Majumder Mainak, Zhan Xin, Andrews Rodney, Hinds Bruce J
Department of Chemical & Materials Engineering, University of Kentucky, Lexington, Kentucky 40506-0046, USA.
Langmuir. 2007 Jul 31;23(16):8624-31. doi: 10.1021/la700686k. Epub 2007 Jul 7.
Membranes composed of an array of aligned carbon nanotubes, functionalized with charged molecular tethers, show voltage gated control of ionic transport through the cores of carbon nanotubes. The functional density of tethered charge molecules is substantially increased by the use of electrochemical grafting of diazonium salts. Functionality can be forced to occur at the CNT tip entrances by fast fluid flow of an inert solvent through the core during electrochemical functionalization. The selectivity between Ru(bi-pyridine)(3)2+ and methyl viologen2+ flux is found to be as high as 23 with -130 mV bias applied to the membrane as the working electrode. Changes in the flux and selectivity support a model where charged tethered molecules at the tips are drawn into the CNT core at positive bias. For molecules grafted along the CNT core, negative bias extends the tethered molecules into the core. Electrostatically actuated tethers induce steric hindrance in the CNT core to mimic voltage gated ion channels in a robust large area platform.
由排列整齐的碳纳米管阵列组成的膜,通过带电分子链进行功能化,显示出对通过碳纳米管核心的离子传输的电压门控控制。通过使用重氮盐的电化学接枝,接枝电荷分子的功能密度大幅增加。在电化学功能化过程中,通过惰性溶剂快速流过核心,可迫使功能在碳纳米管尖端入口处发生。当将膜作为工作电极施加-130 mV偏压时,发现Ru(联吡啶)(3)2+和甲基紫精2+通量之间的选择性高达23。通量和选择性的变化支持了这样一个模型:在正偏压下,尖端带电荷的接枝分子被吸入碳纳米管核心。对于沿碳纳米管核心接枝的分子,负偏压会使接枝分子延伸到核心中。静电驱动的链在碳纳米管核心中产生空间位阻,以在坚固的大面积平台中模拟电压门控离子通道。