Polarization maintaining single-mode low-loss hollow-core fibres.

Hollow-core fibre (HCF) is a powerful technology platform offering breakthrough performance improvements in sensing, communications, higher-power pulse delivery and other applications. Free from the usual constraints on what materials can guide light, it promises qualitatively new and ideal operating regimes: precision signals transmitted free of nonlinearities, sensors that guide light directly in the samples they are meant to probe and so on. However, these fibres have not been widely adopted, largely because uncontrolled coupling between transverse and polarization modes overshadows their benefits. To deliver on their promises, HCFs must retain their unique properties while achieving the modal and polarization control that are essential for their most compelling applications. Here we present the first single-moded, polarization-maintaining HCF with large core size needed for loss scaling. Single modedness is achieved using a novel scheme for resonantly coupling out unwanted modes, whereas birefringence is engineered by fabricating an asymmetrical glass web surrounding the core.

Low-loss hollow-core fibers with improved single-modedness.

Hollow-core fibers (HCFs) are a revolution in light guidance with enormous potential. They promise lower loss than any other waveguide, but have not yet achieved this potential because of a tradeoff between loss and single-moded operation. This paper demonstrates progress on a strategy to beat this tradeoff: we measure the first hollow-core fiber employing Perturbed Resonance for Improved Single Modedness (PRISM), where unwanted modes are robustly stripped away. The fiber has fundamental-mode loss of 7.5 dB/km, while other modes of the 19-lattice-cell core see loss >3000 dB/km. This level of single-modedness is far better than previous 19-cell or 7-cell HCFs, and even comparable to some commercial solid-core fibers. Modeling indicates this measured loss can be improved. By breaking the connection between core size and single-modedness, this first PRISM demonstration opens a new path towards achieving the low-loss potential of HCFs.

The role of thickness transitions in convective assembly.

Here we examine the microscopic details of convective assembly, a process in which thin colloidal crystals are deposited on a substrate from suspensions of nearly monodisperse spheres. Previously, such crystals have been shown to exhibit a strong tendency toward the face-centered cubic structure, which is difficult to explain on thermodynamic grounds. Using real-time microscopic visualization, electron microscopy, and scanning confocal microscopy, we obtain clues about the crystallization mechanism. Our results indicate that the regions at which a growing crystal transitions from n to n + 1 layers can play an important and previously unrecognized role in the crystallization. For thin crystals, we show both from experiment and through simple modeling that these transition regions can generate specific crystal structures. In thicker crystals, the crystallization is more complicated, but the transition regions must still be considered before a complete understanding of convective assembly can be obtained.

Colloidal crystal layers of hexagonal nanoplates by convective assembly.

Particles of the zeolite ZSM-2 prepared as nearly hexagonal nanoplatelets were coated onto flat substrates by a convective assembly technique. On the submillimeter scale, coatings ranged in patterns from striped to continuous. Particles were preferentially oriented out-of-plane, as supported by X-ray diffractometry. The novel observation is that where the particle coating was only a monolayer thick, particles were locally close-packed and uniformly oriented both in and out of plane in a hexagonal colloidal crystalline arrangement that may be described as being tiled (observations by scanning electron microscopy). This is the first documented demonstration of convective assembly applied to anisometric nanoparticles that resulted in particulate coatings with locally ordered microstructure, i.e., colloidal crystallinity.