...
首页> 外文期刊>ACS nano >The Shear Flow Processing of Controlled DNA Tethering and Stretching for Organic Molecular Electronics
【24h】

The Shear Flow Processing of Controlled DNA Tethering and Stretching for Organic Molecular Electronics

机译:有机分子电子的受控DNA束缚和拉伸的剪切流处理

获取原文
获取原文并翻译 | 示例
           

摘要

DNA has been recently explored as a powerful tool for developing molecular scaffolds for making reproducible and reliable metal contacts to single organic semiconducting molecules. A critical step in the process of exploiting DNA?organic molecule?DNA (DOD) array structures is the controlled tethering and stretching of DNA molecules. Here we report the development of reproducible surface chemistry for tethering DNA molecules at tunable density and demonstrate shear flow processing as a rationally controlled approach for stretching/aligning DNA molecules of various lengths. Through enzymatic cleavage of λ-phage DNA to yield a series of DNA chains of various lengths from 17.3 μm down to 4.2 μm, we have investigated the flow/extension behavior of these tethered DNA molecules under different flow strengths in the flow-gradient plane. We compared Brownian dynamic simulations for the flow dynamics of tethered λ-DNA in shear, and found our flow-gradient plane experimental results matched well with our bead?spring simulations. The shear flow processing demonstrated in our studies represents a controllable approach for tethering and stretching DNA molecules of various lengths. Together with further metallization of DNA chains within DOD structures, this bottom-up approach can potentially enable efficient and reliable fabrication of large-scale nanoelectronic devices based on single organic molecules, therefore opening opportunities in both fundamental understanding of charge transport at the single molecular level and many exciting applications for ever-shrinking molecular circuits.
机译:最近,DNA被探索为开发分子支架的有力工具,该分子支架使单个有机半导体分子可重现和可靠地与金属接触。利用DNA?有机分子?DNA(DOD)阵列结构的关键步骤是对DNA分子的束缚和伸展。在这里,我们报告了可重现的表面化学的发展,以可调节的密度束缚DNA分子,并证明了剪切流处理是一种合理控制的方法,用于拉伸/对齐各种长度的DNA分子。通过酶切λ噬菌体DNA产生一系列长度从17.3μm到4.2μm的DNA链,我们研究了这些束缚DNA分子在流动梯度平面中不同流动强度下的流动/延伸行为。我们比较了布朗动力学模拟在剪切过程中束缚的λ-DNA的流动动力学,发现我们的流动梯度平面实验结果与我们的弹珠弹簧模拟非常吻合。我们的研究表明,剪切流处理代表了可束缚和拉伸各种长度的DNA分子的可控方法。结合DOD结构中DNA链的进一步金属化,这种自下而上的方法可以潜在地实现基于单个有机分子的高效,可靠的大规模纳米电子器件的制造,从而为在单个分子水平上对电荷传输的基本理解提供了机会以及不断缩小的分子电路的许多令人兴奋的应用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号