Toluene Processed All‐Polymer Solar Cells with 18% Efficiency and Enhanced Stability Enabled by Solid Additive: Comparison Between Sequential‐Processing and Blend‐Casting

Author:

Zhang Guoping1,Zhao Chaoyue12,Zhu Liangxiang1,Wang Lihong1,Xiong Wenzhao3,Hu Huawei3,Bai Qing1,Wang Yaping1,Xie Chen1,You Peng1,Yan He2,Wu Dan1,Yang Tao4,Qiu Mingxia1,Li Shunpu1,Zhang Guangye1ORCID

Affiliation:

1. College of New Materials and New Energies Shenzhen Technology University Shenzhen 518118 China

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

3. State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, Center for Advanced Low‐dimension Materials, College of Materials Science and Engineering Donghua University Shanghai 201620 China

4. Julong College Shenzhen Technology University Shenzhen 518118 China

Abstract

The emergence of polymerized small molecule acceptors (PSMAs) has significantly improved the performance of all‐polymer solar cells (all‐PSCs). However, the pace of device engineering lacks behind that of materials development, so that a majority of the PSMAs have not fulfilled their potentials. Furthermore, most high‐performance all‐PSCs rely on the use of chloroform as the processing solvent. For instance, the recent high‐performance PSMA, named PJ1‐γ, with high LUMO, and HOMO levels, could only achieve a PCE of 16.1% with a high‐energy‐level donor (JD40) using chloroform. Herein, we present a methodology combining sequential processing (SqP) with the addition of 0.5%wt PC71BM as a solid additive (SA) to achieve an impressive efficiency of 18.0% for all‐PSCs processed from toluene, an aromatic hydrocarbon solvent. Compared to the conventional blend‐casting (BC) method whose best efficiency (16.7%) could only be achieved using chloroform, the SqP method significantly boosted the device efficiency using toluene as the processing solvent. In addition, the donor we employ is the classic PM6 that has deeper energy levels than JD40, which provides low energy loss for the device. We compare the results with another PSMA (PYF‐T‐o) with the same method. Finally, an improved photostability of the SqP devices with the incorporation of SA is demonstrated.

Funder

Fundamental Research Funds for the Central Universities

National Natural Science Foundation of China

Publisher

Wiley

Subject

Energy (miscellaneous),Waste Management and Disposal,Environmental Science (miscellaneous),Water Science and Technology,General Materials Science,Renewable Energy, Sustainability and the Environment

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