4.7 Article

Synergy strategy to the flexible alkyl and chloride side-chain engineered quinoxaline-based D-A conjugated polymers for efficient non-fullerene polymer solar cells

Journal

MATERIALS CHEMISTRY FRONTIERS
Volume 5, Issue 4, Pages 1906-1916

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0qm00826e

Keywords

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Funding

  1. National Science Foundation of China [51573154, 51673031]
  2. Natural Science Foundation of the Jiangsu Higher Institutions of China [18KJA480001]
  3. Natural Science Foundation of Jiangsu Province [BK20141151]
  4. Jiangsu Provincial Talents Project of High-Level Innovation and Entrepreneurship
  5. Talent Project of Jiangsu Specially - Appointed Professor

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By developing two medium band-gap (MBG) donor-acceptor (D-A) copolymers, combining chlorine atoms and flexible side-chain engineered quinoxaline (Qx) as the acceptor unit, and based on alkylthio-thienyl substituted benzodithiophene (BDTTS) donor unit, the photovoltaic performance of NF-PSCs can be significantly improved. The incorporation of chlorination and suitable flexible side-chains can lead to higher V-OC, enhancing J(SC) and FF parameters, resulting in an increase in power conversion efficiency (PCE) to 12.59% compared to 11.10%.
With the meteoric progress on acceptor materials for non-fullerene polymer solar cells (NF-PSCs), exploring efficient and matched copolymer donor materials has become a key issue. Herein, to achieve a balance among open-circuit voltage (V-OC), short-circuit current density (J(SC)) and fill factor (FF), we have developed two medium band-gap (MBG) donor-acceptor (D-A) copolymers, namely, PBDTTS-TClQx and PBDTTS-TClSQx, by combining chlorine atoms and flexible alkyl (R) or alkylthio (SR) side-chains engineered quinoxaline (Qx) as the acceptor unit, as well as based on a well-known alkylthio-thienyl substituted benzodithiophene (BDTTS) donor unit. These copolymers were successfully synthesized and finally facilely employed as photovoltaic donor materials for NF-PSCs. After blending with the MeIC acceptor, the PBDTTS-TClQx:MeIC blend film exhibited more balanced electron/hole mobility (mu(h)/mu(e)), better efficient exciton dissociation and nice morphology in comparison with the PBDTTS-TClSQx:MeIC blend film. Encouragingly, chlorination and appropriate side-chains engineering Qx can result in a higher V-OC, thus leading to enhancement in J(SC) and FF parameters. More excitingly, the PBDTTS-TClQx:MeIC-based PSCs exhibit a higher power conversion efficiency (PCE) of 12.59% higher than that of the device based on the PBDTTS-TClSQx:MeIC blend that had a PCE of 11.10%. The higher performance arises from the enhancement in current density (J(SC)) of 17.07 mA cm(-2) and fill factor (FF) of 77.2%. The impressive FF of up to 77.2% is the highest reported for Qx-type copolymers-based NF solar cells to date. These results disclose that chlorination and suitable flexible side-chains are promising strategies to improve the photovoltaic performance of copolymers.

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