Journal
ENERGY & ENVIRONMENTAL SCIENCE
Volume 16, Issue 12, Pages 5863-5870Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d3ee02700g
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A new alternating copolymer donor was designed for all-polymer solar cells, and the addition of a small-molecule acceptor improved the power conversion efficiency and blend morphology.
Organic photovoltaic cells based on disordered materials suffer significant energy losses that limit the power conversion efficiencies (PCEs). For all-polymer solar cells (all-PSCs), the complicated blend morphology caused by the high probability of chain entanglement will exacerbate this situation. Here, we designed an alternating copolymer donor, PDBQx-TCl, based on dithieno[2,3-d:2 ',3 '-d ']benzo[1,2-b:4,5-b ']dithiophene and dithieno[3,2-f:2 ',3 '-h]quinoxaline units and studied its application in all-PSCs. By blending with the polymer acceptor PY-IT, the device obtained a moderate PCE of 16.8%. We then incorporated a small-molecule acceptor, BTA3-4F, into the PDBQx-TCl:PY-IT blend, which not only tuned the optical absorption and aligned energy levels but also suppressed the energy disorder by optimizing the blend morphology. As a result, the ternary device recorded an outstanding PCE of 18.6%, which is much higher than the binary all-PSC. This work demonstrates that suppressing energy disorder by adding small molecules into binary all-PSCs is a feasible approach to improve photovoltaic performance. The energy disorder of binary all-PSCs based on PDBQx-TCl and PY-IT is suppressed by adding a new small molecule (BTA3-4F), leading to an impressive power conversion efficiency of 18.6%.
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