Synergetic Solvent Engineering of Film Nanomorphology to Enhance Planar Perylene Diimide-Based Organic Photovoltaics

Solvent additive has proven as a useful protocol for improving the film nanomorphology of polymer donor (D): fullerene acceptor (A) blends in bulk heterojunction (BHJ) photovoltaic cells. By contrast, the effect of such solvent additive on nonfullerene BHJ cells based on perylene diimide acceptor, for instance, is less effective because of their highly planar structure and strong π-aggregation in solid state. Here we choose N,N′-bis­(1-ethylpropyl)-perylene-3,4,9,10-tetracarboxylic diimide (PDI) and thieno­[3,4-b]­thiophene-alt-benzodithiophene (PTB7) as a model D:A blend system to investigate how solvent engineering strategy synergistically impacts the blend film nanomorphology. Based on the differences of solvent volatility and solubility, various host solventschloroform (CF) and chlorobenzene (CB) and solvent additiveschloronaphthalene (CN) and 1,8-diiodooctane (DIO) are selected for comparative studies. It is found that the π-aggregation of PDIs can be largely suppressed by using low-boiling point (T b) CF solvent, yet enlarged by using high-T b CB. Moreover, CN additive provides good solubility of PDI molecules and hence reduces large PDI aggregates in CB system, while DIO exhibiting poor solubility works oppositely. By contrast, DIO that presents larger T b difference with CF prolongs the film-forming, which assists in optimizing the PDI aggregation and increases the intermixed PTB7:PDI phases more significantly than CN in CF system, yielding the finest phase-separation morphology and balanced charge mobility. Consequently, the inverted BHJ cells based on CF-processed PTB7:PDI blend film with 0.4 vol % DIO exhibit the highest PCE of 3.55% with a fill factor of 56%, both of which are among the best performance for such a paradigm PTB7:PDI blend-based BHJ cells.