4.6 Article

Reorientation of π-conjugated molecules on few-layer MoS2 films

Journal

PHYSICAL CHEMISTRY CHEMICAL PHYSICS
Volume 22, Issue 5, Pages 3097-3104

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c9cp05728e

Keywords

-

Funding

  1. DAAD/SAV grant
  2. DFG
  3. Research & Innovation Operational Programme - ERDF [313021T081]
  4. Alexander von Humboldt foundation
  5. [APVV-17-0352]
  6. [APVV-16-0319]
  7. [APVV-15-0641]
  8. [APVV-15-0693]
  9. [APVV-14-0745]
  10. [SK-CN-RD-18-0006]
  11. [VEGA 2/0092/18]
  12. [VEGA 2/0149/17]
  13. [ITMS 26230120002]
  14. [ITMS 26210120002]

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Small pi-conjugated organic molecules have attracted substantial attention in the past decade as they are considered as candidates for future organic-based (opto-)electronic applications. The molecular arrangement in the organic layer is one of the crucial parameters that determine the efficiency of a given device. The desired orientation of the molecules is achieved by a proper choice of the underlying substrate and growth conditions. Typically, one underlying material supports only one inherent molecular orientation at its interface. Here, we report on two different orientations of diindenoperylene (DIP) molecules on the same underlayer, i.e. on a few-layer MoS2 substrate. We show that DIP molecules adopt a lying-down orientation when deposited on few-layer MoS2 with horizontally oriented layers. In contrast, for vertically aligned MoS2 layers, DIP molecules are arranged in a standing-up manner. Employing in situ and real-time grazing-incidence wide-angle X-ray scattering (GIWAXS), we monitored the stress evolution within the thin DIP layer from the early stages of the growth, revealing different substrate-induced phases for the two molecular orientations. Our study opens up new possibilities for the next-generation of flexible electronics, which might benefit from the combination of MoS2 layers with unique optical and electronic properties and an extensive reservoir of small organic molecules.

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