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Nanopore arrays in a silicon membrane for parallel single-molecule detection: fabrication

机译:用于平行单分子检测的硅膜中的纳米孔阵列:制造

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Solid state nanopores enable translocation and detection of single bio-molecules such as DNA in buffer solutions. Here, sub-10 nm nanopore arrays in silicon membranes were fabricated by using electron-beam lithography to define etch pits and by using a subsequent electrochemical etching step. This approach effectively decouples positioning of the pores and the control of their size, where the pore size essentially results from the anodizing current and time in the etching cell. Nanopores with diameters as small as 7 nm, fully penetrating 300 nm thick membranes, were obtained. The presented fabrication scheme to form large arrays of nanopores is attractive for parallel bio-molecule sensing and DNA sequencing using optical techniques. In particular the signal-to-noise ratio is improved compared to other alternatives such as nitride membranes suffering from a high-luminescence background.
机译:固态纳米孔可实现缓冲液中单个生物分子(如DNA)的移位和检测。在此,通过使用电子束光刻来定义蚀刻坑并使用随后的电化学蚀刻步骤,来制造硅膜中的亚10纳米孔阵列。这种方法有效地分离了孔的位置和对孔的大小的控制,其中孔的大小主要是由蚀刻池中的阳极氧化电流和时间导致的。获得了直径小至7 nm,完全穿透300 nm厚膜的纳米孔。提出的形成纳米孔大阵列的制造方案对于使用光学技术的并行生物分子感测和DNA测序具有吸引力。特别是,与其他替代方案(例如遭受高发光背景的氮化物膜)相比,信噪比得到了改善。

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