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

被引:27
|
作者
Wu, Si-Cheng [1 ]
Strover, Lisa T. [2 ]
Yao, Xiang [1 ]
Chen, Xue-Qiang [1 ]
Xiao, Wen-Jing [1 ]
Liu, Li-Na [1 ]
Wang, Jiandong [1 ]
Visoly-Fisher, Iris [2 ]
Katz, Eugene A. [2 ]
Li, Wei-Shi [1 ,3 ]
机构
[1] Chinese Acad Sci, Ctr Excellence Mol Synth, Shanghai Inst Organ Chem, Key Lab Synthet & Self Assembly Chem Organ Funct, 345 Lingling Rd, Shanghai 200032, Peoples R China
[2] Ben Gurion Univ Negev, Jacob Blaustein Inst Desert Res BIDR, Swiss Inst Dryland Environm & Energy Res, Dept Solar Energy & Environm Phys, Sede Boger Campus, IL-8499000 Midreshet Ben Gurion, Israel
[3] Zhengzhou Inst Technol, Engn Res Ctr Zhengzhou High Performance Organ Fun, Zhengzhou 450044, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
organic photovoltaics; crosslinkable D-A copolymers; thermal stability; photostability; concentrated sunlight; POWER CONVERSION EFFICIENCY; SOLAR-CELLS; MORPHOLOGICAL STABILIZATION; STABILITY; MIXTURES; LINKING; LAYERS;
D O I
10.1021/acsami.8b11506
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
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.
引用
收藏
页码:35430 / 35440
页数:11
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