Physical Aging Behavior of the Side Chain of a Conjugated Polymer PBTTT

Author:

Qu Tengfei12,Meng Fanzhang1,Li Linling13,Zhang Chen13,Wang Xiaoliang1ORCID,Chen Wei1ORCID,Xue Gi1,Zhuravlev Evgeny14ORCID,Luo Shaochuan15,Zhou Dongshan1

Affiliation:

1. State Key Laboratory of Coordination Chemistry, Department of Polymer Science and Engineering, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210023, China

2. University and College Key Lab of Natural Product Chemistry and Application in Xinjiang, School of Chemistry and Environmental Science, Yili Normal University, Yining 835000, China

3. Institute of Critical Materials for Integrated Circuits, Shenzhen Polytechnic, Shenzhen 518055, China

4. School of Chemistry and Materials Science, Nanjing University of Information Science & Technology, Nanjing 210044, China

5. School of Environment and Energy, Peking University Shenzhen Graduate School, Shenzhen 518055, China

Abstract

This paper provides a viewpoint of the technology of the fast-scanning calorimetry with the relaxation behavior of disordered side chains of poly[2,5-bis(3-dodecylthiophen-2-yl)thieno[3,2-b]thiophene] (PBTTT-C12) around the glass transition temperature of the side chains (Tg,γ). PBTTT is an ideal model of the high-performance copolymer of poly(alkylthiophenes) with side chains. The γ1 relaxation process of the disordered side chains of PBTTT was detected as a small endothermic peak that emerges before the γ2 relaxation process. It shows an increase with increasing temperature as it approaches the glass transition temperature of the disordered side chains of PBTTT. The ductile–brittle transition of PBTTT in low temperatures originating from the thermal relaxation process is probed and illustrated by physical aging experiments. The signature is shown that the relaxation process of the disordered side chain of PBTTT at low temperatures varies from Arrhenius temperature dependence to super Arrhenius temperature dependence at high temperatures. These observations could have significant consequences for the stability of devices based on conjugated polymers, especially those utilized for stretchable or flexible applications, or those demanding mechanical robustness during tensile fabrication or use in a low-temperature environment.

Funder

National Natural Science Foundation of China

Fundamental research funds for the central university

National Key Research and Development Program of China

Guangdong Basic and Applied Basic Research Foundation

Publisher

MDPI AG

Subject

Polymers and Plastics,General Chemistry

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