This work presents an optical humidity sensing technique based on the combination of a whispering gallery mode microtoroidal cavity sensor and a nm-scale thick humidity-responsive polymer coating deposited via the initiated chemical vapor deposition process. As a result of the conformational change by the polymer in response to humidity, the sensitivity is increased by nearly two orders of magnitude in comparison to conventional refractometric sensing. Additionally, the dependence of the device performance on the film thickness is studied. Specifically, the thinner film enabled a faster response rate, yet a slower recovery rate, as compared to the thicker films.

Label-free sensors based on electrical, mechanical and optical transduction methods have potential applications in numerous areas of society, ranging from healthcare to environmental monitoring. Initial research in the field focused on the development and optimization of various sensor platforms fabricated from a single material system, such as fiber-based optical sensors and silicon nanowire-based electrical sensors. However, more recent research efforts have explored designing sensors fabricated from multiple materials. For example, synthetic materials and/or biomaterials can also be added to the sensor to improve its response toward analytes of interest. By leveraging the properties of the different material systems, these hybrid sensing devices can have significantly improved performance over their single-material counterparts (better sensitivity, specificity, signal to noise, and/or detection limits). This review will briefly discuss some of the methods for creating these multi-material sensor platforms and the advances enabled by this design approach.

Optical resonant microcavities with ultra high quality factors are widely used for biosensing. Until now, the primary method of detection has been based upon tracking the resonant wavelength shift as a function of biodetection events. One of the sources of noise in all resonant-wavelength shift measurements is the noise due to intensity fluctuations of the laser source. An alternative approach is to track the change in the quality factor of the optical cavity by using phase shift cavity ring down spectroscopy, a technique which is insensitive to the intensity fluctuations of the laser source. Here, using biotinylated microtoroid resonant cavities, we show simultaneous measurement of the quality factor and the wavelength shift by using phase shift cavity ring down spectroscopy. These measurements were performed for disassociation phase of biotin-streptavidin reaction. We found that the disassociation curves are in good agreement with the previously published results. Hence, we demonstrate not only the application of phase shift cavity ring down spectroscopy to microcavities in the liquid phase but also simultaneous measurement of the quality factor and the wavelength shift for the microcavity biosensors in the application of kinetics measurements.

Whispering gallery mode optical resonant cavities fabricated from rare-earth-doped silica glasses have demonstrated lasing from the visible through the near-IR. However, achieving lasing in the blue has been elusive. In this Letter, thulium-doped silica films are synthesized and used to fabricate toroidal optical microcavities with quality factors in excess of 10 million. Despite the high phonon energy of silica, the high circulating optical intensities present in the microcavities enable upconversion of the thulium, resulting in emission in the blue and near-IR with microwatt threshold powers that scale linearly with the concentration of the thulium.

Optical microcavities are high sensitivity transducers able to detect single nanoparticles and molecules. However, the specificity of detection is dependent on the availability of an appropriate targeting moiety with minimal cross-reactivity. In the present work, an alternative approach is shown. Namely, using biotin-functionalized toroidal microcavities, the dissociation constant of biotin to two different streptavidin complexes (free and polystyrene bead) is determined. Based on the difference in affinity and in mass transport, the two complexes are identified from a mixture. By leveraging information in the binding site, improved specificity can be achieved.