4.6 Article

Two-dimensional MoS2-assisted immediate aggregation of poly-3-hexylthiophene with high mobility

Journal

PHYSICAL CHEMISTRY CHEMICAL PHYSICS
Volume 17, Issue 41, Pages 27565-27572

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c5cp05011a

Keywords

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Funding

  1. National Natural Science Foundation of China [91233114, 51472219, 51261130582]
  2. Program for New Century Excellent Talents in University [NCET-12-0494]
  3. Research Fund for the Doctoral Program of Higher Education [20130101110123]
  4. Program for 14th China-Japan ST Cooperation [2013DFG52800]
  5. Major State Basic Research Development Program [2014CB643503]
  6. program for Innovative Research Team in University of Ministry of Education of China [IRT13R54]

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Nanoscale morphology is of significance to the electronic properties of semiconducting polymers. Solution-processed poly-3-hexylthiophene (P3HT) has been demonstrated as a promising active-layer material in organic thin film transistors (OTFTs) and solar cells. Controlling the crystallinity of P3HT chains is critical for gaining high-performance devices. Here we demonstrated the immediate crystallization of P3HT induced by two-dimensional MoS2 nanosheets under ultrasonication. The resulting aggregation was attributed to the presence of interaction between the MoS2 nanosheets and P3HT, which could enhance the inter-chain ordering and association of P3HT. The crystallization of P3HT contributed to the 38-fold enhancement in the hole mobility of the thin film as compared to the non-crystallized thin films because of the absence of MoS2. Our approach of using 2D MoS2 nanosheets to induce immediate aggregation of P3HT provides a facile process to control the crystallization of conjugated polymers for the development of high-performance organic electronics.

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