Browsing by Author "Kalantarifard, Fatemeh"
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Item Open Access Intracavity optical trapping of microscopic particles in a ring-cavity fiber laser(Nature Publishing Group, 2019-06) Kalantarifard, Fatemeh; Elahi, Parviz; Makey, Ghaith; İlday, F. Ömer; Volpe, Giovanni; Maragò, O. M.Standard optical tweezers rely on optical forces arising when a focused laser beam interacts with a microscopic particle: scattering forces, pushing the particle along the beam direction, and gradient forces, attracting it towards the high-intensity focal spot. Importantly, the incoming laser beam is not affected by the particle position because the particle is outside the laser cavity. Here, we demonstrate that intracavity nonlinear feedback forces emerge when the particle is placed inside the optical cavity, resulting in orders-of-magnitude higher confinement along the three axes per unit laser intensity on the sample. This scheme allows trapping at very low numerical apertures and reduces the laser intensity to which the particle is exposed by two orders of magnitude compared to a standard 3D optical tweezers. These results are highly relevant for many applications requiring manipulation of samples that are subject to photodamage, such as in biophysics and nanosciences.Item Open Access Intracavity optical trapping with fiber laser(2019-06) Kalantarifard, FatemehAfter Ashkin's seminal works, optical trapping has been a powerful technique for capturing and manipulating sub micro particles not only in physics research fields but also in biology and photonics. Standard optical tweezers consists of a single beam with Gaussian or profile which focused by a high numerical aperture (NA) water or oil immersion microscope objective. Typically, objective with NA>1.2 is used to provide strong enough gradient forces being able to overcome Brownian uctuations and gravity and trap the particle stably. On the other hand, compare with high NA, trapping with low NA, has its own advantage and among all the advantages, low local heating of the sample has a particular interest in molecular biology and manipulating living cells. The main concern is that the interaction of trapping laser beam and biological object induces a damage on the specimen which is mainly due to light absorption of the sample. It is, therefore, recommended to use NIR (near infrared ) wavelength due to its minimal absorption by water and biological objects. Other important factors that must be considered, to secure the viability of the cell, are spot size of the focused beam and laser power at the sample plane. Thus, it deserves an effort to look for new configurations with low NA with the capability of creating 3D confinement. Standard optical tweezers rely on optical forces that arise when a focused laser beam interacts with a microscopic particle: scattering forces, which push the particle along the beam direction, and gradient forces, which attract it towards the high-intensity focal spot. Importantly, the incoming laser beam is not affected by the particle position because the particle is outside the laser cavity. Here, we demonstrate that intracavity nonlinear feedback forces emerge when the particle is placed inside the optical cavity, resulting in orders-of-magnitude higher confinement per unit laser intensity on the sample. We first present a toy model that intuitively explains how the microparticle position and the laser power become nonlinearly coupled: The loss of the laser cavity depends on the particle position due to scattering, so the laser intensity grows whenever the particle tries to escape. We describe a simple toy model to clarify how the nonlinear feedback forces emerge as a result of the interplay between the particle's motion and the laser's dynamics. It also quantifies how and to what extent this scheme reduces the average laser power to which a trapped particle is exposed. In this model, the power and hence trapping force are considered to be zero for small particle displacements. However, in reality they have small values that do operate the trap even when the particle is near the equilibrium position. Thus, we need an accurate description of the coupling between the laser and the trapped particle thermal dynamics at equilibrium to compare with experiments. In particular, accurate simulations can help to associate an effective harmonic potential to the optical trap for small displacements from the equilibrium position, and hence to define a meaningful stiffness using the standard calibration methods based on the thermal uctuations of a trapped particle. We therefore present a series of numerical simulations based on an extended theoretical model, including highly realistic descriptions of the laser dynamics, optical losses incurred by the particle, and the particle's Brownian motion in order to gain a quantitative understanding of the dynamics of intracavity optical trapping and to guide the experiments. Finally, guided by the simulation results, we have built an experimental setup to prove the operational principle of intracavity optical trapping and experimentally realize this concept by optically trapping microscopic polystyrene and silica particles inside the ring cavity of a fiber laser. One of the major advantages of the intracavity optical trapping scheme is that it can operate with very low-NA lenses, with a consequent large field-of-view, and at very low average power, resulting in about two orders of magnitude reduction in exposure to laser intensity compared to standard optical tweezers. When compared to other low-NA optical trapping schemes, positive and negative aspects can be considered, such as in terms of trap stiffness and average irradiance of the sample. These features can yield advantages when dealing with biological samples. Ultra-low intensity at our wavelength can grant a safe, temperature controlled environment, away from surfaces for micro uidics manipulation of biosamples. Accurate studies on Saccharomices cerevisiae yeast cells in near-infrared counterpropagating traps and standard optical tweezers have found no evidence for a lower power threshold for phototoxicity. We observed that we can 3D trap single yeast cells with about 0:47 mW, corresponding to an intensity of 0:036 mW m2, that is more than a tenfold less intensity than standard techniques.Item Open Access Intracavity optical trapping with ytterbium doped fiber(SPIE, 2013) Laser, R.; Sayed, R.; Kalantarifard, Fatemeh; Elahi P.; İlday, F. Ömer; Volpe, Giovanni; Marago O.M.We propose a novel approach for trapping micron-sized particles and living cells based on optical feedback. This approach can be implemented at low numerical aperture (NA=0.5, 20X) and long working distance. In this configuration, an optical tweezers is constructed inside a ring cavity fiber laser and the optical feedback in the ring cavity is controlled by the light scattered from a trapped particle. In particular, once the particle is trapped, the laser operation, optical feedback and intracavity power are affected by the particle motion. We demonstrate that using this configuration is possible to stably hold micron-sized particles and single living cells in the focal spot of the laser beam. The calibration of the optical forces is achieved by tracking the Brownian motion of a trapped particle or cell and analysing its position distribution. © 2013 SPIE.Item Open Access Real-time image-based droplet measurement(Chemical and Biological Microsystems Society, 2020) Elahi, Sepehr; Kalantarifard, Ali; Kalantarifard, Fatemeh; Elbüken, ÇağlarThe ability to measure physical properties of droplets in real-time is required to design precise operations on droplet-based systems. In this study, we implemented a real-time droplet tracker that tracks the positions of droplets and measures droplet generation frequency as well as droplets' physical properties, such as size, size distribution, shape, velocity, circularity. Furthermore, using the droplet length, we use curve fitting to determine the dispersed phase viscosity. Our droplet tracker is implemented in Python, using the OpenCV library and can be run on a routine PC.