RESUMEN
Large area (>20 cm × 2 cm)-oriented thin films of PQT-C12 with varying molecular weight and polydispersity index (PDI) were fabricated by the ribbon-shaped floating film transfer method aiming toward their application as an active semiconductor element of organic field effect transistors (OFETs). Investigation on the influence of the molecular weight and PDI upon the extent of molecular alignment and anisotropic charge transport was systematically carried out. It has been demonstrated that high molecular weight in combination with low PDI not only leads to a very high optical anisotropy >10 but also high charge carrier anisotropy with a hole mobility of about 0.07 cm2/V·s for OFETs using parallel-oriented PQT-C12 thin films. Such a structure-property correlation is highly beneficial for the development of high performance organic electronic devices by synergistic and amicable tuning of the optoelectronic anisotropies and polymer synthetic variables.
RESUMEN
Unavoidable defects in grain boundaries (GBs) are detrimental and critically influence the organometal halide perovskite performance and stability. To address this issue, semiconducting molecules have been employed to passivate traps along perovskite GBs. Here, we designed and synthesized three squaraine molecules (SQ) with zwitterionic structure to interact with under-coordinated Pb2+ and passivate Pb-I antisite defects. Density functional theory calculation shows symmetric O atoms could coordinate with perovskite grains simultaneously, resulting in continuous charge distribution at the SQ-perovskite interface. The energetic traps distribution in CH3NH3PbI3 perovskite is influenced significantly by the interaction between SQ and perovskite as analyzed by thermally stimulated current, in which the deep-level defects are considerably reduced due to efficient SQ passivation. In addition, we explore how SQ molecules with different energy offset affect the charge extraction, which is suggested to facilitate exciton separation at the perovskite-SQ interface. These benefits lead to enhanced perovskite efficiency from 15.77 to 18.83% with the fill factor approaching 80%, which is among the highest efficiency reported for MAPbI3 solar cells fabricated in an ambient environment at 60% relative humidity (RH). Considerable retardation of perovskite device degradation was achieved, retaining 90% of initial efficiency when kept 600 h at 60 ± 5% RH.
