Picene and PTCDI based solution processable ambipolar OFETs.

ABSTRACT: Facile and efficient solution-processed bottom gate top contact organic field-effect transistor was fabricated by employing the active layer of picene (donor, D) and N,N'-di(dodecyl)-perylene-3,4,9,10-tetracarboxylic diimide (acceptor, A). Balanced hole (0.12 cm²/Vs) and electron (0.10 cm²/Vs) mobility with I_on/off of 10⁴ ratio were obtained for 1:1 ratio of D/A blend. On increasing the ratio of either D or A, the charge carrier mobility and I_on/off ratio improved than that of the pristine molecules. Maximum hole (µ_max,h) and electron mobilities (µ_max,e) were achieved up to 0.44 cm²/Vs for 3:1 and 0.25 cm²/Vs for 1:3, (D/A) respectively. This improvement is due to the donor phase function as the trap center for minority holes and decreased trap density of the dielectric layer, and vice versa. High ionization potential (- 5.71 eV) of 3:1 and lower electron affinity of (- 3.09 eV) of 1:3 supports the fine tuning of frontier molecular orbitals in the blend. The additional peak formed for the blends at high negative potential of - 1.3 V in cyclic voltammetry supports the molecular level electronic interactions of D and A. Thermal studies supported the high thermal stability of D/A blends and SEM analysis of thin films indicated their efficient molecular packing. Quasi-?-? stacking owing to the large ? conjugated plane and the crystallinity of the films are well proved by GIXRD. DFT calculations also supported the electronic distribution of the molecules. The electron density of states (DOS) of pristine D and A molecules specifies the non-negligible interaction coupling among the molecules. This D/A pair has unlimited prospective for plentiful electronic applications in non-volatile memory devices, inverters and logic circuits.

SUBMITTER: Balambiga B 

PROVIDER: S-EPMC7744517 | biostudies-literature | 2020 Dec

REPOSITORIES: biostudies-literature