4.7 Article

Theoretical Insights into Optoelectronic Properties of Non-Fullerene Acceptors for the Design of Organic Photovoltaics

期刊

ACS APPLIED ENERGY MATERIALS
卷 4, 期 10, 页码 11090-11100

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsaem.1c01994

关键词

organic semiconductors; organic photovoltaics; non-fullerene acceptors; theoretical analysis; density functional theory

资金

  1. Natural Sciences and Engineering Research Council of Canada (NSERC)
  2. Sentinelle Nord (APOGEE)
  3. Centre de recherche sur les materiaux avances (CERMA)

向作者/读者索取更多资源

Organic photovoltaics based on NFAs have attracted great interest in recent years, with fused-ring systems showing promise for various devices. Computational modeling, particularly DFT, is used to predict material properties, but the accuracy of common methods for recent organic semiconductors is still unexplored. Evaluation of DFT functionals and HF theory for common NFAs shows promising results for device optimization.
Organic photovoltaics based on non-fullerene acceptors (NFAs) have gained enormous interest over the past few years. Recent fused-ring systems such as ITIC, IDT, and Y families are particularly promising for several photovoltaic devices. Since the complexity of these molecular designs has grown substantially, the development of materials with specific properties has become a laborious process. Therefore, many studies employ computational modeling, in particular density functional theory (DFT), to anticipate material electronic properties. Such approaches provide useful information about proposed organic semiconductors, such as optical absorption, frontier orbital energy levels, and molecular geometries. However, the accuracy of the common methods for recent organic semiconductors has not been explored. Thus, we herein evaluate a series of DFT functionals and Hartree-Fock (HF) theory for a collection of 14 common NFAs. Computational results are compared with physical properties from cyclic voltammetry, photoelectron spectroscopy, UV-visible absorption spectroscopy, and ellipsometry. By applying empirical corrections from linear fits, mean absolute errors between theoretical and experimental results below 0.05 eV could be achieved for the highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) energies as well as maximum absorption energies. Moreover, all of these experimental results for these 14 common NFAs could be useful for future device optimization.

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