Bulk heterojunction (BHJ) solar cells composed of conjugated polymer-fullerene blends currently display power conversion efficiencies (PCEs) in the range of 6–8%. However, PCE and processing depend on batch variations in solubility, molecular weight, polydispersity, and purity. These problems are absent with solution-processed, small-molecule (SM) BHJ solar cells where the higher degree of molecular precision circumvents the statistical variability of polymers. To date, reported PCEs of SM BHJ solar cells have ranged from 2% to 5%. Recently, however, G.C. Bazan, A.J. Heeger, and co-researchers from the University of California–Santa Barbara, used rational molecular design and an unconventional processing method to fabricate SM BHJ solar cells with a PCE of 6.7%.
Bazan, Heeger, and co-researchers report their synthesis of a new small-molecule donor, DTS(PTTh2)2 (see Figure) in the November 6, 2011 online edition of Nature Materials (DOI: 10.1038/NMAT3160). Based on a core acceptor/donor/acceptor framework with donor end-capping units, DTS(PTTh2)2 displays excellent solubility in organic solvents, strong optical absorption from 600 nm to 800 nm, and a field-effect hole mobility of ∼0.1 cm2V–1s–1.
The planarity of DTS(PTTh2)2 was designed to increase charge-carrier mobilities by promoting intramolecular π-delocalization and intermolecular π-π-stacking, and the substituted bithiophene end caps serve both to extend π-conjugation and improve film formation. In fact, the absorption peak for the cast thin film is red-shifted with respect to DTS(PTTh2)2 in solution, which is consistent with an ordered structure and an optical bandgap of ∼1.5 eV.
The molecular structure for (a) the small-molecule donor: 5,5´-bis{(4-(7-hexylthiophen-2-yl)thiophen-2-yl)-[1,2,5]thiadiazolo[3,4-c]pyridine}-3,3´-di-2-ethylhexylsilylene2,2´-bithiophene, abbreviated DTS(PTTh2)2; and (b) the [6,6]-phenyl C70-butyric acid methyl ester, abbreviated PC70BM. Reproduced with permission from Nature Mater. (2011), DOI: 10.1038/NMAT3160. © 2011 Macmillan Publishers Ltd.
The researchers investigated photovoltaic characteristics using a conventional layered architecture, ITO/MoOx/ DTS(PTTh2)2:PC70BM, where ITO is indium tin oxide, MoOx is a molybdenum oxide anode, and PC70BM is [6,6]-phenyl C70-butyric acid methyl ester (see Figure). The DTS(PTTh2)2:PC70BM ratio of 70:30 displayed the highest PCE (4.5%). Solar cells with the most successful compositions displayed a maximum incident photon conversion efficiency of 68% at about 600 nm.
The researchers also found that 1,8-diiodooctane (DIO), which is commonly added to the solutions from which polymer BHJ layers are cast, actually decreases device performance at a concentration typically used for polymer films but increases performance at lower concentrations. DIO also alters the nano-morphology of the BHJ blend. The BHJ films cast with 0.25% v/v DIO have 15–20 nm domains, while films cast without DIO have 20–30 nm domains, with lattice planes covering a significant fraction of both films. The researchers inferred crystal overlap from the presence of overlapping planes, and postulated that smaller domains result in more efficient charge-carrier generation due to larger donor–acceptor interface areas.
The researchers said that their results “provide important progress for solution-processed organic solar cells, and demonstrate that such solar cells fabricated from small donor molecules can be competitive with their polymeric counterparts.”
