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Updated: Apr 1, 2026

Monitoring the Effects of Illumination on the Structure of Conjugated Polymer Gels Using Neutron Scattering
Published on: December 21, 2017
Two-dimensional MoS2-assisted immediate aggregation of poly-3-hexylthiophene with high mobility
Yingying Zhang1, Shuang Liu, Wenqing Liu
1MOE Key Laboratory of Macromolecular Synthesis and Functionalization, State Key Laboratory of Silicon Materials, Department of Polymer Science and Engineering, Zhejiang University, Hangzhou 310027, P. R. China. hzchen@zju.edu.cn msxu@zju.edu.cn.
Abstract:
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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