Optimizing the Crystallization Behavior and Film Morphology of Donor-Acceptor Conjugated Semiconducting Polymers by Side-Chain-Solvent Interaction in Nonpolar Solvents

被引:62
作者
Li, Hongxiang [1 ,2 ]
Yang, Hua [3 ]
Zhang, Lu [1 ,2 ]
Wang, Sichun [1 ,2 ]
Chen, Yu [4 ]
Zhang, Qiang [1 ]
Zhang, Jidong [1 ,2 ]
Tian, Hongkun [1 ,2 ]
Han, Yanchun [1 ,2 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
[2] Univ Sci & Technol China, Sch Appl Chem & Engn, Hefei 230026, Peoples R China
[3] Spallat Neutron Source Sci Ctr, Dongguan 523803, Peoples R China
[4] Chinese Acad Sci, Inst High Energy Phys, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
X-RAY-SCATTERING; CHARGE-TRANSPORT; MOBILITY; CONFORMATION; PHASE; AGGREGATION; ORIENTATION; ALIGNMENT; ORDER; POLY(3-HEXYLTHIOPHENE);
D O I
10.1021/acs.macromol.1c01347
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The solution state of a conjugated polymer plays a critical role in the film morphology and charge carrier mobility of the solution process organic field-effect transistors (OFETs). However, it remains challenging to establish the relationship between solution-state and solid-state morphologies. Herein, we report an effective strategy to control the film formation process and film morphology by regulating the solution state, specifically, through the interaction between the branched side chain of poly[4-(4,4-bis(2-octyldodecyl)-4H-cydopenta[ 1,2-b :5,4-b']dithiophen-2-yl)-alt- [1,2,5]-thiadiazolo [3,4-c] pyridine] (PCDTPT-ODD) and the nonpolar solvent. A precise adjustment of the solution state using the Hansen solubility parameter distance (R-a) has been achieved. Compared to the polar solvent, ordered aggregates were formed in the solution formed by nonpolar solvents. Interestingly, a highly ordered chain arrangement was observed in solutions with suitable R-a's (8.2 and 9.4 MPa1/2 for hexane and isooctane, respectively). Importantly, solution-state aggregation was maintained in the drop-casting film due to the memory effect; the as-prepared films were composed of different fiber sizes and crystal regions. The fiber consisted of a face-on region, with the polymer chains in the fiber aligned perpendicular to the long axis of the fibers. The crystallization process of the edge-on region was independent of the face-on region. The face-on and edge-on regions were produced through the aggregated and disordered parts, respectively. As the R-a increased, the fiber size and the face-on region content increased. Finally, the OFET device mobility was optimized with a significant increase in mu (from 9.7 x 10(-5) to 1.3 x 10(-3) cm(2) V-1 s(-1)). These results showed that the precise regulations of the solution state by the side-chain-solvent interaction play an important role in the film formation process, film morphology, crystallization behavior, and device properties.
引用
收藏
页码:10557 / 10573
页数:17
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