Individual nanoparticles in aqueous solution are observed to be attracted to and orbit within the evanescent sensing ring of a Whispering Gallery Mode micro-sensor with only microwatts of driving power. This Carousel trap, caused by attractive optical gradient forces, interfacial interactions, and the circulating momentum flux, considerably enhances the rate of transport to the sensing region, thereby overcoming limitations posed by diffusion on such small area detectors. Resonance frequency fluctuations, caused by the radial Brownian motion of the nanoparticle, reveal the radial trapping potential and the nanoparticle size. Since the attractive forces draw particles to the highest evanescent intensity at the surface, binding steps are found to be uniform.
We describe and demonstrate a physical mechanism that substantially enhances the label-free sensitivity of a whispering-gallery-mode biosensor for the detection of individual nanoparticles in aqueous solution. It involves the interaction of dielectric nanoparticle in an equatorial carousel orbit with a plasmonic nanoparticle bound at the microparticle's equator. As the dielectric particle parks to hot spots on the plasmonic particle we observe frequency shifts that are enhanced by a factor of 4, consistent with a simple reactive model. Once optimized the enhancement by this mechanism should exceed several orders of magnitude, putting individual protein within reach.
Optofluidic dye lasers hold great promise for adaptive photonic devices, compact and wavelength-tunable light sources, and micro total analysis systems. To date, however, nearly all those lasers are directly excited by tuning the pump laser into the gain medium absorption band. Here we demonstrate bioinspired optofluidic dye lasers excited by FRET, in which the donor-acceptor distance, ratio, and spatial configuration can be precisely controlled by DNA scaffolds. The characteristics of the FRET lasers such as spectrum, threshold, and energy conversion efficiency are reported. Through DNA scaffolds, nearly 100% energy transfer can be maintained regardless of the donor and acceptor concentration. As a result, efficient FRET lasing is achieved at an unusually low acceptor concentration of micromolar, over 1,000 times lower than that in conventional optofluidic dye lasers. The lasing threshold is on the order of μJ∕mm 2 . Various DNA scaffold FRET lasers are demonstrated to illustrate vast possibilities in optofluidic laser designs. Our work opens a door to many researches and applications such as intracavity bio/chemical sensing, biocontrolled photonic devices, and biophysics. O ptofluidic lasers are an emerging technology that combines the advantages of compactness and easy liquid manipulation of microfluidics, and dynamic wavelength tunability and broad spectral coverage of dye lasers (1-3). Optical feedback in those optofluidic lasers has been achieved using high-Q ring resonators [e.g., microdroplets (4, 5), microspheres (6), microcylinders (7), microcapillaries (8, 9), and microfiber knots (10)], Fabry-Pérot cavities (11, 12), and distributed feedback gratings (3, 13). In nearly all those lasers, the gain medium is directly excited by tuning the pump laser into the dye absorption band, which requires that the pump laser wavelength match the particular dye absorption. An alternative excitation scheme is through energy transfer, in which dye mixtures, composed of the donor and the acceptor, are used. Donors are directly excited and subsequently transfer energy to acceptors for lasing. The energy transfer significantly extends the laser emission wavelength range without the need to change the pump wavelength. Moreover, dye lasers based on energy transfer have a much higher pump efficiency and lower lasing threshold than the corresponding single dye lasers due to the low donor absorption loss at the acceptor lasing wavelength (14, 15).Generally, there are two transfer mechanisms between the donor and the acceptor in an optical cavity: nonradiative FRET (14-17), in which the transfer is mediated by short-ranged resonant dipole-dipole interaction, and cavity-assisted radiative transfer (18)(19)(20), in which the emission from the donor is first coupled into the cavity, which stores photons for an extended amount of time before they are reabsorbed by the acceptor. The FRET efficiency between a donor and acceptor pair is R 0 6 ∕ðR 0 6 þ r 6 Þ, where R 0 and r are the Förster distance and the donor-acceptor distance, r...
Optical behavior analogous to electromagnetically induced transparency and absorption is observed in experiments using coupled fused-silica microspheres. This behavior results from interference between coresonant whispering-gallery modes of the two spheres. Coupled-resonator-induced transparency and absorption are observed. Which effect is seen depends on the strength of coupling of incident light from a tapered fiber into the first sphere and on the strength of coupling between the two spheres. The observed effects can enhance microresonator performance in various applications.
The authors demonstrate a microfluidic dye laser using a liquid core optical ring resonator (LCORR). The LCORR is made of a fused silica capillary with a wall thickness of a few microns. The circular cross section of the capillary forms a ring resonator that supports whispering gallery modes (WGMs) and provides an optical feedback for lasers. Due to the high Q factor of the WGM (107), a low lasing threshold is achieved (1μJ∕mm2). In addition, they show that the laser can be coupled out via a tapered fiber in touch with the LCORR, thus providing a mechanism for easy laser delivery.
We developed a novel on-column micro gas chromatography (microGC) detector using capillary based optical ring resonators (CBORRs). The CBORR is a thin-walled fused silica capillary with an inner diameter ranging from a few tens to a few hundreds of micrometers. The interior surface of the CBORR is coated with a layer of stationary phase for gas separation. The circular cross section of the CBORR forms a ring resonator and supports whispering gallery modes (WGMs) that circulate along the ring resonator circumference hundreds of times. The evanescent field extends into the core and is sensitive to the refractive index change induced by the interaction between the gas sample and the stationary phase. The WGM can be excited and monitored at any location along the CBORR by placing a tapered optical fiber against the CBORR, thus enabling on-column real-time detection. Rapid separation of both polar and nonpolar samples was demonstrated with subsecond detection speed. Theoretical work was also established to explain the CBORR detection mechanism. While low-nanogram detection limits are observed in these preliminary tests, many methods for improvements are under investigation. The CBORR is directly compatible with traditional capillary GC columns without any dead volumes. Therefore, the CBORR-based muGC is a very promising technology platform for rapid, sensitive, and portable analytical devices.
Thermo-optic and reactive mechanisms for label-free sensing of bio-particles are compared theoretically for Whispering Gallery Mode (WGM) resonators (sphere, toroid) formed from silica and stimulated into a first order equatorial mode. Although it has been expected that a thermo-optic mechanism should "greatly enhance" wavelength shift signals [A.M. Armani et al, Science 317, 783-787 (2007)] accompanying protein binding on a silica WGM cavity having high Q (10(8)), for a combination of wavelength (680 nm), drive power (1 mW), and cavity size (43 microm radius), our calculations find no such enhancement. The possible reasons for this disparity are discussed.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.