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Bottom-up organic integrated circuits

Abstract

Self-assembly—the autonomous organization of components into patterns and structures1—is a promising technology for the mass production of organic electronics. Making integrated circuits using a bottom-up approach involving self-assembling molecules was proposed2 in the 1970s. The basic building block of such an integrated circuit is the self-assembled-monolayer field-effect transistor (SAMFET), where the semiconductor is a monolayer spontaneously formed on the gate dielectric. In the SAMFETs fabricated so far, current modulation has only been observed in submicrometre channels3,4,5, the lack of efficient charge transport in longer channels being due to defects and the limited intermolecular π–π coupling between the molecules in the self-assembled monolayers. Low field-effect carrier mobility, low yield and poor reproducibility have prohibited the realization of bottom-up integrated circuits. Here we demonstrate SAMFETs with long-range intermolecular π–π coupling in the monolayer. We achieve dense packing by using liquid-crystalline molecules consisting of a π-conjugated mesogenic core separated by a long aliphatic chain from a monofunctionalized anchor group. The resulting SAMFETs exhibit a bulk-like carrier mobility, large current modulation and high reproducibility. As a first step towards functional circuits, we combine the SAMFETs into logic gates as inverters; the small parameter spread then allows us to combine the inverters into ring oscillators. We demonstrate real logic functionality by constructing a 15-bit code generator in which hundreds of SAMFETs are addressed simultaneously. Bridging the gap between discrete monolayer transistors and functional self-assembled integrated circuits puts bottom-up electronics in a new perspective.

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Figure 1: SAM microstructure.
Figure 2: Electrical SAMFET transport characteristics.
Figure 3: SAMFET inverter.
Figure 4: Integrated circuit.

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References

  1. Whitesides, G. M. & Grzybowski, B. Self-assembly at all scales. Science 295, 2418–2421 (2002)

    Article  ADS  CAS  Google Scholar 

  2. Aviram, A. & Ratner, M. A. Molecular rectifiers. Chem. Phys. Lett. 29, 277–283 (1974)

    Article  ADS  CAS  Google Scholar 

  3. Guo, X. et al. Chemoresponsive monolayer transistors. Proc. Natl Acad. Sci. USA 103, 11452–11456 (2006)

    Article  ADS  CAS  Google Scholar 

  4. Tulevski, G. S. et al. Attaching organic semiconductors to gate oxides: in situ assembly of monolayer field effect transistors. J. Am. Chem. Soc. 126, 15048–15050 (2004)

    Article  CAS  Google Scholar 

  5. Mottaghi, M. et al. Low-operating-voltage organic transistors made of bifunctional self-assembled monolayers. Adv. Funct. Mater. 17, 597–604 (2007)

    Article  CAS  Google Scholar 

  6. Onclin, S., Ravoo, B. J. & Reinhoudt, D. N. Engineering silicon oxide surfaces using self-assembled monolayers. Angew. Chem. Int. Edn 44, 6282–6304 (2005)

    Article  CAS  Google Scholar 

  7. Garnier, F. et al. Molecular engineering of organic semiconductors: design of self-assembly properties in conjugated thiophene oligomers. J. Am. Chem. Soc. 115, 8716–8721 (1993)

    Article  CAS  Google Scholar 

  8. Halik, M. et al. relationship between molecular structure and electrical performance of oligothiophene organic thin film transistors. Adv. Mater. 15, 917–922 (2003)

    Article  CAS  Google Scholar 

  9. van Breemen, A. J. J. M. et al. Large area liquid crystal monodomain field-effect transistors. J. Am. Chem. Soc. 128, 2336–2345 (2006)

    Article  CAS  Google Scholar 

  10. Ponomarenko, S. A. et al. Star-shaped oligothiophenes for solution-processible organic electronics: flexible aliphatic spacers approach. Chem. Mater. 18, 4101–4108 (2006)

    Article  CAS  Google Scholar 

  11. McCulloch, I. et al. Liquid-crystalline semiconducting polymers with high charge-carrier mobility. Nature Mater. 5, 328–333 (2006)

    Article  ADS  CAS  Google Scholar 

  12. Yoneda, Y. Anomalous surface reflection of X rays. Phys. Rev. 131, 2010–2013 (1963)

    Article  ADS  Google Scholar 

  13. Fenter, P. in Self-Assembled Monolayers of Thiols (ed. Uhlman, A.) 111–147 (Academic, 1991)

    Google Scholar 

  14. Fichou, D. Handbook of Oligo- and Polythiophenes (Wiley-VCH, 1999)

    Google Scholar 

  15. Melucci, M. et al. Multiscale self-organization of the organic semiconductor α-quinquethiophene. J. Am. Chem. Soc. 125, 10266–10274 (2003)

    Article  CAS  Google Scholar 

  16. Dinelli, F. et al. Spatially correlated charge transport in organic thin film transistors. Phys. Rev. Lett. 92, 116802 (2004)

    Article  ADS  Google Scholar 

  17. Ruiz, R., Papadimitratos, A., Mayer, A. C. & Malliaras, G. G. Thickness dependence of mobility in pentacene thin-film transistors. Adv. Mater. 17, 1795–1798 (2005)

    Article  CAS  Google Scholar 

  18. Park, B.-N. Seo, S. & Evans, P. G. Channel formation in single-monolayer pentacene thin film transistors. J. Phys. D 40, 3506–3511 (2007)

    Article  ADS  CAS  Google Scholar 

  19. Cantatore, E. & Meijer, E. J. in ESSCIRC ’03 29–36 (Proc. 29th Eur. Solid State Circuits Conf., IEEE, 2003)

    Google Scholar 

  20. Cantatore, E. et al. A 13.56-MHz RFID system based on organic transponders. IEEE J. Solid State Circuits. 42, 84–92 (2007)

    Article  ADS  Google Scholar 

Download references

Acknowledgements

We acknowledge H. Nulens and C. van der Marel for the AFM and X-ray photoemission spectroscopy measurements, M. Kaiser for the FIB-TEM analysis, A. P. Pleshkova for the mass spectrometry analysis, F. Zontone for technical assistance and N. Willard for discussions. We acknowledge financial support from the Dutch Polymer Institute, project 516, the EU project NAIMO (NMP4-CT-2004-500355), the Dutch Technology Foundation STW, the Austrian Science Foundation and H. C. Starck GmbH. We thank the European Synchrotron Research Facility for the use of the beamline ID10B.

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Correspondence to Stephan Kirchmeyer or Dago M. de Leeuw.

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This file contains Supplementary Information with Supplementary Figures S1-S31, Supplementary Tables S1-S4 and Supplementary References. (PDF 1273 kb)

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Smits, E., Mathijssen, S., van Hal, P. et al. Bottom-up organic integrated circuits. Nature 455, 956–959 (2008). https://doi.org/10.1038/nature07320

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