Micron School of Materials Science & Engineering, Boise State University, Boise, ID 83725, USA.
Department of Electrical & Computer Engineering, Boise State University, Boise, ID 83725, USA.
Int J Mol Sci. 2018 Aug 24;19(9):2513. doi: 10.3390/ijms19092513.
DNA nanostructures routinely self-assemble with sub-10 nm feature sizes. This capability has created industry interest in using DNA as a lithographic mask, yet with few exceptions, solution-based deposition of DNA nanostructures has remained primarily academic to date. En route to controlled adsorption of DNA patterns onto manufactured substrates, deposition and placement of DNA origami has been demonstrated on chemically functionalized silicon substrates. While compelling, chemical functionalization adds fabrication complexity that limits mask efficiency and hence industry adoption. As an alternative, we developed an ion implantation process that tailors the surface potential of silicon substrates to facilitate adsorption of DNA nanostructures without the need for chemical functionalization. Industry standard 300 mm silicon wafers were processed, and we showed controlled adsorption of DNA origami onto boron-implanted silicon patterns; selective to a surrounding silicon oxide matrix. The hydrophilic substrate achieves very high surface selectivity by exploiting pH-dependent protonation of silanol-groups on silicon dioxide (SiO₂), across a range of solution pH values and magnesium chloride (MgCl₂) buffer concentrations.
DNA 纳米结构通常可以自我组装成亚 10nm 的特征尺寸。这种能力引发了业界对 DNA 作为光刻掩模的兴趣,但迄今为止,除了少数例外,基于溶液的 DNA 纳米结构沉积主要仍停留在学术领域。在将 DNA 图案可控地吸附到制造的基底上的过程中,已经在化学功能化的硅基底上演示了 DNA 折纸的沉积和放置。虽然很有吸引力,但化学功能化增加了制造复杂性,限制了掩模效率,从而限制了行业采用。作为替代方法,我们开发了一种离子注入工艺,该工艺可以调整硅基底的表面电势,从而无需化学功能化即可促进 DNA 纳米结构的吸附。对工业标准的 300mm 硅片进行了处理,并展示了将 DNA 折纸可控地吸附到硼注入硅图案上;与周围的氧化硅基质具有选择性。亲水基底通过利用二氧化硅(SiO₂)上硅醇基团的 pH 依赖性质子化作用,在一系列溶液 pH 值和氯化镁(MgCl₂)缓冲浓度下,实现了非常高的表面选择性。