Low- k amorphous fluorinated polymers such as poly(perfluoroalkenylvinyl ether) (CYTOP) have widely been used as gate dielectrics for organic field-effect transistors (OFETs) because of their strong hydrophobicity to prevent the penetration of moisture and other contaminants and their perfect solvent orthogonality with organic semiconductors. Here, we report a new functionality of the fluorinated low- k polymer dielectrics, which is spontaneous p doping at the dielectric-semiconductor interface in OFETs. This functionality makes the ambipolar charge transport a unipolar p type. In the OFETs based on indacenodithiophene- co-benzothiadiazole and diketopyrrolopyrrole-thieno[3,2- b]thiophene, the charge transport is obviously ambipolar when paired with common polymer dielectrics such as poly(methyl methacrylate); however, it is perfectly modulated to the unipolar p type by applying the fluorinated dielectrics of CYTOP and poly(tetrafluoroethylene) (Teflon). We propose that this modulation of charge transport results from the rearrangement of C-F bonds at the interface between the fluorine-containing dielectrics and the conjugated polymer semiconductors by proper thermal annealing. These well-aligned dipole moments lead to an abrupt downshift of the Fermi level of the semiconductor toward the highest occupied molecular orbitals near the dielectric-semiconductor interface, which provides a p-doping effect on the channel transport and results in unipolar p-type characteristics in the composed OFETs. This study reveals a new functionality of the fluorinated dielectrics for future organic electronics.
Keywords: amorphous polymer; charge carrier transport; doping effect; fluorinated low-k gate dielectric; organic field-effect transistors.