Isoindigo-Based Binary Polymer Blends for Solution-Processing of Semiconducting Nanofiber Networks AITranslate
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Molecular self-assembly in isoindigo-based binary polymer blends as a novel platform for facile and robust formation of semiconducting nanofibers is studied. We designed structurally complementary polymers to process all-semiconducting nanocomposites. The selection of the tie-polymer for nucleation and nanofiber formation was probed by tuning crystallinity via side chain engineering. Morphology studies revealed that the crystallinity and the scale-like morphology of the tie-polymer play a crucial role in making long and well stacked nanofiber networks. The optimized blends could be solution-processed into nanotailored semiconducting thin films with no postprocessing steps required. The nanofiber formation in thin films further led to lowered elastic moduli and glass transition but higher crack-on-set strain as well as excellent charge transport properties. The formed nanofibers could also be aligned via a blade-directed shearing method to fabricate organic field-effect transistor devices. Our blending strategy shows to be a promising facile route for processing flexible and stretchable organic semiconducting thin films.
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DOI:https://doi.org/10.1021/acsapm.9b00321
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Molecular self-assembly in isoindigo-based binary polymer blends as a novel platform for facile and robust formation of semiconducting nanofibers is studied. We designed structurally complementary polymers to process all-semiconducting nanocomposites. The selection of the tie-polymer for nucleation and nanofiber formation was probed by tuning crystallinity via side chain engineering. Morphology studies revealed that the crystallinity and the scale-like morphology of the tie-polymer play a crucial role in making long and well stacked nanofiber networks. The optimized blends could be solution-processed into nanotailored semiconducting thin films with no postprocessing steps required. The nanofiber formation in thin films further led to lowered elastic moduli and glass transition but higher crack-on-set strain as well as excellent charge transport properties. The formed nanofibers could also be aligned via a blade-directed shearing method to fabricate organic field-effect transistor devices. Our blending strategy shows to be a promising facile route for processing flexible and stretchable organic semiconducting thin films.
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| GB/T 7714-2015 | [1] Aristide Gumyusenge, Xuyi Luo, Hongyi Zhang, et al. ACS Applied Polymer Materials, 2019(1). DOI:10.1021/acsapm.9b00321. |
| MLA | [1] Aristide Gumyusenge, et al., ACS Applied Polymer Materials, no. 1, 2019, https://doi.org/10.1021/acsapm.9b00321. |
| APA | [1] Aristide Gumyusenge, Xuyi Luo, Hongyi Zhang, Gregory M. Pitch, Alexander L. Ayzner, & Jianguo Mei. (2019). ACS Applied Polymer Materials(1). https://doi.org/10.1021/acsapm.9b00321 |
| IEEE | [1] Aristide Gumyusenge, Xuyi Luo, Hongyi Zhang, Gregory M. Pitch, Alexander L. Ayzner, and Jianguo Mei, ACS Applied Polymer Materials, no. 1, 2019, doi: 10.1021/acsapm.9b00321. keywords: {polymer blends;semiconducting nanofibers;organic fieldeffect transistors;stretchable electronics;solution processing} |
