19.35% Efficient Binary Bulk‐Heterojunction Organic Photovoltaic Enabled by Optimizing Bromine‐Substituted Self‐Assembled Carbazole Based Molecules

Author:

Sun Xiaokang12,Zhang Chenyang34,Yao Yiguo3,Lv Jie156,Yao Jie1,Ding Xiaoman1,Lu Manjia1,Zhu Liangxiang7,Zhang Guangye7,Lin Haoran1,Shi Yumeng8,Wang Kai34,Yang Chunming9,Ouyang Xiaoping2,Hu Hanlin1,McCulloch Iain1011,Lin Yuanbao1112ORCID

Affiliation:

1. Hoffmann Institute of Advanced Materials Shenzhen Polytechnic University 7098 Liuxian Boulevard Shenzhen 518055 P. R. China

2. School of Materials Science and Engineering Xiangtan University Xiangtan 411105 P. R. China

3. College of Materials Science and Engineering Qingdao University Qingdao 266000 P. R. China

4. Institute of Flexible Electronics (IFE) Northwestern Polytechnical University (NPU) Xi'an 710072 P. R. China

5. Shenzhen Institutes of Advanced Technology Chinese Academy of Sciences Shenzhen 518055 P. R. China

6. University of Chinese Academy of Sciences Beijing 100049 P. R. China

7. College of New Materials and New Energies Shenzhen Technology University Shenzhen 518118 P. R. China

8. College of Electronics and Information Engineering Shenzhen University Shenzhen 518060 P. R. China

9. Shanghai Synchrotron Radiation Facility Shanghai Advanced Research Institute Chinese Academy of Sciences Shanghai 201204 P. R. China

10. Andlinger Center for Energy and the Environment Princeton University Princeton NJ 08544 USA

11. Department of Chemistry University of Oxford Oxford OX1 3TA UK

12. College of Education Sciences The Hong Kong University of Science and Technology (Guangzhou) Guangzhou 510000 P. R. China

Abstract

AbstractA bromine‐substituted [2‐(9H‐Carbazol‐9‐yl) ethyl] phosphonic acid, 1Br‐2PACz, is designed as hole‐selective self‐assembled monolayers (SAMs), contributing to an outstanding power conversion efficiency (PCE) of 19.35% for binary bulk‐heterojunction (BHJ) based organic solar cells (OSCs). As compared to the previous high‐performance 2Br‐2PACz SAMs, 1Br‐2PACz molecules can effectively reduce the interaction of the SAM with the BTP‐eC9 nonfullerene acceptors with a decreased binding energy, resulting in the suppressed vertical self‐aggregation of BTP‐eC9 small molecules as the bottom side of PM6:BTP‐eC9 BHJ during the solidification process. There is decreased energetic disorder within photoactive layer together with more efficient charge transfer and suppressed non‐radiative recombination. Furthermore, five additional binary BHJ systems are applied in 1Br‐2PACz SAM‐based OSCs, exhibiting continuously superior performance as compared to the reference cells with conventional PEDOT:PSS hole transport layer. This work underscores the potential of advancing OSCs by fine‐tuning SAMs through halogenation strategies to improve active layer morphology and overall device performance.

Funder

National Natural Science Foundation of China

Shenzhen Science and Technology Innovation Program

China Postdoctoral Science Foundation

Basic and Applied Basic Research Foundation of Guangdong Province

Publisher

Wiley

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