4.8 Article

Graphene nanoribbon blends with P3HT for organic electronics

Journal

NANOSCALE
Volume 6, Issue 12, Pages 6301-6314

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c4nr00256c

Keywords

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Funding

  1. EC - Marie-Curie ITNs GENIUS [PITN-GA-2010-264694]
  2. EC - Marie-Curie ITNs SUPERIOR [PITN-GA-2009-238177]
  3. Graphene Flagship [GA-604391]
  4. International Center for Frontier Research in Chemistry (icFRC)
  5. Marie Curie project [PIEF-GA-2009-253521]
  6. statutory activity subsidy for the Faculty of Chemistry of Wroclaw University of Technology
  7. ERC Grant NANOPOTS
  8. ERC Grant Hetero2D
  9. EPSRC [EP/K01711X/1, EP/K017144/1, EP/L016087/1]
  10. EU grant CARERAMM
  11. MEM4WIN
  12. Royal Society Wolfson Research Merit Award
  13. Villum Foundation under the Young Investigator Programme [VKR023122]
  14. EPSRC [EP/K01711X/1, EP/K017144/1] Funding Source: UKRI
  15. Engineering and Physical Sciences Research Council [EP/K017144/1, EP/K01711X/1] Funding Source: researchfish
  16. Villum Fonden [00007271] Funding Source: researchfish

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In organic field-effect transistors (OFETs) the electrical characteristics of polymeric semiconducting materials suffer from the presence of structural/morphological defects and grain boundaries as well as amorphous domains within the film, hindering an efficient transport of charges. To improve the percolation of charges we blend a regioregular poly(3-hexylthiophene) (P3HT) with newly designed N = 18 armchair graphene nanoribbons (GNRs). The latter, prepared by a bottom-up solution synthesis, are expected to form solid aggregates which cannot be easily interfaced with metallic electrodes, limiting charge injection at metal-semiconductor interfaces, and are characterized by a finite size, thus by grain boundaries, which negatively affect the charge transport within the film. Both P3HT and GNRs are soluble/dispersible in organic solvents, enabling the use of a single step co-deposition process. The resulting OFETs show a three-fold increase in the charge carrier mobilities in blend films, when compared to pure P3HT devices. This behavior can be ascribed to GNRs, and aggregates thereof, facilitating the transport of the charges within the conduction channel by connecting the domains of the semiconductor film. The electronic characteristics of the devices such as the I-on/I-off ratio are not affected by the addition of GNRs at different loads. Studies of the electrical characteristics under illumination for potential use of our blend films as organic phototransistors (OPTs) reveal a tunable photoresponse. Therefore, our strategy offers a new method towards the enhancement of the performance of OFETs, and holds potential for technological applications in (opto)electronics.

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