4.8 Article

Weak screening of a large dipolar molecule adsorbed on graphene

期刊

CARBON
卷 50, 期 5, 页码 1981-1986

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.carbon.2011.12.055

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资金

  1. Semiconductor Research Corporation, Division of Nanomanufacturing Sciences [2123.001]
  2. National Science Foundation [CHE-0909580, NSF-MRI 0923021, PHY-1005071]
  3. Nebraska MRSEC [DMR-0820521]
  4. Centre National de la Recherche Scientifique
  5. Ministere de la Recherche et des Nouvelles Technologies
  6. ANR [07-BLAN-0274-04]
  7. Nebraska Center for Materials and Nanoscience at University of Nebraska-Lincoln
  8. National Research Foundation of Korea (NRF)
  9. Ministry of Education, Science and Technology [2010-0005706]
  10. Direct For Mathematical & Physical Scien
  11. Division Of Chemistry [0909580] Funding Source: National Science Foundation
  12. Division Of Materials Research
  13. Direct For Mathematical & Physical Scien [0851703] Funding Source: National Science Foundation
  14. Office Of The Director
  15. Office of Integrative Activities [1002410] Funding Source: National Science Foundation
  16. National Research Foundation of Korea [2010-0005706] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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We compare the electronic structure of a quinonoid zwitterionic type molecule adsorbed on both gold and graphene on copper substrates. This (6Z)-4-(butylamino)-6-(butyliminio)-3-oxocyclohexa-1,4-dien-1-olate, C6H2(center dot center dot center dot NHR)(2)(center dot center dot center dot O)(2) where R = n-C4H9, film is made of small molecules with a large intrinsic dipole of 10 Debyes. We find that the photoemission and inverse photoemission final states are well screened for these dipolar molecules on gold. This is not observed when they are adsorbed on graphene on copper. This weaker screening results in a larger highest occupied molecular orbital to lowest unoccupied molecular orbital gap for the molecules on graphene. (C) 2012 Elsevier Ltd. All rights reserved.

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