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Structure-Property Relationships for the Electronic Applications of Bis-Adduct Isomers of Phenyl-C61 Butyric Acid Methyl Ester.
Hou, Xueyan; Coker, Jack F; Yan, Jun; Shi, Xingyuan; Azzouzi, Mohammed; Eisner, Flurin D; McGettrick, James D; Tuladhar, Sachetan M; Abrahams, Isaac; Frost, Jarvist M; Li, Zhe; Dennis, T John S; Nelson, Jenny.
Afiliación
  • Hou X; Department of Physics, Imperial College London, London SW7 2AZ, U.K.
  • Coker JF; School of Physical and Chemical Sciences, Queen Mary University of London, London E1 4NS, U.K.
  • Yan J; Department of Physics, Imperial College London, London SW7 2AZ, U.K.
  • Shi X; Department of Physics, Imperial College London, London SW7 2AZ, U.K.
  • Azzouzi M; School of Science and Engineering, The Chinese University of Hong Kong, Shenzhen, Guangdong Province 518172, P. R. China.
  • Eisner FD; Department of Physics, Imperial College London, London SW7 2AZ, U.K.
  • McGettrick JD; Department of Physics, Imperial College London, London SW7 2AZ, U.K.
  • Tuladhar SM; Department of Physics, Imperial College London, London SW7 2AZ, U.K.
  • Abrahams I; SPECIFIC, Swansea University Bay Campus, Swansea, Wales SA1 8EN, U.K.
  • Frost JM; Department of Physics, Imperial College London, London SW7 2AZ, U.K.
  • Li Z; School of Physical and Chemical Sciences, Queen Mary University of London, London E1 4NS, U.K.
  • Dennis TJS; Department of Physics, Imperial College London, London SW7 2AZ, U.K.
  • Nelson J; School of Engineering and Materials Sciences, Queen Mary University of London, London E1 4NS, U.K.
Chem Mater ; 36(1): 425-438, 2024 Jan 09.
Article en En | MEDLINE | ID: mdl-38222935
ABSTRACT
Higher adducts of a fullerene, such as the bis-adduct of PCBM (bis-PCBM), can be used to achieve shallower molecular orbital energy levels than, for example, PCBM or C60. Substituting the bis-adduct for the parent fullerene is useful to increase the open-circuit voltage of organic solar cells or achieve better energy alignment as electron transport layers in, for example, perovskite solar cells. However, bis-PCBM is usually synthesized as a mixture of structural isomers, which can lead to both energetic and morphological disorder, negatively affecting device performance. Here, we present a comprehensive study on the molecular properties of 19 pure bis-isomers of PCBM using a variety of characterization methods, including ultraviolet photoelectron spectroscopy, thermal gravimetric analysis, differential scanning calorimetry, single crystal structure, and (time-dependent) density functional theory calculation. We find that the lowest unoccupied molecular orbital of such bis-isomers can be tuned to be up to 170 meV shallower than PCBM and up to 100 meV shallower than the mixture of unseparated isomers. The isolated bis-isomers also show an electron mobility in organic field-effect transistors of up to 4.5 × 10-2 cm2/(V s), which is an order of magnitude higher than that of the mixture of bis-isomers. These properties enable the fabrication of the highest performing bis-PCBM organic solar cell to date, with the best device showing a power conversion efficiency of 7.2%. Interestingly, we find that the crystallinity of bis-isomers correlates negatively with electron mobility and organic solar cell device performance, which we relate to their molecular symmetry, with a lower symmetry leading to more amorphous bis-isomers, less energetic disorder, and higher dimensional electron transport. This work demonstrates the potential of side chain engineering for optimizing the performance of fullerene-based organic electronic devices.

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Chem Mater Año: 2024 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Chem Mater Año: 2024 Tipo del documento: Article País de afiliación: Reino Unido