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In Situ Characterization of Polymer–Fullerene Bilayer Stability

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journal contribution
posted on 27.01.2015, 00:00 by Deborah Leman, Mary Allison Kelly, Stuart Ness, Sebastian Engmann, Andrew Herzing, Chad Snyder, Hyun Wook Ro, R. Joseph Kline, Dean M. DeLongchamp, Lee J. Richter
A consensus is emerging that mixed phases are present in bulk heterojunction organic photovoltaic (OPV) devices. Significant insights into the mixed phases have come from bilayer stability measurements, in which an initial sample consisting of material pure layers of donor and acceptor is thermally treated, resulting in swelling of one layer by the other. We present a comparative study of the stability of polymer/fullerene bilayers using two common OPV polymer donors poly­(3-hexylthiophene), P3HT, and poly­[N-9′-heptadecanyl-2,7-carbazole-alt-5,5-(4′,7′-di-2-thienyl-2′,1′,3′-benzothiadiazole)], PCDTBT, and four fullerene acceptors phenyl-C61-butyric acid methyl ester, phenyl-C71-butyric acid methyl ester, [60]­PCBM bis-adduct, and indene C60 bis-adduct. Using in situ spectroscopic ellipsometry to characterize the quasi-steady state behavior of the films, we find that the polymer glass transition temperature (Tg) is critical to the bilayer stability, with no significant changes occurring below Tg of the high Tg PCDTBT. Above the polymer Tg, we find the behavior is irreversible and most consistent with swelling of the polymer by the fullerene, constrained by tie chains in the polymer network and influenced by the rubbery dynamics of the mixed region. The swelling varies significantly with the nature of the fullerene and the polymer. Across the eight systems studied, there is no clear relationship between swelling and OPV device performance. The relationship between the observed swelling and the underlying fullerene–polymer miscibility is explored via Flory–Rehner theory.