Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States.
J Am Chem Soc. 2011 Jan 19;133(2):203-5. doi: 10.1021/ja108011g. Epub 2010 Dec 17.
The ability to actively manipulate and transport single molecules in solution has the potential to revolutionize chemical synthesis and catalysis. In previous work, we developed a nanopore platform using the interior of a single-walled carbon nanotube (diameter = 1.5 nm) for the Coulter detection of single cations of Li(+), K(+), and Na(+). We demonstrate that as a result of their fabrication, such systems have electrostatic barriers present at their ends that are generally asymmetric, allowing for the trapping of ions. We show that above this threshold bias, traversing the nanopore end is not rate-limiting and that the pore-blocking behavior of two parallel nanotubes follows an idealized Markov process with the electrical potential. Such nanopores may allow for high-throughput linear processing of molecules as new catalysts and separation devices.
主动操纵和输送溶液中单分子的能力有可能彻底改变化学合成和催化。在之前的工作中,我们开发了一种使用单壁碳纳米管(直径= 1.5nm)内部的纳米孔平台,用于库尔特检测锂离子(Li(+)、钾离子(K(+)和钠离子(Na(+)。我们证明,由于它们的制造,这样的系统在其末端存在通常不对称的静电势垒,从而允许捕获离子。我们表明,在这个阈值偏压以上,穿过纳米孔末端不是限速步骤,并且两个平行纳米管的孔阻塞行为遵循理想化的马科夫过程与电势能。这样的纳米孔可能允许作为新的催化剂和分离设备的分子进行高通量线性处理。