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Double Linker Triphenylamine Dyes for Dye-Sensitized Solar Cells

Author

Listed:
  • Peter J. Holliman

    (College of Engineering, Bay Campus, Swansea University, Swansea SA1 8EN, UK)

  • Moneer Mohsen

    (Ministry of Science and Technology, Materials Research Directorate, Baghdad, Iraq)

  • Arthur Connell

    (College of Engineering, Bay Campus, Swansea University, Swansea SA1 8EN, UK)

  • Christopher P. Kershaw

    (College of Engineering, Bay Campus, Swansea University, Swansea SA1 8EN, UK)

  • Diana Meza-Rojas

    (College of Engineering, Bay Campus, Swansea University, Swansea SA1 8EN, UK)

  • Eurig W. Jones

    (College of Engineering, Bay Campus, Swansea University, Swansea SA1 8EN, UK)

  • Dawn Geatches

    (Scientific Computing Department, STFC Daresbury Laboratory, Daresbury, Warrington WA4 4AD, UK)

  • Kakali Sen

    (Scientific Computing Department, STFC Daresbury Laboratory, Daresbury, Warrington WA4 4AD, UK)

  • Ya-Wen Hsiao

    (Scientific Computing Department, STFC Daresbury Laboratory, Daresbury, Warrington WA4 4AD, UK)

Abstract

Most organic dyes synthesized for dye-sensitized solar cells (DSC) use a single linker group to bind to the metal oxide photo-anode. Here we describe the synthesis and testing of two new triphenylamine dyes containing either two carboxylic acids 5-[2-(4-diphenylamino-phenyl)-vinyl]-isophthalic acid ( 10 ) or two cyanoacrylic acids (2Z, 2′Z)-3, 3′-(5-((E)-4-(diphenylamino) styryl)-1, 3-phenylene) bis (2-cyanoacrylic acid) ( 8 ) as linker groups. Full characterization data are reported for these dyes and their synthetic intermediates. DSC devices have been prepared from these new dyes either by passive or fast dyeing and the dyes have also been tested in co-sensitized DSC devices leading to a PCE (η = 5.4%) for the double cyanoacrylate linker dye ( 8 ) co-sensitized with D149. The dye:TiO 2 surface interactions and dye excitations are interpreted using three modelling methods: density functional theory (at 0 K); molecular dynamics (at 298 K); time dependent density functional theory. The modelling results show the preferred orientation of both dyes on an anatase (1 0 1) TiO 2 surface to be horizontal, and both the simulated and experimental absorption spectra of the dye molecules indicate a red shifted band for ( 8 ) compared to ( 10 ). This is in line with broader light harvesting and J sc for ( 8 ) compared to ( 10 ).

Suggested Citation

  • Peter J. Holliman & Moneer Mohsen & Arthur Connell & Christopher P. Kershaw & Diana Meza-Rojas & Eurig W. Jones & Dawn Geatches & Kakali Sen & Ya-Wen Hsiao, 2020. "Double Linker Triphenylamine Dyes for Dye-Sensitized Solar Cells," Energies, MDPI, vol. 13(18), pages 1-16, September.
  • Handle: RePEc:gam:jeners:v:13:y:2020:i:18:p:4637-:d:409861
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    Citations

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    Cited by:

    1. Vasileios Kapsalis & Grigorios Kyriakopoulos & Miltiadis Zamparas & Athanasios Tolis, 2021. "Investigation of the Photon to Charge Conversion and Its Implication on Photovoltaic Cell Efficient Operation," Energies, MDPI, vol. 14(11), pages 1-16, May.
    2. Carmen Coppola & Maria Laura Parisi & Adalgisa Sinicropi, 2023. "The Role of Organic Compounds in Dye-Sensitized and Perovskite Solar Cells," Energies, MDPI, vol. 16(2), pages 1-4, January.

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