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Published on: September 5, 2018
Dynamic Evolution from Chain Disorder to Order of PTB7 Condensed State Structures under External Fields
Jiaxuan Ren1, Xiaona Li1, Tengning Ma1
1State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry , Jilin University , No. 2699 Qianjin Avenue , Changchun 130012 , China.
External fields like solvent, temperature, concentration, and force influence the order of poly[[4,8-bis[(2-ethylhexyl)oxy]benzo[1,2- b:4,5- b]dithiophene-2,6-diyl][3-fluoro-2-[(2-ethylhexyl)carbonyl]thieno[3,4- b]thiophenediyl]] (PTB7) structures. This impacts condensed state structures and optical properties for devices.
Area of Science:
- Materials Science
- Condensed Matter Physics
- Polymer Chemistry
Background:
- The performance of organic electronic devices relies heavily on the condensed state structures of conjugated polymers.
- Controlling the transition from amorphous to ordered states in polymers like PTB7 is crucial for optimizing material properties.
- Understanding the influence of external fields on polymer morphology is essential for material design.
Purpose of the Study:
- To investigate the effect of external fields (solvent, temperature, concentration, force) on the dynamic evolution of PTB7 condensed state structures.
- To correlate structural changes with optical properties using UV-vis absorption spectra and microscopy techniques.
- To provide a physical basis for designing conjugated polymers with enhanced photoelectronic device efficiency.
Main Methods:
- Utilized UV-vis absorption spectroscopy to analyze changes in PTB7 electronic transitions.
- Employed atomic force microscopy (AFM) and transmission electron microscopy (TEM) to visualize morphological changes.
- Varied external conditions including solvent type (1,2-dichloroethane), temperature, solution concentration, and applied force.
Main Results:
- Poor solvent (1,2-dichloroethane) induced amorphous PTB7 conformations.
- Reduced temperature, decreased solution concentration, or increased external force promoted the formation of ordered PTB7 aggregates.
- The ratio of absorption peaks (A0-0/A0-1) increased from 0.94 (amorphous) to 1.25 (large-ordered aggregation), indicating increased order.
Conclusions:
- External fields significantly control the transition from disordered to ordered states in PTB7 condensed structures.
- The observed structural evolution (amorphous, local aggregation, large-scale aggregation) can be monitored via optical and microscopic methods.
- This research offers fundamental insights into polymer self-assembly, vital for tailoring materials for high-performance photoelectronic devices.
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