The influence of conjugated polymer side chain manipulation on the efficiency and stability of polymer solar cells

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Abstract

The stability of polymer solar cells (PSCs) can be influenced by the introduction of particular moieties on the conjugated polymer side chains. In this study, two series of donor-acceptor copolymers, based on bis(thienyl)dialkoxybenzene donor and benzo[c][1,2,5]thiadiazole (BT) or thiazolo[5,4-d]thiazole (TzTz) acceptor units, were selected toward effective device scalability by roll-coating. The influence of the partial exchange (5% or 10%) of the solubilizing 2-hexyldecyloxy by alternative 2-phenylethoxy groups on efficiency and stability was investigated. With an increasing 2-phenylethoxy ratio, a decrease in solar cell efficiency was observed for the BT-based series, whereas the efficiencies for the devices based on the TzTz polymers remained approximately the same. The photochemical degradation rate for PSCs based on the TzTz polymers decreased with an increasing 2-phenylethoxy ratio. Lifetime studies under constant sun irradiance showed a diminishing initial degradation rate for the BT-based devices upon including the alternative side chains, whereas the (more stable) TzTz-based devices degraded at a faster rate from the start of the experiment upon partly exchanging the side chains. No clear trends in the degradation behavior, linked to the copolymer structural changes, could be established at this point, evidencing the complex interplay of events determining PSCs' lifetime.

Figures

  • Figure 1. Chemical structures of a few low bandgap copolymer organic photovoltaics (OPV) reference materials [14–16]. PTB7-th, poly{4,8-bis[5-(2-ethylhexyl)thiophen-2-yl]benzo[1,2-b:4,5-b1]dithiophene2,6-diyl-alt-3-fluoro-2-[(2-ethylhexyl)carbonyl]thieno[3,4-b]thiophene-4,6-diyl}.
  • Figure 2. Chemical structures of the investigated statistical copolymers P3a,b and P4a,b.
  • Table 1. Molecular, optical and electrochemical properties of the synthesized polymers.
  • Figure  3. Normalized UV‐VIS  absorption  spectra  for  the  benzo[c][1,2,5]thiadiazole  (BT)‐  (a)  and  thiazolo[5,4‐d]thiazole (TzTz)‐ (b) based polymer series. 
  • Table 2. Current-voltage (IV) parameters 1 (Voc, Jsc, fill factor (FF) and power conversion efficiency (PCE)) for the polymer:phenyl-C61-butyric acid methyl ester (PC61BM) RC and SC solar cells based on P1, P2, P3a, P3b, P4a and P4b.
  • Figure 4. Maximum values of the normalized UV-VIS absorption of the polymer films as a function of time during sun irradiance (a,d), average lifetime measurements (ISOS-L-1 [35]) of the polymer solar cells (PSCs) normalized in terms of PCE (b,e) and the thermal degradation test (ISOS-D-2 [35]) of the PSCs normalized in terms of PCE (c,f) for the BT- (a–c) and TzTz- (d–f) based polymer series.
  • Figure 5. Optical microscope images (50ˆ magnification) of the active layers of RC PSCs based on P1 (a), P3a (b) and P3b (c) after exposure to 85 ˝C for 0 h (1), 5 h (2), 24 h (3) and four days (4).
  • Figure 6. ptical icroscope i ages ( ith 50ˆ agnification) of the active layers of RC PSCs based on P2 (a), P4a (b) and P4b (c) after exposure to 85 ˝C for zero days (1) and seven days (2).

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APA

Heckler, I. M., Kesters, J., Defour, M., Madsen, M. V., Penxten, H., D’Haen, J., … Bundgaard, E. (2016). The influence of conjugated polymer side chain manipulation on the efficiency and stability of polymer solar cells. Materials, 9(3). https://doi.org/10.3390/ma9030181

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