4.8 Article

15.71% Efficiency All-Small-Molecule Organic Solar Cells Based on Low-Cost Synthesized Donor Molecules

Journal

ADVANCED FUNCTIONAL MATERIALS
Volume 32, Issue 13, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.202110159

Keywords

all small-molecule organic solar cells; fluorine substitution; low synthetic cost; side chain engineering; small-molecule donor materials

Funding

  1. National Key Research and Development Program of China [2019YFA0705900]
  2. MOST
  3. National Natural Science Foundation of China [51820105003, 21734008, 61904181]
  4. Basic and Applied Basic Research Major Program of Guangdong Province [2019B030302007]

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This study focuses on the key issues of low cost, high efficiency, and high stability in organic solar cells (OSCs). By designing and synthesizing two new low-cost small-molecule donors and investigating the chemical steric effect on the photophysical properties, charge transfer, and photovoltaic properties, the research has achieved a superior power conversion efficiency of 15.71% and demonstrated excellent potential for future commercial applications.
Low cost, high efficiency, and high stability are the three key issues of organic solar cells (OSCs) that should be carefully considered to meet the requirement of future commercial applications. Therefore, the development of high-performance organic photovoltaic materials with low synthetic cost has been becoming a crucial challenge in the field of OSCs. Herein, two new low-cost small-molecule donors (SM-BF1 and SM-BF2) are designed and synthesized with a facile synthetic route by replacing 4-bromo-2-fluorobenzenethiol and 4-bromo-3-fluorobenzenethiol with low-cost 4-bromo-2-fluoro-1-iodobenzene and 4-bromo-3-fluoro-1-iodobenzene as key raw materials. Besides, the influence of the chemical steric effect of the phenyl conjugated side chains of the benzodithiophene (BDT) unit on photophysical properties, charge transfer, and photovoltaic properties are deeply investigated by the modulation of fluorine atom substituted position. As a result, SM-BF1 with ortho-fluorinated substituent has outstanding crystallization properties and better miscibility with acceptor Y6 and exhibits more desirable morphology and more balanced charge-carrier transport properties, leading to a superior power conversion efficiency (PCE) to 15.71%. More encouragingly, according to the figure of merit (FOM) and the industrial figure of merit (i-FOM) to evaluate the small-molecule donors, the SM-BF1-based device has excellent potential for future commercial applications.

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