Functional p-type, polymerized organic electrode interlayer in CH3NH3PbI3 perovskite/fullerene planar heterojunction hybrid solar cells.

Thermal curing of the styrene-functionalized 9,9-diarylfluorene-based triaryldiamine monomer (VB-DAAF) forms an ideal p-type organic electrode interlayer capable of resisting solvation of the polar precursor solution in fabricating methylammonium lead iodide (CH3NH3PbI3) perovskite/fullerene (C-60) planar heterojunction hybrid solar cells. The polymerized VB-DAAF film exhibits a good energy level alignment with the valence-band-edge level of the CH3NH3PbI3 perovskite to facilitate the transport of holes. The large energy barrier to the conduction-band-edge level of the CH3NH3PbI3 perovskite effectively blocks electrons from reaching the positive electrode and reduces the photon energy loss due to recombination. The best-performing cell with the configuration of glass/indium tin oxide/polymerized VB-DAAF/CH3NH3PbI3 perovskite/C-60/bathocuproine/aluminum is free of a poly(34-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) layer to achieve an open-circuit voltage (V-OC) = 1.02 V, a short-circuit current (J(SC)) = 18.92 mA/cm(2), and a fill factor (FF) = 0.78, corresponding to a power conversion efficiency (PCE) of 15.17% under standard 1 sun AM 1.5G simulated solar irradiation. The performance is much superior to the device applying the PEDOT:PSS interlayer with photovoltaic parameters of V-OC = 0.85 V, J(SC) = 16.37 mA/cm(2), and FF = 0.74, corresponding to a PCE of 10.27%. Additionally, we had applied a UV-assisted process to polymerize the VB-DAAF film at relatively lower temperature and fabricate decent perovskite-based solar cells on the flexible substrate for real applications.