Department of Electrical and Computer Engineering, University of Illinois at Urbana-Champaign, Urbana, IL, USA.
Nick Holonyak Jr. Micro and Nanotechnology Laboratory, University of Illinois at Urbana-Champaign, Urbana, IL, USA.
Nat Commun. 2021 Mar 19;12(1):1744. doi: 10.1038/s41467-021-21999-3.
Interferometric scattering microscopy is increasingly employed in biomedical research owing to its extraordinary capability of detecting nano-objects individually through their intrinsic elastic scattering. To significantly improve the signal-to-noise ratio without increasing illumination intensity, we developed photonic resonator interferometric scattering microscopy (PRISM) in which a dielectric photonic crystal (PC) resonator is utilized as the sample substrate. The scattered light is amplified by the PC through resonant near-field enhancement, which then interferes with the <1% transmitted light to create a large intensity contrast. Importantly, the scattered photons assume the wavevectors delineated by PC's photonic band structure, resulting in the ability to utilize a non-immersion objective without significant loss at illumination density as low as 25 W cm. An analytical model of the scattering process is discussed, followed by demonstration of virus and protein detection. The results showcase the promise of nanophotonic surfaces in the development of resonance-enhanced interferometric microscopies.
干涉散射显微镜由于其通过固有弹性散射来单独检测纳米物体的非凡能力,在生物医学研究中得到了越来越多的应用。为了在不增加照明强度的情况下显著提高信噪比,我们开发了光子共振干涉散射显微镜(PRISM),其中介电光子晶体(PC)共振器用作样品衬底。通过共振近场增强,散射光被 PC 放大,然后与<1%的透射光干涉,产生大的强度对比。重要的是,散射光子采用 PC 的光子带结构划定的波矢,从而能够在照明密度低至 25 W/cm2 时使用非浸液物镜而不会有明显损失。讨论了散射过程的分析模型,然后展示了病毒和蛋白质的检测。结果展示了纳米光子表面在发展共振增强干涉显微镜方面的潜力。