RESUMO
We investigate the impact of the photorefractive effect on lithium niobate integrated quantum photonic circuits dedicated to continuous variable on-chip experiments. The circuit main building blocks, i.e. cavities, directional couplers, and periodically poled nonlinear waveguides, are studied. This work demonstrates that photorefractivity, even when its effect is weaker than spatial mode hopping, might compromise the success of on-chip quantum photonics experiments. We describe in detail the characterization methods leading to the identification of this possible issue. We also study to which extent device heating represents a viable solution to counter this effect. We focus on photorefractive effect induced by light at 775 nm, in the context of the generation of non-classical light at 1550 nm telecom wavelength.
RESUMO
Light routing and manipulation are important aspects of integrated optics. They essentially rely on beam splitters which are at the heart of interferometric setups and active routing. The most common implementations of beam splitters suffer either from strong dispersive response (directional couplers) or tight fabrication tolerances (multimode interference couplers). In this paper we fabricate a robust and simple broadband integrated beam splitter based on lithium niobate with a splitting ratio achromatic over more than 130 nm. Our architecture is based on spatial adiabatic passage, a technique originally used to transfer entirely an optical beam from a waveguide to another one that has been shown to be remarkably robust against fabrication imperfections and wavelength dispersion. Our device shows a splitting ratio of 0.52±0.03 and 0.48±0.03 from 1500 nm up to 1630 nm. Furthermore, we show that suitable design enables the splitting in output beams with relative phase 0 or π. Thanks to their independence to material dispersion, these devices represent simple, elementary components to create achromatic and versatile photonic circuits.
RESUMO
Microfluidic separation of magnetic particles is based on their capture by magnetized microcollectors while the suspending fluid flows past the microcollectors inside a microchannel. Separation of nanoparticles is often challenging because of strong Brownian motion. Low capture efficiency of nanoparticles limits their applications in bioanalysis. However, at some conditions, magnetic nanoparticles may undergo field-induced aggregation that amplifies the magnetic attractive force proportionally to the aggregate volume and considerably increases nanoparticle capture efficiency. In this paper, we have demonstrated the role of such aggregation on an efficient capture of magnetic nanoparticles (about 80 nm in diameter) in a microfluidic channel equipped with a nickel micropillar array. This array was magnetized by an external uniform magnetic field, of intensity as low as 6-10 kA/m, and experiments were carried out at flow rates ranging between 0.3 and 30 µL/min. Nanoparticle capture is shown to be mostly governed by the Mason number Ma, while the dipolar coupling parameter α does not exhibit a clear effect in the studied range, 1.4 < α < 4.5. The capture efficiency Λ shows a strongly decreasing Mason number behavior, ΛâMa^{-1.78} within the range 32 ≤ Ma ≤ 3250. We have proposed a simple theoretical model which considers destructible nanoparticle chains and gives the scaling behavior, ΛâMa^{-1.7}, close to the experimental findings.
RESUMO
A temporal shortening by a factor higher than 10 of subnanosecond pulses launched into a low-birefringence optical fiber is achieved by polarization filtering at the output. By means of the theoretical approach, in good agreement with experimental measurements, the impact of the nonlinear polarization rotation and of the coherent coupling phenomena is pointed out.