Excitation Dynamics in Low Band Gap Donor-Acceptor Copolymers and Blends

Donor–acceptor (D–A) type copolymers show great potential for the application in the active layer of organic solar cells. Nevertheless the nature of the excited states, the coupling mechanism and the relaxation pathways following photoexcitation are yet to be clarified. We carried out comparative measurements of the steady state absorption and photoluminescence (PL) on the copolymer poly[N‐(1‐octylnonyl)‐2,7‐carbazole]‐alt‐5,5‐[4′,7′‐di(thien‐2‐yl)‐2′,1′,3′‐benzothiadiazole] (PCDTBT), its building blocks as well as on the newly synthesized N‐(1‐octylnonyl)‐2,7‐bis‐[(5‐phenyl)thien‐2‐yl)carbazole (BPT‐carbazole). The high‐energy absorption band (HEB) of PCDTBT was identified with absorption of carbazoles with adjacent thiophene rings while the low‐energy band (LEB) originates instead from the charge transfer (CT) state delocalized over the aforementioned unit with adjacent benzothiadiazole group. Photoexcitation of the HEB is followed by internal relaxation prior the radiative decay to the ground state. Adding PC70BM results in the efficient PL quenching within the first 50 ps after excitation. From the PL excitation experiments no evidence for a direct electron transfer from the HEB of PCDTBT towards the fullerene acceptor was found, therefore the internal relaxation mechanisms within PCDTBT can be assumed to precede. Our findings indicate that effective coupling between copolymer building blocks governs the photovoltaic performance of the blends. The excitation dynamics in donor‐acceptor copolymer PCDTBT are analyzed using comparative absorption and PL measurements of the polymer and its building blocks as well as a time‐resolved PL study of neat copolymer and blend films. The results indicate that the effective coupling between copolymer building blocks governs the photovoltaic performance of the blends.