Nano-fabrication dependent quality factor in photonic crystal slab biosensors

H. Akhavan, M. El-Beheiry, O. Levi
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引用次数: 5

Abstract

Photonic crystal slabs (PCS) are attractive for label-fr ee optical bio-sensors inside micro-fluidic portable diagnostic systems due to their high sensitivity and easy coupling to external radiation. Obtaining high quality factor (Q) values for the guided resonances in these index-of-refraction PCS biosensors is crucial for high sensitivity. Non-ideal fabrication of the hole array in the PCS due to electron beam writing, pattern transfer, and reactive ion etching (RIE) steps will result in imperfect circular hole shapes, and non vertical hole profile that can reduce the Q values. We evaluate the effect of nano-fabrication on the quality factor of guided resonances in PCS biosensors and investigate the potential limitations on sensitivity with current fabrication technologies in a realistic PCS biosensor due to fabrication errors. Spectral broadening of the guided resonances (lower Q values) is found for the fundamental guided resonance modes but no significant changes were observed in higher order guided resonances. These fin dings are consistent with reduced bio-sensing sensitivity in higher order modes due to reduced field overlap with the analyte in side the micro-fluidic channels.
光子晶体板型生物传感器中纳米制造依赖的质量因子
光子晶体板具有高灵敏度、易与外界辐射耦合的特点,是微流控便携式诊断系统中无标签光学生物传感器的重要组成部分。获得高质量因子(Q)值的引导共振在这些折射率的PCS生物传感器是高灵敏度的关键。由于电子束写入、图案转移和反应离子刻蚀(RIE)步骤,导致PCS中空穴阵列的不理想制造将导致圆孔形状不完美,并且非垂直的空穴轮廓会降低Q值。我们评估了纳米制造对PCS生物传感器中引导共振质量因子的影响,并研究了当前制造技术在实际PCS生物传感器中由于制造误差而对灵敏度的潜在限制。基阶导共振模式的谱增宽(Q值较低),而高阶导共振模式的谱无明显变化。这些发现与高阶模式下生物传感灵敏度的降低是一致的,这是由于微流体通道侧与分析物的场重叠减少。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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