Importance of Critical Molecular Weight of Semicrystalline n-Type Polymers for Mechanically Robust, Efficient Electroactive Thin Films

被引:131
作者
Choi, Joonhyeong [1 ]
Kim, Wansun [2 ]
Kim, Donguk [1 ]
Kim, Seonha [1 ]
Chae, Junsu [1 ]
Choi, Siyoung Q. [1 ]
Kim, Felix Sunjoo [3 ]
Kim, Taek-Soo [2 ]
Kim, Bumjoon J. [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Chem & Biomol Engn, Daejeon 34141, South Korea
[2] Korea Adv Inst Sci & Technol, Dept Mech Engn, Daejeon 34141, South Korea
[3] CAU, Sch Chem Engn & Mat Sci, Seoul 06974, South Korea
基金
新加坡国家研究基金会;
关键词
POWER CONVERSION EFFICIENCY; ALL-POLYMER; SOLAR-CELLS; HIGH-PERFORMANCE; ORGANIC SEMICONDUCTORS; CONJUGATED POLYMERS; FULLERENE-POLYMER; TENSILE-STRENGTH; CHARGE-TRANSPORT; AGGREGATION;
D O I
10.1021/acs.chemmater.8b05114
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Mechanical properties of conducting polymers are an essential consideration in the design of flexible and stretchable electronics, but the guidelines for the material design having both high mechanical and electrical properties remain limited. Here we provide an important guideline for the design of mechanically robust, electroactive polymer thin films in terms of the molecular weight of the polymers. These studies based on a highly efficient, representative n-type conjugated polymer (P(NDI2OD-T2)) revealed a marked enhancement in mechanical properties across a narrow molecular weight range, highlighting the existence of a critical molecular weight that can be exploited to engineer films that balance processability and mechanical and electronic properties. We found the thin films formed from high molecular weight polymers (i.e., number-average molecular weight (M-n) similar to 163 kg mol(-1)) to exhibit superior mechanical compliance and robustness, with a 114-fold enhanced strain at fracture and a 2820-fold enhanced toughness, as compared to those of low molecular weight polymer films (M-n = 15 kg mol(-1)). In particular, we observed a jump in the mechanical properties between the M-n = 48 and 103 kg mol(-1), yielding a 26-fold enhanced strain at fracture and a 160-fold enhanced toughness. The significant improvement of tensile properties indicates the presence of a critical molecular weight at which entangled polymer networks start to form, as supported by the analysis of the thermal and crystalline properties, specific viscosity, and microstructure. Our work provides useful guidelines for the design of conjugated polymers with recommendations for the best combinations of mechanical robustness and electrical performance for flexible and stretchable electronics.
引用
收藏
页码:3163 / 3173
页数:11
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