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

Joonhyeong ChoiDepartment of Chemical and Biomolecular Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141, Republic of KoreaWansun KimDepartment of Mechanical Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141, Republic of KoreaDonguk KimDepartment of Chemical and Biomolecular Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141, Republic of KoreaSeonha KimDepartment of Chemical and Biomolecular Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141, Republic of KoreaJunsu ChaeDepartment of Chemical and Biomolecular Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141, Republic of KoreaSiyoung Q. ChoiDepartment of Chemical and Biomolecular Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141, Republic of KoreaFelix Sunjoo KimSchool of Chemical Engineering and Materials Science, Chung-Ang University (CAU), Seoul 06974, Republic of KoreaTaek‐Soo KimDepartment of Mechanical Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141, Republic of KoreaBumjoon J. KimDepartment of Chemical and Biomolecular Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141, Republic of Korea
2019en
ABI

Аннотация

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 (Mn) ∼ 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 (Mn = 15 kg mol–1). In particular, we observed a jump in the mechanical properties between the Mn = 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.

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