Monitoring the Effects of Illumination on the Structure of Conjugated Polymer Gels Using Neutron Scattering

被引:1
作者
Morgan, Brian [1 ]
Rinehart, Samantha J. [1 ]
Dadmun, Mark D. [1 ,2 ]
机构
[1] Univ Tennessee, Dept Chem, Knoxville, TN 37996 USA
[2] Oak Ridge Natl Lab, Chem Sci Div, Oak Ridge, TN 37830 USA
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2017年 / 130期
基金
美国国家科学基金会;
关键词
Chemistry; Issue; 130; Optically active polymers; conjugated polymers; polymer gels; small angle neutron scattering; stimuli-responsive materials; thermo-reversible; CHARGE-TRANSPORT; MEH-PPV; POLY(3-HEXYLTHIOPHENE); MORPHOLOGY; FULLERENE; PERFORMANCE; GELATION; SOLVENT; TRANSITION; EMISSION;
D O I
10.3791/56163
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We demonstrate a protocol to effectively monitor the gelation process of a high concentration solution of conjugated polymer both in the presence and absence of white light exposure. By instituting a controlled temperature ramp, the gelation of these materials can be precisely monitored as they proceed through this structural evolution, which effectively mirrors the conditions experienced during the solution deposition phase of organic electronic device fabrication. Using small angle neutron scattering (SANS) and ultra-small angle neutron scattering (USANS) along with appropriate fitting protocols we quantify the evolution of select structural parameters throughout this process. Thorough analysis indicates that continued light exposure throughout the gelation process significantly alters the structure of the ultimately formed gel. Specifically, the aggregation process of poly(3-hexylthiophene-2,5-diyl) (P3HT) nano-scale aggregates is negatively affected by the presence of illumination, ultimately resulting in the retardation of growth in conjugated polymer microstructures and the formation of smaller scale macro-aggregate clusters.
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页数:8
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