4.8 Article

Imaging and Tuning Molecular Levels at the Surface of a Gated Graphene Device

期刊

ACS NANO
卷 8, 期 6, 页码 5395-5401

出版社

AMER CHEMICAL SOC
DOI: 10.1021/nn501459v

关键词

graphene; organic molecules; vibronic levels; scanning tunneling microscopy; scanning tunneling spectroscopy; density functional theory; GW self-energy

资金

  1. Nanomachine program at the Lawrence Berkeley National Laboratory - Office of Science, Office of Basic Energy Sciences of the US Department of Energy [DE-AC02-05CH11231]
  2. National Science Foundation [DMR-1235361, DMR10-1006184, EEC-0832819]
  3. Austrian Science Fund (FWF) [J3026-N16]
  4. Singapore grant Novel 2D materials with tailored properties: beyond graphene [R-144-000-295-281]
  5. Simons Foundation Fellowship in Theoretical Physics
  6. Department of Defense (DoD) through National Defense Science & Engineering Graduate Fellowship (NDSEG) Program
  7. National Science Foundation
  8. Office of Science, Office of Basic Energy Sciences, of the US Department of Energy [DE-AC02-05CH11231]
  9. Austrian Science Fund (FWF) [J3026] Funding Source: Austrian Science Fund (FWF)
  10. Directorate For Engineering [1235361] Funding Source: National Science Foundation
  11. Div Of Civil, Mechanical, & Manufact Inn [1235361] Funding Source: National Science Foundation
  12. Austrian Science Fund (FWF) [J 3026] Funding Source: researchfish

向作者/读者索取更多资源

Gate-controlled tuning of the charge carrier density in graphene devices provides new opportunities to control the behavior of molecular adsorbates. We have used scanning tunneling microscopy (STM) and spectroscopy (STS) to show how the vibronic electronic levels of 1,3,5-tris(2,2-dicyanovinyl)benzene molecules adsorbed onto a graphene/BN/SiO2 device can be tuned via application of a backgate voltage. The molecules are observed to electronically decouple from the graphene layer, giving rise to well-resolved vibronic states in dI/dV spectroscopy at the single-molecule level. Density functional theory (DFT) and many-body spectral function calculations show that these states arise from molecular orbitals coupled strongly to carbon-hydrogen rocking modes. Application of a back-gate voltage allows switching between different electronic states of the molecules for fixed sample bias.

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