4.6 Article

p-nitrophenol-terminated alkyl side chain substituted polymer as high dielectric constant polymer additive enables efficient organic solar cells

Journal

OPTICAL MATERIALS
Volume 127, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.optmat.2022.112347

Keywords

p-Nitrophenol; Side chain engineering; Dielectric constant; Polymer additive; Polymer solar cell

Funding

  1. Industrial Guidance Project for Colleges and Universities of Gansu Province [2020C-07]
  2. National Nature Science Foundation of China [51903112, 62164007]
  3. Lanzhou Jiaotong University-Tianjin University Joint Innovation Fund [2019057]

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In this study, a high dielectric constant polymer PBTA-NO2 was synthesized by introducing p-nitrophenol-terminated alkyl side chain into the benzotriazole unit. PBTA-NO2 exhibited similar absorption spectra, lower energy levels, stronger aggregation characteristics, and higher dielectric constant compared to the controlled polymer PBTA-C10H21. Furthermore, when PBTA-NO2 was used as an additive in the active layer of PM6:Y6 based polymer solar cells, the power conversion efficiency was increased by 6% due to improved exciton dissociation and carrier transport.
Herein, we introduced p-nitrophenol-terminated alkyl side chain into the benzotriazole unit and synthesized a high dielectric constant polymer PBTA-NO2 (epsilon(r) = 7.1). The properties as absorption spectra, energy levels, aggregation, dielectric constant, photovoltaic performance, etc. of PBTA-NO2 were analyzed and compared with its controlled polymer PBTA-C10H21. It is found that the PBTA-NO2 exhibits a similar absorption spectrum, lower highest occupied molecular orbital (HOMO) energy level, stronger aggregation characteristic and higher dielectric constant at 1 kHz in contrast to that of PBTA-C10H21. Beyond that, the PBTA-NO2 was adopted as a high dielectric constant polymer additive into the active layer of the PM6:Y6 based polymer solar cells (PSCs). The incorporation of 5 wt% PBTA-NO2 slightly increased the relative dielectric constant (epsilon(r)) of the blend film from 4.4 to 4.8 and simultaneously improved the morphology of the active layer, which promoted the exciton dissociation and carrier transport, inhibited bimolecular recombination, and eventually increased the power conversion efficiency (PCE) by 6% as compared to the original device.

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