Journal
JOURNAL OF PHYSICAL CHEMISTRY C
Volume 118, Issue 51, Pages 29473-29481Publisher
AMER CHEMICAL SOC
DOI: 10.1021/jp5075797
Keywords
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Funding
- National Natural Science Foundation of China [20974029, 91027031]
- Ministry of Science and Technology of China [2009CB930400, 2010DFB63530, 2011CB932300]
- Chinese Academy of Sciences
- Office of Novel Research [NOOO14-11-1-0211]
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Tailoring the blend morphology in a bulk heterojunction device is of critical importance but remains a challenge today. Although the morphologies of polymer solar cells can be tuned by thermal/solvent annealing or by incorporation of solvent additives, optimizing the morphology of the active layer for a newly synthesized polymer has, to date, remained mostly an empirical approach. In this work, three typical polymers in organic photovoltaics have been studied. By processing at different conditions, each polymer reveals high selectivity in the optimizing methods. Optical spectrum and electrostatic force microscopy results demonstrate morphology as the main reason for various device performances. Further, these can be traced back to the self-assembly behaviors of polymers. By the established relationships between molecular structure, morphology, and the corresponding device performances, we propose a self-assembly based process-selection guideline for efficient performance improvement of newly synthesized materials.
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