Affiliation:
1. Beijing Key Laboratory of Energy Conversion and Storage Materials College of Chemistry Beijing Normal University Beijing 100875 China
2. College of Chemistry and Materials Science Hebei University Baoding 071002 China
3. Shenzhen Key Laboratory of New Information Display and Storage Materials, College of Materials Science and Engineering Shenzhen University Shenzhen 518060 China
4. College of Textiles & Clothing State Key Laboratory of Bio‐fibers and Eco‐textiles Qingdao University Qingdao 266071 China
Abstract
AbstractThe layer‐by‐layer (LbL) solution‐processed organic solar cells (OSCs) are conductive to achieve vertical phase separation, tunable donor–acceptor (D/A) interfaces, and favorable charge‐transport pathways. In this work, a wide‐bandgap component poly(9‐vinylcarbazole) (PVK) is added to the upper electron acceptor layer to improve the performance of LbL‐processed OSCs. Results show that the PVK component can adjust the film morphology, dope the electron acceptor, increase the electron concentration, and improve charge transport. Such n‐type doping is verified by Seebeck coefficient measurement, ultraviolet photoelectron spectroscopy, and electron paramagnetic resonance characterization. In addition, the fluorescence intensity and exciton lifetime of the PVK‐doped acceptor film are increased, thus being beneficial for exciton diffusion to the D/A interface. Therefore, the power conversion efficiency (PCE) of LbL OSCs increases when 2.50 wt.% PVK is employed in the electron acceptor layer of commonly‐used high‐efficiency system and a maximum value of 19.05% can be achieved. The role of PVK played in the active layer is different from those of additives and ternary components reported previously, so the results provide an alternative way to enhance the device performance of LbL‐processed OSCs.
Funder
National Natural Science Foundation of China
Beijing University of Chemical Technology
Subject
Mechanical Engineering,Mechanics of Materials,General Materials Science
Cited by
48 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献