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Fluorination-enabled optimal morphology leads to over 11% efficiency for inverted small-molecule organic solar cells

Journal Article · · Nature Communications
DOI:https://doi.org/10.1038/ncomms13740· OSTI ID:1623866
 [1];  [2];  [2];  [3];  [2];  [4];  [2];  [2];  [2];  [5];  [4]
  1. National Center for Nanoscience and Technology, Beijing, (China). CAS Key Laboratory of Nanosystem and Hierarchical Fabrication, CAS Center for Excellence in Nanoscience; DOE/OSTI
  2. National Center for Nanoscience and Technology, Beijing, (China). CAS Key Laboratory of Nanosystem and Hierarchical Fabrication, CAS Center for Excellence in Nanoscience
  3. Xi'an Jiaotong Univ., Shaanxi (China). State Key Laboratory for Mechanical Behavior of Materials
  4. National Center for Nanoscience and Technology, Beijing, (China). CAS Key Laboratory of Nanosystem and Hierarchical Fabrication, CAS Center for Excellence in Nanoscience; Univ. of Chinese Academy of Sciences, Beijing (China)
  5. Xi'an Jiaotong Univ., Shaanxi (China). State Key Laboratory for Mechanical Behavior of Materials

Solution-processable small molecules for organic solar cells have attracted intense attention for their advantages of definite molecular structures compared with their polymer counterparts. However, the device efficiencies based on small molecules are still lower than those of polymers, especially for inverted devices, the highest efficiency of which is <9%. Here we report three novel solution-processable small molecules, which contain π-bridges with gradient-decreased electron density and end acceptors substituted with various fluorine atoms (0F, 1F and 2F, respectively). Fluorination leads to an optimal active layer morphology, including an enhanced domain purity, the formation of hierarchical domain size and a directional vertical phase gradation. The optimal morphology balances charge separation and transfer, and facilitates charge collection. As a consequence, fluorinated molecules exhibit excellent inverted device performance, and an average power conversion efficiency of 11.08% is achieved for a two-fluorine atom substituted molecule.

Research Organization:
Lawrence Berkeley National Laboratory (LBNL), Berkeley, CA (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES)
Grant/Contract Number:
AC02-05CH11231
OSTI ID:
1623866
Journal Information:
Nature Communications, Journal Name: Nature Communications Journal Issue: 1 Vol. 7; ISSN 2041-1723
Publisher:
Nature Publishing GroupCopyright Statement
Country of Publication:
United States
Language:
English

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