Abstract

The polaronic structures associated with the interchain stacking in the polymer semiconductor bulk or polymer semiconductor-dielectric interface in fully operational thiophene-based thin-film transistors (TFTs) were investigated with a newly developed in situ photoexcited charge collection spectroscopy (PECCS). The in situ PECCS spectra of polymer semiconductors exhibited the \ensuremath{\pi}-\ensuremath{\pi}${}^{*}$ absorption peaks between 2.05 and 2.45 eV, which were well-matched with those in the Ultraviolet-visible (UV-vis) absorption spectra of the corresponding polymer films. The spectra also showed associated charge-induced absorption peaks at 1.32, 1.39, 1.58, and 1.71 eV below the \ensuremath{\pi}-\ensuremath{\pi}${}^{*}$ absorption edge. These charge-induced absorption peaks might be related to the delocalized polaron states located in the both polymer semiconductor bulk and semiconductor-dielectric interface of our polymer-based TFTs. From the spectral results, we were able to extract the polaronic density of states (DOS) of the polymer channel, and we confirmed that the denser interchain packing in the polymer semiconductor channel leads to a larger DOS near the band edge, resulting in higher field-effect mobility.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.