Cited by 48Organic Electronics and PhotovoltaicsOrganic Light-Emitting Diodes ResearchTiO2 Photocatalysis and Solar Cells

Low band gap copolymers consisting of porphyrins, thiophenes, and 2,1,3‐benzothiadiazole moieties for bulk heterojunction solar cells

Zhou, Weiping, Shen, Ping, Zhao, Bin, Jiang, Peng, Deng, Lijun, Tan, Songting·2011·Journal of Polymer Science Part A: Polymer Chemistry

Abstract

Two novel low band gap conjugated copolymers containing porphyrins, thiophenes, and 2,1,3‐benzothiadiazole (BTZ) moieties were synthesized and applied in bulk heterojunction solar cells. The thermal, optical, electrochemical, and photovoltaic properties of the two copolymers were examined to investigate the effect of the introduction of BTZ moiety in the backbone of the porphyrin polymers. The copolymers exhibited good thermal stability and film‐forming ability. The absorption spectra indicated that the BTZ moiety has significant influence on the UV–visible region spectra of the copolymers: with increasing the molar amount of BTZ moieties in conjugated main chain, the absorption in the range of 450–700 nm is largely broadened and red‐shifted compared to the similar polymers without BTZ moiety, and the optical band gaps of copolymers were narrowed to ∼1.50 eV. The photoluminescence spectra showed that there is effective charge transfer in the whole conjugated main chain. Cyclic voltammetry displayed that the band gaps were reduced effectively by the introduction of the BTZ moieties. The bulk heterojunction solar cells were fabricated based on the blend of the copolymers and [6,6]‐phenyl‐C61‐butyric acid methyl ester (PC61BM) in a 1:2 weight ratio. The maximum power conversion efficiency of 0.91% was obtained by using P2 as the electron donor under the illumination of AM 1.5, 100 mW/cm2. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011

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Crossref · 10.1002/pola.24700

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  • A16 shows a better PCE of 0.91% than A15 due to its high Jsc (from broad and red-shifted absorption in the 450-700 nm range) and Voc (from its lower HOMO levels).

    “A16 shows a better PCE of 0.91% than A15 due to its high J sc (because of broad and redshi  ed absorption in the 450 -700 nm range) and V oc (resulted from its lower HOMO levels). 30”
  • Tan et al. used electron-deficient 2,1,3-benzothiadiazole along with porphyrin to construct two donors A15 and A16.

    “Tan et al. used electron de  cient 2,1,3-benzo-thiadiazole (BT) along with porphyrin to construct two donors A15 and A16 (Fig. 5).”

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Authors
Zhou, W., Shen, P., Zhao, B., Jiang, P., Deng, L., & Tan, S.
Affiliations
Xiangtan University (CN)
Corresponding author
Tan, Songting
Venue
Journal of Polymer Science Part A: Polymer Chemistry
Publisher
Wiley
Published
2011-04-27
Volume
49
Issue
12
Pages
2685-2692
ISSN
  • 0887-624X (ISSN-L)
  • 1099-0518
OpenAlex
W2062782564
Cited by
48
References
0
Citations by year
2023: 1 · 2022: 2 · 2021: 1 · 2020: 2 · 2019: 2 · 2018: 4 · 2017: 6 · 2016: 4 · 2015: 4 · 2014: 7 · 2013: 3 · 2012: 10
FWCI
4.70
Type
journal article
Language
en
Open access
closed
Locations
Journal of Polymer Science Part A Polymer Chemistry (publishedVersion)
Topics
  • Physical Sciences › Engineering › Electrical and Electronic Engineering › Organic Electronics and Photovoltaics
  • Physical Sciences › Engineering › Electrical and Electronic Engineering › Organic Light-Emitting Diodes Research
  • Physical Sciences › Energy › Renewable Energy, Sustainability and the Environment › TiO2 Photocatalysis and Solar Cells
Keywords
thiophene, benzothiadiazole, bulk heterojunction solar cells, organic solar cells, optical band gap narrowing, bathochromic shift, photoluminescence, charge transfer, PC61BM, electron donors, power conversion efficiency

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