ACS Appl Mater Interfaces. 2010 Dec;2(12):3422-8. doi: 10.1021/am100922e. Epub 2010 Nov 23.
We demonstrate the utilization of selective functionalization of carbon-silicon (C-Si) alkyl and alkenyl monolayers covalently linked to all-(111) surface silicon nanowire (Si-NW) biosensors. Terminal amine groups on the functional monolayer surfaces were used for conjugation of biotin n-hydroxysuccinimide ester. The selective functionalization is demonstrated by contact angle, X-ray photoelectron spectroscopy (XPS), and high-resolution scanning electron microscopy (HRSEM) of 5 nm diameter thiolated Au nanoparticles linked with streptavidin and conjugated to the biotinylated all-(111) surface Si-NWs. Electrical measurements of monolayer passivated Si-NWs show improved device behavior and performance. Furthermore, an analytical model is presented to demonstrate the improvement in detection sensitivity of the alkyl and alkenyl passivated all-(111) Si-NW biosensors compared to conventional nanowire biosensor geometries and silicon dioxide passivation layers as well as interface design and electrical biasing guidelines for depletion-mode sensors.
我们展示了碳硅 (C-Si) 烷基和烯基单层的选择性功能化在全 (111) 表面硅纳米线 (Si-NW) 生物传感器中的应用。功能单层表面上的末端胺基团用于生物素 n-羟基琥珀酰亚胺酯的缀合。通过接触角、X 射线光电子能谱 (XPS) 和直径为 5nm 的巯基化 Au 纳米粒子与链霉亲和素的连接以及与生物素化全 (111) 表面 Si-NWs 的连接,证明了选择性功能化。单层钝化 Si-NWs 的电测量显示出改善的器件行为和性能。此外,提出了一个分析模型,以证明与传统的纳米线生物传感器几何形状和二氧化硅钝化层以及耗尽模式传感器的界面设计和电偏置指南相比,烷基和烯基钝化的全 (111) Si-NW 生物传感器在检测灵敏度方面的提高。