Department of Electrical and Systems Engineering, Washington University in St. Louis, Missouri 63130, USA.
Nat Nanotechnol. 2011 Jun 26;6(7):428-32. doi: 10.1038/nnano.2011.99.
There is a strong demand for portable systems that can detect and characterize individual pathogens and other nanoscale objects without the use of labels, for applications in human health, homeland security, environmental monitoring and diagnostics. However, most nanoscale objects of interest have low polarizabilities due to their small size and low refractive index contrast with the surrounding medium. This leads to weak light-matter interactions, and thus makes the label-free detection of single nanoparticles very difficult. Micro- and nano-photonic devices have emerged as highly sensitive platforms for such applications, because the combination of high quality factor Q and small mode volume V leads to significantly enhanced light-matter interactions. For example, whispering gallery mode microresonators have been used to detect and characterize single influenza virions and polystyrene nanoparticles with a radius of 30 nm (ref. 12) by measuring in the transmission spectrum either the resonance shift or mode splitting induced by the nanoscale objects. Increasing Q leads to a narrower resonance linewidth, which makes it possible to resolve smaller changes in the transmission spectrum, and thus leads to improved performance. Here, we report a whispering gallery mode microlaser-based real-time and label-free detection method that can detect individual 15-nm-radius polystyrene nanoparticles, 10-nm gold nanoparticles and influenza A virions in air, and 30 nm polystyrene nanoparticles in water. Our approach relies on measuring changes in the beat note that is produced when an ultra-narrow emission line from a whispering gallery mode microlaser is split into two modes by a nanoscale object, and these two modes then interfere. The ultimate detection limit is set by the laser linewidth, which can be made much narrower than the resonance linewidth of any passive resonator. This means that microlaser sensors have the potential to detect objects that are too small to be detected by passive resonator sensors.
人们强烈需求能够在无需使用标记的情况下检测和识别个体病原体和其他纳米级物体的便携式系统,这些系统在人类健康、国土安全、环境监测和诊断方面有广泛的应用。然而,大多数感兴趣的纳米级物体由于其尺寸小且与周围介质的折射率对比度低,极化率较低。这导致光物质相互作用较弱,因此使得对单个纳米粒子的无标记检测变得非常困难。微纳光子器件已成为此类应用的高灵敏度平台,因为高品质因数 Q 和小模式体积 V 的结合导致了显著增强的光物质相互作用。例如, whispering gallery 模式微谐振器已被用于通过测量纳米级物体引起的传输光谱中的共振位移或模式分裂来检测和识别单个流感病毒粒子和半径为 30nm 的聚苯乙烯纳米粒子(参考文献 12)。增加 Q 会导致共振线宽变窄,从而可以分辨出传输光谱中较小的变化,从而提高性能。在这里,我们报告了一种基于 whispering gallery 模式微激光的实时和无标记检测方法,该方法可以在空气中检测单个 15nm 半径的聚苯乙烯纳米粒子、10nm 金纳米粒子和流感 A 病毒粒子,以及在水中检测 30nm 的聚苯乙烯纳米粒子。我们的方法依赖于测量当 whispering gallery 模式微激光的超窄发射线被纳米级物体分成两个模式,然后这两个模式干涉时产生的拍频信号的变化。最终的检测极限由激光线宽决定,激光线宽可以比任何无源谐振器的共振线宽窄得多。这意味着微激光传感器有可能检测到太小而无法被无源谐振器传感器检测到的物体。