4.8 Article

Polymerized Small Molecular Acceptor with Branched Side Chains for All Polymer Solar Cells with Efficiency over 16.7%

期刊

ADVANCED MATERIALS
卷 34, 期 14, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.202110155

关键词

all polymer solar cells; branched side chain; efficiency; polymer acceptors; small molecular acceptors

资金

  1. National Natural Science Foundation of China [51825301, 21734001, 52003013]
  2. China Postdoctoral Science Foundation [BX20190023]
  3. Office of Science, Office of Basic Energy Sciences, of the US Department of Energy [DE-AC02-05CH11231]

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This study successfully achieved efficient all-polymer solar cells by designing and synthesizing a series of polymer acceptors. Through the investigation of the structure-property relationship of polymer acceptors, new insights into polymer acceptors were provided, and a feasible approach to develop efficient conjugated polymer acceptors was paved.
The power conversion efficiencies (PCEs) of small molecule acceptor (SMA)-based organic solar cells have already exceeded 18%. However, the development of polymer acceptors still lags far behind their SMA counterparts mainly due to the lack of efficient polymer acceptors. Herein, a series of polymer acceptors named PY-X (with X being the branched alkyl chain) are designed and synthesized by employing the same central core with the SMA L8-BO but with different branched alkyl chains on the pyrrole motif. It is found that the molecular packing of SMA-HD featuring 2-hexyldecyl side chain used in the synthesis of PY-HD is similar to L8-BO, in which the branched alkyl chains lead to condensed and high-order molecular assembly in SMA-HD molecules. When combined with PM6, PY-HD-based all polymer solar cell (all-PSC) exhibits a high PCE of 16.41%, representing the highest efficiency for the binary all-PSCs. Moreover, the side-chain modification on the pyrrole site position further improves the performance of the all-PSCs, and the PY-DT-based device delivers a new record high efficiency of 16.76% (certified as 16.3%). The work provides new insights for understanding the structure-property relationship of polymer acceptors and paves a feasible avenue to develop efficient conjugated polymer acceptors.

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