Articles producció científica> Enginyeria Electrònica, Elèctrica i Automàtica

Subphthalocyanine-Diketopyrrolopyrrole Conjugates: 3D Star-Shaped Systems as Non-Fullerene Acceptors in Polymer Solar Cells with High Open-Circuit Voltage

  • Identification data

    Identifier: imarina:9216302
  • Authors:

    Alvaro-Martins, Maria J.
    Sanchez, Jose G.
    Lavarda, Giulia
    Molina, Desire
    Pallares, Josep
    Torres, Tomas
    Marsal, Lluis F.
    Sastre-Santos, Angela
  • Others:

    Author, as appears in the article.: Alvaro-Martins, Maria J.; Sanchez, Jose G.; Lavarda, Giulia; Molina, Desire; Pallares, Josep; Torres, Tomas; Marsal, Lluis F.; Sastre-Santos, Angela;
    Department: Enginyeria Electrònica, Elèctrica i Automàtica
    URV's Author/s: Marsal Garví, Luis Francisco / Pallarès Marzal, Josep / SANCHEZ LÓPEZ, JOSÉ GUADALUPE
    Keywords: Π-systems Subphthalocyanines Performance Organic solar cells Non-fullerene acceptor Interface Hole-transport layer Efficient Diketopyrrolopyrroles Core Boron subphthalocyanines π -systems subphthalocyanines performance organic solar cells non-fullerene acceptor interface infinity-systems efficient core boron subphthalocyanines π -systems
    Abstract: Four star-shaped electron acceptors (C-1-OPh, C-3-OPh, C-1-Cl and C-3-Cl) based on a subphthalocyanine core bearing three diketopyrrolopyrrole wings linked by an acetylene bridge have been synthesized. These derivatives feature two different axial substituents (i. e., 4-tert-butylphenoxy (OPh) or chlorine (Cl)) and for each of them, both the C-1 and the C-3 regioisomers have been investigated. The four compounds exhibit a broad absorption band in the 450-700 nm region, with bandgap values near to 2 eV. These materials were applied in the active layer of inverted bulk-heterojunction polymer solar cells in combination with the donor polymer PBDB-T. Derivatives bearing the OPh axial group showed the best performances, with C-1-OPh being the most promising with a PCE of 3.27 % and a V-oc as high as 1.17 V. Despite presenting the widest absorption range, the photovoltaic results obtained with C-1-Cl turned out to be the lowest (PCE=1.01 %).
    Thematic Areas: Química General chemistry Chemistry, multidisciplinary Chemistry (miscellaneous) Chemistry (all)
    licence for use: https://creativecommons.org/licenses/by/3.0/es/
    Author's mail: lluis.marsal@urv.cat josep.pallares@urv.cat
    Author identifier: 0000-0002-5976-1408 0000-0001-7221-5383
    Record's date: 2024-06-15
    Papper version: info:eu-repo/semantics/publishedVersion
    Link to the original source: https://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/cplu.202100103
    Licence document URL: http://repositori.urv.cat/ca/proteccio-de-dades/
    Papper original source: Chempluschem. 86 (10): 1360-1361
    APA: Alvaro-Martins, Maria J.; Sanchez, Jose G.; Lavarda, Giulia; Molina, Desire; Pallares, Josep; Torres, Tomas; Marsal, Lluis F.; Sastre-Santos, Angela; (2021). Subphthalocyanine-Diketopyrrolopyrrole Conjugates: 3D Star-Shaped Systems as Non-Fullerene Acceptors in Polymer Solar Cells with High Open-Circuit Voltage. Chempluschem, 86(10), 1360-1361. DOI: 10.1002/cplu.202100103
    Article's DOI: 10.1002/cplu.202100103
    Entity: Universitat Rovira i Virgili
    Journal publication year: 2021
    Publication Type: Journal Publications
  • Keywords:

    Chemistry (Miscellaneous),Chemistry, Multidisciplinary
    Π-systems
    Subphthalocyanines
    Performance
    Organic solar cells
    Non-fullerene acceptor
    Interface
    Hole-transport layer
    Efficient
    Diketopyrrolopyrroles
    Core
    Boron subphthalocyanines
    π -systems
    subphthalocyanines
    performance
    organic solar cells
    non-fullerene acceptor
    interface
    infinity-systems
    efficient
    core
    boron subphthalocyanines
    π -systems
    Química
    General chemistry
    Chemistry, multidisciplinary
    Chemistry (miscellaneous)
    Chemistry (all)
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