Tunable magnetism on Si (111 ) - (2×1 ) via chemisorption of graphene nanoribbons

Zhuhua Zhang, Wanlin Guo, Xiao Cheng Zeng

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

We demonstrate from density-functional theory calculations that strong spin polarization can be achieved on a silicon surface via chemisorption of graphene nanoribbons (GNRs). The net electron spins are due to the unique silicon dangling-bond states induced by the chemisorption of GNRs and further localized by the well-aligned Si-C bonds between the silicon surface and the GNRs. The induced magnetic moment on the silicon surface depends on the width of GNRs and is thus tunable through controlling lateral separation among GNRs. We show that the silicon surface magnetization can even sustain large vertical compression to the GNRs and thus can be used as a functional switch upon high deformation of GNR. Similar magnetic behavior can be also achieved via chemisorption of certain organic molecules on the silicon surface. Our finding points to a viable nanofabrication approach to achieve intrinsic spin polarization on silicon nanostructure, thereby having implications in the emerging field of silicon-based spintronics.

Original languageEnglish (US)
Article number235423
JournalPhysical Review B - Condensed Matter and Materials Physics
Volume82
Issue number23
DOIs
StatePublished - Dec 13 2010

Fingerprint

Nanoribbons
Carbon Nanotubes
Graphite
Magnetism
Silicon
Chemisorption
chemisorption
Graphene
graphene
silicon
Spin polarization
Magnetoelectronics
Dangling bonds
nanofabrication
polarization
Magnetic moments
Nanotechnology
electron spin
Density functional theory
emerging

ASJC Scopus subject areas

  • Electronic, Optical and Magnetic Materials
  • Condensed Matter Physics

Cite this

Tunable magnetism on Si (111 ) - (2×1 ) via chemisorption of graphene nanoribbons. / Zhang, Zhuhua; Guo, Wanlin; Zeng, Xiao Cheng.

In: Physical Review B - Condensed Matter and Materials Physics, Vol. 82, No. 23, 235423, 13.12.2010.

Research output: Contribution to journalArticle

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