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Efficiency of Charge-Transfer Doping in Organic Semiconductors Probed with Quantitative Microwave and Direct-Current Conductance.
Ferguson, Andrew J; Reid, Obadiah G; Nanayakkara, Sanjini U; Ihly, Rachelle; Blackburn, Jeffrey L.
Affiliation
  • Ferguson AJ; National Renewable Energy Laboratory , Golden , Colorado 80401 , United States.
  • Reid OG; National Renewable Energy Laboratory , Golden , Colorado 80401 , United States.
  • Nanayakkara SU; Renewable and Sustainable Energy Institute , University of Colorado Boulder , Boulder , Colorado 80303 , United States.
  • Ihly R; National Renewable Energy Laboratory , Golden , Colorado 80401 , United States.
  • Blackburn JL; National Renewable Energy Laboratory , Golden , Colorado 80401 , United States.
J Phys Chem Lett ; 9(23): 6864-6870, 2018 Dec 06.
Article in En | MEDLINE | ID: mdl-30457866
Although molecular charge-transfer doping is widely used to manipulate carrier density in organic semiconductors, only a small fraction of charge carriers typically escape the Coulomb potential of dopant counterions to contribute to electrical conductivity. Here, we utilize microwave and direct-current (DC) measurements of electrical conductivity to demonstrate that a high percentage of charge carriers in redox-doped semiconducting single-walled carbon nanotube (s-SWCNT) networks is delocalized as a free carrier density in the π-electron system (estimated as >46% at high doping densities). The microwave and four-point probe conductivities of hole-doped s-SWCNT films quantitatively match over almost 4 orders of magnitude in conductance, indicating that both measurements are dominated by the same population of delocalized carriers. We address the relevance of this surprising one-to-one correspondence by discussing the degree to which local environmental parameters (e.g., tube-tube junctions, Coulombic stabilization, and local bonding environment) may impact the relative magnitudes of each transport measurement.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Phys Chem Lett Year: 2018 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Phys Chem Lett Year: 2018 Document type: Article Affiliation country: Country of publication: