arXiv subjects
Publications and source records attributed to D. J. Richardson.
We propose an operating principle to achieve broadband and highly tunable mode conversion and amplification exploiting inter-modal four wave mixing in a multimode fiber. A bandwidth of 30 nanometers is demonstrated by properly designing a simple step-index silica fiber.
Optical communications technology has made enormous and steady progress for several decades, providing the key resource in our increasingly information-driven society and economy. Much of this progress has been in finding innovative ways to increase the data carrying capacity of a single optical fibre. In this search, researchers have explored (and close to maximally exploited) every available degree of freedom, and even commercial systems now utilize multiplexing in time, wavelength, polarization, and phase to speed more information through the fibre infrastructure. Conspicuously, one potentially enormous source of improvement has however been left untapped in these systems: fibres can easily support hundreds of spatial modes, but today's commercial systems (single-mode or multi-mode) make no attempt to use these as parallel channels for independent signals.
Simultaneous measurements of the intensity and phase of a probe wave reflected from an interface between silica and elemental alpha-gallium reveal its very strong optical nonlinearity, affecting both these parameters of the reflected wave. The data corroborate with a non-thermal mechanism of optical response which assumes appearance of a homogeneous highly metallic layer, only a few nanometer thick, between the silica and bulk alpha-gallium.
Transient pump-probe optical reflectivity measurements of the nano/microsecond dynamics of a fully reversible, light-induced, surface-assisted metallization of gallium interfaced with silica are reported. The metallization leads to a considerable increase in the interface's reflectivity when solid a-gallium is on the verge of melting. The reflectivity change was found to be a cumulative effect that grows with light intensity and pulse duration. The reflectivity relaxes back to that of alpha-gallium when the excitation is withdrawn in a time that increases critically at gallium's melting point. The effect is attributed to a non-thermal light-induced structural phase transition.