Optimizing Double‐Fibril Network Morphology via Solid Additive Strategy Enables Binary All‐Polymer Solar Cells with 19.50% Efficiency

Author:

Song Jiali12,Li Chao3,Ma Haisheng2,Han Bingyu4,Wang Qianqian5,Wang Xunchang6,Wei Donghui5,Bu Laju4,Yang Renqiang6,Yan He3,Sun Yanming12ORCID

Affiliation:

1. Hangzhou International Innovation Institute Beihang University Hangzhou 311115 P. R. China

2. School of Chemistry Beihang University Beijing 100191 P. R. China

3. Department of Chemistry and Hong Kong Branch of Chinese National Engineering Research Center for Tissue Restoration and Reconstruction Hong Kong University of Science and Technology Clear Water Bay Kowloon Hong Kong 999077 P. R. China

4. School of Chemistry Xi'an Jiaotong University Xi'an Shaanxi 710049 P. R. China

5. College of Chemistry Zhengzhou University Zhengzhou Henan 450001 P. R. China

6. Key Laboratory of Optoelectronic Chemical Materials and Devices (Ministry of Education) School of Optoelectronic Materials & Technology Jianghan University Wuhan 430056 P. R. China

Abstract

AbstractDouble‐fibril network morphology (DFNM), in which the donor and the acceptor can self‐assemble into a double‐fibril structure, is beneficial for exciton dissociation and charge transport in organic solar cells. Herein, it is demonstrated that such DFNM can be constructed and optimized in all‐polymer solar cells (all‐PSCs) with the assistance of 2‐alkoxynaphthalene volatile solid additives. It is revealed that the incorporation of 2‐alkoxynaphthalene can induce a stepwise regulation in the aggregation of donor and acceptor molecules during film casting and thermal annealing processes. Through altering the alkoxy of 2‐alkoxynaphthalene solid additives, both the intermolecular interactions and molecular miscibility with the host materials can be precisely tuned, which allows for the optimization of the molecular aggregation process and facilitation of molecular self‐assembly, and thus leading to reinforced molecular packing and optimized DFNM. As a result, an unprecedented efficiency of 19.50% (certified as 19.1%) is obtained for 2‐ethoxynaphthalene‐processed PM6:PY‐DT‐X all‐PSCs with excellent photostability (T80 = 1750 h). This work reveals that the optimization of DFNM via solid additive strategy is a promising avenue to boosting the performance of all‐PSCs.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Beijing Municipality

National Key Research and Development Program of China

Shenzhen Fundamental Research Program

Innovation and Technology Commission

Publisher

Wiley

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