Self‐Organization of Polymer Additive,Poly(2‐vinylpyridine) via One‐Step Solution Processing to Enhance the Efficiency and Stability of Polymer Solar Cells |
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Authors: | Wonho Lee Seonju Jeong Changyeon Lee Gibok Han Changsoon Cho Jung‐Yong Lee Bumjoon J. Kim |
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Affiliation: | 1. Department of Chemical and Biomolecular Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, Republic of Korea;2. Graduate School of Energy Environment Water and Sustainability (EEWS), Korea Advanced Institute of Science and Technology (KAIST), Daejeon, Republic of Korea |
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Abstract: | Interfaces between the photoactive layers and electrodes play critical roles in controlling the performance of optoelectronic devices. Herein, a novel nonconjugated polymer additive (nPA), poly(2‐vinylpyridine) (P2VP), is reported for modifying the interfaces between the bulk‐heterojunction (BHJ) and cathode/metal oxide (MO) layers. The P2VP nPA enables remarkably enhanced power conversion efficiencies (PCEs) and ambient stability in different types of polymer solar cells (PSCs). Importantly, interfacial engineering can be achieved during deposition of the P2VP nPA‐containing BHJ active layer via simple, one‐step solution processing. The P2VP nPA has much higher surface energy than the BHJ active components and stronger interaction with the surface of MO, which affords spontaneous vertical phase separation from the BHJ layer on the MO surface by one‐step solution processing. The self‐assembled P2VP layer substantially reduces the work function and surface defect density of MO, thereby minimizing the charge‐extraction barrier and increasing the PCEs of the PSCs significantly, i.e., PTB7‐Th:PC71BM (10.53%→11.14%), PTB7:PC71BM (7.37%→8.67%), and PTB7‐Th:P(NDI2HD‐T) all‐PSCs (5.52%→6.14%). In addition, the lifetimes of the PSCs are greatly improved by the use of the P2VP nPA. |
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Keywords: | device stability one‐step process polymer additives polymer solar cells work function reduction |
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