We report transient photoinduced absorption (t-PA) and magnetic field ( B)-dependent t-PA (t-MPA( B)) in a pristine low band gap π-conjugated copolymer composed of donor and acceptor moieties, namely, the poly[[4,8-bis[(2-ethylhexyl)oxy]benzo[1,2-b:4,5-b']dithiophene-2,6-diyl][3-fluoro-2-[(2-ethylhexyl)carbonyl]thi-eno[3,4- b]thiophenediyl]]) (or PTB7) used in photovoltaic applications. Unlike traditional π-conjugated polymers in which the primary photoexcitations are singlet excitons (SE), in pristine PTB7 we find at short times coexistence of two primary photoexcitation species, namely, SE and triplet-triplet (TT) pair. Both species are photogenerated directly from the ground state and are spin-correlated.
View Article and Find Full Text PDFWe have utilized a plethora of transient and steady state optical and magneto-optical spectroscopies in a broad spectral range (0.25-2.5 eV) for elucidating the primary and long-lived photoexcitations in a low band-gap π-conjugated donor-acceptor (DA) copolymer used for efficient photovoltaic solar cells.
View Article and Find Full Text PDFRecently, much effort has been devoted to improve the efficiency of organic photovoltaic solar cells based on blends of donors and acceptors molecules in bulk heterojunction architecture. One of the major losses in organic photovoltaic devices has been recombination of polaron pairs at the donor-acceptor domain interfaces. Here, we present a novel method to suppress polaron pair recombination at the donor-acceptor domain interfaces and thus improve the organic photovoltaic solar cell efficiency, by doping the device active layer with spin 1/2 radical galvinoxyl.
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