Environmentally friendly and efficient organic photovoltaic (OPV) devices played a significantly essential role in commercial applications. Herein, The PM6:TBFCl50-BDD:IT-4F-based ternary device was fabricated by using non-halogen solvent o-xylene (o-XY), and...
In recent years, ternary organic photovoltaic cells (OPVs) have been dedicated to improving power conversion efficiency (PCE) by broadening optical absorption spectra. Ternary OPVs with different poly[thieno[3,2-b]thiophene-2,5-diyl-alt-4,9-bis(4-(2-decyltetradecyl)thien-2-yl)naphtho[1,2-c:5,6-c’]bis[1,2,5]thiadiazole-5,5′-diyl] (PTT-DTNT-DT) doping concentrations were designed and the effect of PTT-DTNT-DT as a complementary electron donor on the performance of OPVs was investigated. The optimized PCE of OPVs was increased from 3.42% to 4.66% by doping 20 wt % PTT-DTNT-DT. The remarkable improvement in the performance of the ternary device is mainly attributed to the sharp increase in the short-circuit current density and fill-factor. The major reasons have been systematically studied from atomic force microscopy, electrochemical impedance spectroscopy, surface energy, space charge limited current and photocurrent behavior. It has been found that the separation of excitons and the transportation of charge are enhanced while light absorption is increased, and the charge recombination also decreases due to the optimization of the cascade energy level and the morphology of the ternary active layer. The results show that it is feasible to improve the performance of ternary OPVs by their complementary absorption.
A novel (E)-5-(2-(5-alkylthiothiophen-2-yl)vinyl)thien-2-yl (TVT)-comprising benzo[1,2-b:4,5-b’]dithiophene (BDT) derivative (BDT-TVT) was designed and synthetized to compose two donor-acceptor (D-A) typed copolymers (PBDT-TVT-ID and PBDT-TVT-DTNT) with the electron-withdrawing unit isoindigo (ID) and naphtho[1,2-c:5,6-c′]bis[1,2,5]thiadiazole (NT), respectively. PBDT-TVT-ID and PBDT-TVT-DTNT showed good thermal stability (360 °C), an absorption spectrum from 300 nm to 760 nm and a relatively low lying energy level of Highest Occupied Molecular Orbital (EHOMO) (−5.36 to –5.45 eV), which could obtain a large open-circuit voltage (Voc) from photovoltaic devices with PBDT-TVT-ID or PBDT-TVT-DTNT. The photovoltaic devices with ITO/PFN/polymers: PC71BM/MoO3/Ag structure were assembled and exhibited a good photovoltaic performance with a power conversion efficiency (PCE) of 4.09% (PBDT-TVT-ID) and 5.44% (PBDT-TVT-DTNT), respectively. The best PCE of a PBDT-TVT-DTNT/PC71BM-based device mainly originated from its wider absorption, higher hole mobility and favorable photoactive layer morphology.
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