Abstract
To investigate side chain effect of ETVT based photovoltaic polymers, we designed and synthesized the polymers with different solubilizing substituents. The impact of side chains on the solubility, planarity, optical and electronic properties of these ETVT based conjugated polymers was systematically studied. Extending the intrinsic alkyl group or adding new alkyl substituent to the polymer obviously increased the solubility of the resulting polymers. Thus, the polymerization reaction yield was improved to 88% and 81%, for PETVT-TBT24 and PETVT8-TBT, compared to that of 39% for PETVT-TBT. PETVT8-TBT showed blue-shifted absorption spectrum, reduced hole mobility and consequently inferior photovoltaic performance, owing to the steric hindrance caused by redundant octyl group on ETVT unit. However, the introduction of alkyl substitutes in ETVT remarkably increases the open-circuit voltage of PETVT8-TBT based PSCs to 1.03 V, by both decreasing HOMO of the polymer and reducing the energy losses. Extending the intrinsic alkyl group resolved the problem of low solubility of PETVT-TBT, and furthermore, was benefit to improve charge carrier mobility in the resulting polymer based solar cells. As a result, PETVT-TBT24 basically maintained the advantages of ETVT based photovoltaic polymers, realizing a moderate PCE of 7.8% when paired with the non-fullerene acceptor of ITIC.
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