Closely packed, low reorganization energy p-extended postfullerene acceptors for efficient polymer solar cells

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 115; no. 36; p. E8341
• Main Authors: Swick, Steven M, Zhu, Weigang, Matta, Micaela, Aldrich, Thomas J, Harbuzaru, Alexandra, Lopez Navarrete, J Teodomiro, Ortiz, Rocio Ponce, Kohlstedt, Kevin L, Schatz, George C, Facchetti, Antonio, Melkonyan, Ferdinand S, Marks, Tobin J
• Format: Journal Article
• Language: English
• Published: Washington National Academy of Sciences 04-09-2018
• Subjects: Atomic force microscopy; Calorimetry; Charge transport; Chemical analysis; Coupling (molecular); Data processing; Density functional theory; Differential scanning calorimetry; Electronic structure; Electronics industry; Electrons; Energy conversion efficiency; Evaporation; Fluoropolymers; Fullerenes; Methylene; Microscopy; Molecular orbitals; Molecular structure; Optoelectronics; Organic chemistry; Organic semiconductors; Photovoltaic cells; Photovoltaics; Polymers; Quantum chemistry; Single crystals; Solar cells; Solar energy; Spectroscopy; Spectrum analysis; Thermogravimetric analysis; X-ray diffraction; X-ray scattering
• ISSN: 0027-8424; 1091-6490

New organic semiconductors are essential for developing inexpensive, high-efficiency, solution-processable polymer solar cells (PSCs). PSC photoactive layers are typically fabricated by film-casting a donor polymer and a fullerene acceptor blend, with ensuing solvent evaporation and phase separation creating discrete conduits for photogenerated holes and electrons. Until recently, n-type fullerene acceptors dominated the PSC literature; however, indacenodithienothiophene (IDTT)-based acceptors have recently enabled remarkable PSC performance metrics, for reasons that are not entirely obvious. We report two isomeric IDTT-based acceptors 3,9-bis(2-methylene-(3-(1,1-dicyanomethylene)-benz-(5, 6)indanone))-5,5,11,11-tetrakis(4-nonylphenyl)-dithieno[2,3-d:2′,3′-d′]-s-indaceno[1,2-b:5,6-b′]di-thiophene (ITN-C9) and 3,9-bis(2-methylene-(3-(1,1-dicyanomethylene)-benz(6,7)indanone))-5,5,11,11-tetrakis(4-nonylphenyl)-dithieno[2,3-d:2′,3′-d′]-s-indaceno[1,2-b:5,6-b′]dithiophene (ITzN-C9) that shed light on the exceptional IDTT properties vis-à-vis fullerenes. The neat acceptors and blends with fluoropolymer donor poly{[4,8-bis[5-(2- ethylhexyl)-4-fluoro-2-thienyl]benzo[1,2-b:4,5-b′]dithiophene2,6-diyl]-alt-[2,5-thiophenediyl[5,7-bis(2-ethylhexyl)-4,8-dioxo4H,8H-benzo[1,2-c:4,5-c′]dithiophene-1,3-diyl]]} (PBDB-TF) are investigated by optical spectroscopy, cyclic voltammetry, thermogravimetric analysis, differential scanning calorimetry, single-crystal X-ray diffraction, photovoltaic response, space-charge-limited current transport, atomic force microscopy, grazing incidence wide-angle X-ray scattering, and density functional theory-level quantum chemical analysis. The data reveal that ITN-C9 and ITzN-C9 organize such that the lowest unoccupied molecular orbital-rich end groups have intermolecular π−π distances as close as 3.31(1) Å, with electronic coupling integrals as large as 38 meV, and internal reorganization energies as small as 0.133 eV, comparable to or superior to those in fullerenes. ITN-C9 and ITzN-C9 have broad solar-relevant optical absorption, and, when blended with PBDB-TF, afford devices with power conversion efficiencies near 10%. Performance differences between ITN-C9 and ITzN-C9 are understandable in terms of molecular and electronic structure distinctions via the influences on molecular packing and orientation with respect to the electrode.