Improving the Photovoltaic Performance of Dithienobenzodithiophene-Based Polymers via Addition of an Additional Eluent in the Soxhlet Extraction Process.

Dithieno[2,3- d ;2',3'- d ']benzo[1,2- b ;4,5- b ']dithiophene (DTBDT) is a kind of pentacyclic aromatic electron-donating unit with unique optoelectronic properties, but it has received less attention in the design of photovoltaic polymers. In this work, we copolymerized DTBDT with the electron-deficient unit of dithieno[3',2':3,4;2″,3″:5,6]benzo[1,2- c ][1,2,5]thiadiazole (DTBT) and obtained two polymers, PE55 and PE56 , with a synergistic heteroatom substitution strategy. When blended with the classic nonfullerene acceptor Y6 , PE55 and PE56 achieve power conversion efficiencies (PCEs) of 13.78% and 14.49%, respectively, which indicates that the introduction of sulfur atoms on the conjugated side chain of the D unit is a promising method to enhance the performance of DTBDT-based polymers. Besides, we utilize dichloromethane and chloroform to separate the low molecular weight (Mw) fractions in the solvent extraction process to obtain PE55-CF and PE56-CB , and the PCEs are further improved to 15.00% and 16.11%, respectively. The stronger π-π stacking, optimized blend film morphology, and higher charge mobilities contribute to the enhanced PCEs for polymers with higher Mw obtained via the multistep solvent extraction strategy. Our results not only provide a simple and effective way to improve the photovoltaic performance of conjugated polymers but also imply that some reported polymers purified from the traditional one-step solvent extraction method might be seriously underestimated.