Tuning the synthesis of fully conjugated block copolymers to minimize architectural heterogeneityElectronic supplementary information (ESI) available: NMR analysis of block copolymers, details of model reaction, GPC analysis of mixture of homopolymers, and RSoXS data of block copolymers. See DOI: 10.1039/c7ta06758e

• Main Authors: Lee, Youngmin, Aplan, Melissa P, Seibers, Zach D, Kilbey, S. Michael, Wang, Qing, Gomez, Enrique D
• Format: Article
• Language: English
• ISSN: 2050-7488; 2050-7496
• DOI: 10.1039/c7ta06758e

Conjugated block copolymers simultaneously control the mesoscale morphology and interfacial structure of the active layer in organic electronic devices. Fully conjugated block copolymers, where both backbones are conjugated, are commonly synthesized in two steps. First, poly(3-alkylthiophene-2,5-diyl) (P3HT) is synthesized by Kumada catalyst transfer/Grignard metathesis polymerization. The second block, typically a push-pull alternating copolymer, is added on to the P3HT macroreagent in a chain-extension reaction using either a Suzuki or a Stille polycondensation. Consequently, products can be a mixture of homopolymers, diblock copolymers, and multi-block copolymers. We demonstrate the optimum reaction conditions for the two-step synthesis of poly(3-hexylthiophene-2,5-diyl)- block -poly((9,9-bis-(2-octyl)fluorene-2,7-diyl)- alt -(4,7-di(thiophene-2-yl)-2,1,3-benzothiadiazole)-5′,5′′-diyl) (P3HT- b -PFTBT), a block copolymer that can be used as the sole active-layer material in organic photovoltaic devices. In the first reaction, preventing excess Grignard reagent to avert excess in the stoichiometry between Grignard reagent and monomer ensures end-group control of the P3HT macroreagent. In the second reaction, asymmetric monomer feed ratios with excess fluorene promotes coupling of PFTBT to P3HT. Using P3HT- b -PFTBT as an example, we demonstrate the synthetic parameters that are important to produce diblock copolymers with minimal impurities. This, in turn, promotes microphase separation in block copolymer films and leads to enhanced power conversion efficiencies in block copolymer solar cell devices. Control of conversion, end group composition, and feed ratio is crucial to minimize homopolymer impurities in the synthesis of conjugated block copolymers for photovoltaics.