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通过二噻吩并[3,2-b:2',3'-d]噻吩/噻吩共聚物对半导体电弧放电碳纳米管进行可伸缩和选择性分散,用于薄膜晶体管。

Scalable and selective dispersion of semiconducting arc-discharged carbon nanotubes by dithiafulvalene/thiophene copolymers for thin film transistors.

机构信息

Department of Materials Science & Engineering, Stanford University, Stanford, California 94305, United States.

出版信息

ACS Nano. 2013 Mar 26;7(3):2659-68. doi: 10.1021/nn4000435. Epub 2013 Feb 22.

DOI:10.1021/nn4000435
PMID:23402644
Abstract

We report a simple and scalable method to enrich large quantities of semiconducting arc-discharged single-walled carbon nanotubes (SWNTs) with diameters of 1.1-1.8 nm using dithiafulvalene/thiophene copolymers. Stable solutions of highly individualized and highly enriched semiconducting SWNTs were obtained after a simple sonication and centrifuge process. Molecular dynamics (MD) simulations of polymer backbone interactions with and without side chains indicated that the presence of long alkyl side chains gave rise to the selectivity toward semiconducting tubes, indicating the importance of the roles of the side chains to both solubilize and confer selectivity to the polymers. We found that, by increasing the ratio of thiophene to dithiafulvalene units in the polymer backbone (from pDTFF-1T to pDTFF-3T), we can slightly improve the selectivity toward semiconducting SWNTs. This is likely due to the more flexible backbone of pDTFF-3T that allows the favorable wrapping of SWNTs with certain chirality as characterized by small-angle X-ray scattering. However, the dispersion yield was reduced from pDTFF-1T to pDTFF-3T. MD simulations showed that the reduction is due to the smaller polymer/SWNT contact area, which reduces the dispersion ability of pDTFF-3T. These experimental and modeling results provide a better understanding for future rational design of polymers for sorting SWNTs. Finally, high on/off ratio solution-processed thin film transistors were fabricated from the sorted SWNTs to confirm the selective dispersion of semiconducting arc-discharge SWNTs.

摘要

我们报告了一种简单且可扩展的方法,使用二噻吩并[3,2-b:2',3'-d]呋喃/噻吩共聚物从直径为 1.1-1.8nm 的电弧放电单壁碳纳米管(SWNTs)中高效富集大量半导体 SWNTs。经过简单的超声和离心处理后,得到了高度单分散和高度富集的半导体 SWNTs 的稳定溶液。聚合物主链与无侧链相互作用的分子动力学(MD)模拟表明,长烷基侧链的存在导致对半导体管的选择性,表明侧链对聚合物的溶解和选择性赋予的重要作用。我们发现,通过增加聚合物主链中噻吩与二噻吩并[3,2-b:2',3'-d]呋喃单元的比例(从 pDTFF-1T 到 pDTFF-3T),我们可以略微提高对半导体 SWNTs 的选择性。这可能是由于 pDTFF-3T 的柔性主链允许某些手性的 SWNTs 进行有利的包裹,这在手性小角 X 射线散射中得到了证实。然而,分散产率从 pDTFF-1T 降低到了 pDTFF-3T。MD 模拟表明,减少的原因是聚合物/SWNT 的接触面积较小,这降低了 pDTFF-3T 的分散能力。这些实验和模拟结果为未来合理设计用于分离 SWNTs 的聚合物提供了更好的理解。最后,从分离出的 SWNTs 制备了具有高开关比的溶液处理薄膜晶体管,以确认半导体电弧放电 SWNTs 的选择性分散。

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