakrishnan, Jayakumar [1 ,2 ]
Koon, Gavin Kok Wai [1 ,2 ,3 ]
Jaiswal, Manu [1 ,2 ]
Castro Neto, A. H. [1 ,2 ,4 ]
Oezyilmaz, Barbaros [1 ,2 ,3 ,4 ]
机构
[1] Natl Univ Singapore, Dept Phys, Singapore 117542, Singapore
[2] Natl Univ Singapore, Graphene Res Ctr, Singapore 117546, Singapore
[3] Natl Univ Singapore, Nanocore, Singapore 117546, Singapore
[4] Ctr Life Sci CeLS, NUS Grad Sch Integrat Sci & Engn NGS, Singapore 117456, Singapore
基金
新加坡国家研究基金会;
关键词
CARBON NANOTUBES; HALL; SEMICONDUCTORS; ELECTRONS; DEVICES;
D O I
10.1038/nphys2576
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
Graphene's extremely small intrinsic spin-orbit (SO) interaction(1) makes the realization of many interesting phenomena such as topological/quantum spin Hall states(2,3) and the spin Hall effect(4) (SHE) practically impossible. Recently, it was predicted(1,5-7) that the introduction of adatoms in graphene would enhance the SO interaction by the conversion of sp(2) to sp(3) bonds. However, introducing adatoms and yet keeping graphene metallic, that is, without creating electronic (Anderson) localization(8), is experimentally challenging. Here, we show that the controlled addition of small amounts of covalently bonded hydrogen atoms is sufficient to induce a colossal enhancement of the SO interaction by three orders of magnitude. This results in a SHE at zero external magnetic fields at room temperature, with non-local spin signals up to 100 Omega; orders of magnitude larger than in metals(9). The non-local SHE is, further, directly confirmed by Larmor spin-precession measurements. From this and the length dependence of the non-local signal we extract a spin relaxation length of similar to 1 mu m, a spin relaxation time of similar to 90 ps and a SO strength of 2.5 meV.
引用
收藏
页码:284 / 287
页数:4
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