Direct observation of self-similarity in evolution of transient stimulated Raman scattering in gas-filled photonic crystal fibers.

A unique characteristic of transient stimulated Raman scattering, in which the spatiotemporal evolution of the fields and the molecular excitation follow a universal self-similarity law, is observed in gas-filled photonic crystal fibers. As the input laser power is increased, the coupled system "optical fields + molecular excitation" goes through the same phases of time evolution but at a higher rate. Using the self-similarity law we are able to completely reconstruct the evolution of the pump and Stokes fields from one measurement.

Solitary pulse generation by backward Raman scattering in H2-filled photonic crystal fibers.

Using a hydrogen-filled hollow-core photonic crystal fiber as a nonlinear optical gas cell, we study amplification of ns-laser pulses by backward rotational Raman scattering. We find that the amplification process has two characteristic stages. Initially, the pulse energy grows and its duration shortens due to gain saturation at the trailing edge of the pulse. This phase is followed by formation of a symmetric pulse with a duration significantly shorter than the phase relaxation time of the Raman transition. Stabilization of the Stokes pulse profile to a solitonlike hyperbolic secant shape occurs as a result of nonlinear amplification at its front edge and nonlinear absorption at its trailing edge (caused by energy conversion back to the pump field), leading to a reshaped pulse envelope that travels at superluminal velocity.