4.8 Article

Nonconjugated Terpolymer Acceptors with Two Different Fused-Ring Electron-Deficient Building Blocks for Efficient All-Polymer Solar Cells

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 13, Issue 5, Pages 6442-6449

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.0c17722

Keywords

all polymer solar cells; copolymer; nonconjugated polymer acceptor; power conversion efficiency; terpolymer

Funding

  1. Swedish Research Council [2015-04853, 2016-06146, 2019-04683]
  2. Swedish Research Council Formas
  3. Knut and Alice Wallenberg Foundation [2017.0186, 2016.0059]
  4. Swedish Energy Council [48598-1]
  5. China Postdoctoral Science Foundation [2020M673054]
  6. Postdoctoral Fund of Jinan University
  7. National Natural Science Foundation of China [22005121]
  8. NSFC [61774077]
  9. Sino-Danish Centre for Education and Research
  10. Open Fund of the State Key Laboratory of Luminescent Materials and Devices (South China University of Technology) [2020-skllmd-07]
  11. Vinnova [2019-04683] Funding Source: Vinnova
  12. Swedish Research Council [2015-04853, 2019-04683] Funding Source: Swedish Research Council

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The study developed a series of low band gap nonconjugated terpolymer acceptors using a ternary polymerization strategy, incorporating ITIC building blocks to optimize the photoelectric properties and enhance the performance of all-polymer solar cells.
The ternary polymerization strategy of incorporating different donor and acceptor units forming terpolymers as photovoltaic materials has been proven advantageous in improving power conversion efficiencies (PCEs) of polymer solar cells (PSCs). Herein, a series of low band gap nonconjugated terpolymer acceptors based on two different fused-ring electron-deficient building blocks (IDIC16 and ITIC) with adjustable photoelectric properties were developed. As the third component, ITIC building blocks with a larger pi-conjugation structure, shorter solubilizing side chains, and red-shifted absorption spectrum were incorporated into an IDIC16-based nonconjugated copolymer acceptor PF1-TS4, which built up the terpolymers with two conjugated building blocks linked by flexible thioalkyl chain-thiophene segments. With the increasing ITIC content, terpolymers show gradually broadened absorption spectra and slightly down-shifted lowest unoccupied molecular orbital levels. The active layer based on terpolymer PF1-TS4-60 with a 60% ITIC unit presents more balanced hole and electron mobilities, higher photoluminescence quenching efficiency, and improved morphology compared to those based on PF1-TS4. In all-polymer solar cells (all-PSCs), PF1-TS4-60, matched with a wide band gap polymer donor PM6, achieved a similar open-circuit voltage (V-oc) of 0.99 V, a dramatically increased short-circuit current density (J(sc)) of 15.30 mA cm(-2), and fill factor (FF) of 61.4% compared to PF1-TS4 = 0.99 V, J(sc) = 11.21 mA cm(-2), and FF = 55.6%). As a result, the PF1-TS4-60-based all-PSCs achieved a PCE of 9.31%, which is similar to 50% higher than the PF1-TS4-based ones (6.17%). The results demonstrate a promising approach to develop high-performance nonconjugated terpolymer acceptors for efficient all-PSCs by means of ternary polymerization using two different A-D-A-structured fused-ring electron-deficient building blocks.

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