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Polaron hopping mediated by nuclear tunnelling in semiconducting polymers at high carrier density

Author

Listed:
  • Kamal Asadi

    (Philips Research Laboratories)

  • Auke J. Kronemeijer

    (Cavendish Laboratory, University of Cambridge)

  • Tobias Cramer

    (CNR, Institute for the Study of Nanostructured Materials)

  • L. Jan Anton Koster

    (Zernike Institute for Advanced Materials, University of Groningen)

  • Paul W. M. Blom

    (Zernike Institute for Advanced Materials, University of Groningen
    Max-Planck Institute for Polymer Research)

  • Dago M. de Leeuw

    (Zernike Institute for Advanced Materials, University of Groningen
    Max-Planck Institute for Polymer Research)

Abstract

The transition rate for a single hop of a charge carrier in a semiconducting polymer is assumed to be thermally activated. As the temperature approaches absolute zero, the predicted conductivity becomes infinitesimal in contrast to the measured finite conductivity. Here we present a uniform description of charge transport in semiconducting polymers, including the existence of absolute-zero ground-state oscillations that allow nuclear tunnelling through classical barriers. The resulting expression for the macroscopic current shows a power-law dependence on both temperature and voltage. To suppress the omnipresent disorder, the predictions are experimentally verified in semiconducting polymers at high carrier density using chemically doped in-plane diodes and ferroelectric field-effect transistors. The renormalized current-voltage characteristics of various polymers and devices at all temperatures collapse on a single universal curve, thereby demonstrating the relevance of nuclear tunnelling for organic electronic devices.

Suggested Citation

  • Kamal Asadi & Auke J. Kronemeijer & Tobias Cramer & L. Jan Anton Koster & Paul W. M. Blom & Dago M. de Leeuw, 2013. "Polaron hopping mediated by nuclear tunnelling in semiconducting polymers at high carrier density," Nature Communications, Nature, vol. 4(1), pages 1-8, June.
  • Handle: RePEc:nat:natcom:v:4:y:2013:i:1:d:10.1038_ncomms2708
    DOI: 10.1038/ncomms2708
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    Cited by:

    1. Chiara Labanti & Jiaying Wu & Jisoo Shin & Saurav Limbu & Sungyoung Yun & Feifei Fang & Song Yi Park & Chul-Joon Heo & Younhee Lim & Taejin Choi & Hyeong-Ju Kim & Hyerim Hong & Byoungki Choi & Kyung-B, 2022. "Light-intensity-dependent photoresponse time of organic photodetectors and its molecular origin," Nature Communications, Nature, vol. 13(1), pages 1-10, December.

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