4.8 Article

UV-Cross-linkable Donor-Acceptor Polymers Bearing a Photostable Conjugated Backbone for Efficient and Stable Organic Photovoltaics

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 10, Issue 41, Pages 35430-35440

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.8b11506

Keywords

organic photovoltaics; crosslinkable D-A copolymers; thermal stability; photostability; concentrated sunlight

Funding

  1. National Natural Science Foundation of China [21474129, 21674125, 51761145043]
  2. International Science and Technology Cooperation Program of China [2015DFG62680]
  3. Strategic Priority Research Program of Chinese Academy of Sciences [XDB20020000]
  4. Science and Technology Open Cooperation Projects of Henan Province [162106000018, 172106000067]
  5. Zhengzhou Institute of Technology
  6. Blaustein Center for Scientific Cooperation's postdoctoral fellowship
  7. Israel's Ministry of Science and Technology China-Israel Cooperative Scientific Research fund [3-12387]
  8. Adelis Foundation

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High-performance photovoltaic polymers bearing cross-linkable function together with a photorobust conjugated backbone are highly desirable for organic solar cells to achieve both high device efficiency and long-term stability. In this study, a family of such polymers is reported based on poly[(2,5-bis(2-hexyldecyloxy)phenylene)-alt-(5,6-difluoro-4,7-di(thiophen-2-yObenzo [c]-[1,2,5 thiadiazole) (PPDT2FBT), a high-performance photovoltaic donor acceptor polymer, with different contents of terminal vinyl appended side chains for cross-linking. The polymers were named PPDT2FBT-V and prepared by varying the feeding ratio (x mol %, x = 0, 5, 10, and 15) of the vinyl-appended monomer in polymerization. It was found that the vinyl integration did not sacrifice the original high photovoltaic performance of the polymers, as evidenced by comparable average power conversion efficiencies (PCEs) (6.95, 7.02, and 7.63%) observed for optimized devices based on PPDT2FBT-V-0, PPDT2EBT-V-s, and PPDT2FBT-V-10, respectively, in blending with [6,6]-phenyl-C-71-butyric acid methyl ester (PC71BM). Unlike thermal cross-linking that greatly reduced device efficiency, UV cross-linking has proven to be an effective way to achieve both high device efficiency and thermostability for PPDT2FBT-V-10 solar cells. UV-cross-linked PPDT2FBT-V-10 solar cells displayed an initial average PCE of 5.28% and almost no decrease upon heat treatment at 120 degrees C for 40 h. Morphology studies revealed that UV-cross-linking did not only alter initial nanophase separation but also suppressed morphology evolution by aggregation in bulk heterojunction blend films. Photo-cross-linking requires material photostability. It is therefore worthwhile to note that these polymers and their blends with PC71BM were found to be extremely photostable, even upon continuous exposure to concentrated sunlight (up to 200 suns), and UV-cross-linking does not hamper this photostability. Further studies found that the devices fabricated with the UV-cross-linked PPDT2EBT-V-10/PC71BM active layer can endure continuous light exposure to a solar simulator without deteriorating their performance.

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