Source abstract
Abstract
The thermomechanical properties of conjugated polymers (CPs) play a crucial role in device morphological, mechanical, and thermal stability and influence device processing parameters. However, the thermal transition behavior of CPs can be difficult to characterize, particularly as the molecular complexity increases. Here, we introduce a characterization technique that is an effective and sensitive approach to observing and defining thermal transitions in CPs. Our approach combines strain alignment with in situ polarized ultraviolet–visible absorption spectroscopy, which we name AFIPS. By monitoring changes in the absorption spectra and dichroism, we demonstrate the ability to effectively identify and characterize thermal transitions undetected using calorimetry. We use this in situ characterization method along with dynamic mechanical analysis (DMA) to probe the thermal transitions of various CPs, including F8T2, P3HT, PCDTBT, PTB7-Th, PM6, and PBnDT-FTAZ. We show that the measurement has a unique response to glass transitions ( T g ), cold crystallization ( T cc ), liquid crystal transitions, and melting. In this investigation, we uncover signatures of a T g in PTB7-Th and a T cc in PCDTBT. Using the AFIPS technique complements other thermomechanical measurements, such as DMA, while being simple and effective to implement, providing a valuable tool for polymer thin film characterization.
Source: openalex_inverted_index · Quality: baseline
Affiliations
Department of Mechanical and Aerospace Engineering and Organic and Carbon Electronics Laboratories (ORaCEL), North Carolina State University, Raleigh, North Carolina 27695, United States
Department of Materials Science and Engineering and ORaCEL, North Carolina State University, Raleigh, North Carolina 27695, United States
Department of Physics, North Carolina State University, Raleigh, North Carolina 27695, United States
Department of Chemistry, University of North Carolina, Chapel Hill, North Carolina 27599, United States
Funding
Office of Naval Research · National Science Foundation