4.7 Article

Multi-Sulfur-Annulated Fused Perylene Diimides for Organic Solar Cells with Low Open-Circuit Voltage Loss

Journal

ACS APPLIED ENERGY MATERIALS
Volume 2, Issue 5, Pages 3805-3814

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsaem.9b00492

Keywords

organic solar cell; nonfullerene acceptor; organic electronics; charge-transfer state; X-ray scattering

Funding

  1. National Key Basic Research Program of China (973 Program) [2014CB648300]
  2. National Natural Science Foundation of China [21422402, 21674050, 61136003]
  3. China Scholarship Council [201508320254]
  4. Virgil Elings
  5. Betty Elings Wells
  6. U.S. Department of Energy, Office of Science, Basic Energy Sciences [DESC-0012541]
  7. UCSB MRSEC [NSF DMR 1720256]

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Nonfullerene acceptors are important for increasing the power conversion efficiency of organic bulk heterojunction (BHJ) solar cells. The number of well performing nonfullerene acceptors is still relatively limited compared to the wide range of donor materials making it difficult to find donor-acceptor pairs with matching optical and electronic properties. We report the synthesis of three sulfur-annulated fused perylene diimide-based compounds (2PDI-2S, 2PDI-3S, and 2PDI-4S) that have varying electron affinity. BHJ solar cells with these acceptors and the donor polymer PTB7-Th have solar power conversion efficiencies above 5% with relatively high fill factors (>60%) for nonfullerene acceptors. The origin of the performance of the BHJs was studied using a combination of physical and optoelectronic characterization methods. X-ray scattering revealed that the domains of 2PDI-nS acceptors are disordered in neat films and in BHJs. The carrier mobility was highest for 2PDI-4S leading to the highest fill factor for the series of acceptors. The open-circuit voltage loss was modeled using two approaches and was found to be low for the series relative to many BHJs. This work demonstrates the utility of fused-sulfur atoms to tune the electron affinity of this class of nonfullerene acceptors.

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