Coherent soft x rays are produced by high-harmonic generation in a capillary filled with Ar gas. We demonstrate that the tuning of the harmonic wavelengths with intensity and chirp arises from changes in the Ar ionization level. Control over the tuning can be achieved either by changing the average intensity of the laser pulse or by varying the quadratic spectral phase of the laser pulse. We observe an ionization-dependent blueshift of the fundamental wavelength that is directly imprinted on the harmonic wavelengths. The harmonic tuning is shown to depend on nonlinear spectral shifts of the fundamental laser pulse that are due to the plasma created by ionization, rather than directly on any chirp imposed on the fundamental wavelength.

The use of Raman microspectroscopy to depth profile multi-layered polymer laminates is becoming increasingly popular. However, the results are generally degraded by aberrations introduced by the change in refractive index at the air/sample interface. Recent research has suggested that the use of an immersion oil and suitable objective can reduce this effect. This study evaluates this proposal by comparing depth profiling results on a multi-layer poly(styrene)/poly(methylmethacrylate) (PS/PMMA) laminate polymer from both dry metallurgical objectives and immersion objectives (used in combination with an oil of suitable refractive index). The immersion technique enabled successful depth profiling to the full working distance of the objective (100 microm), showing clear and distinct variations in 11 different layers within the laminate; a dry metallurgical objective used for comparison achieved poor resolution of only two layers. This is the first demonstration of depth profiling within a polymer laminate to this depth. The depth profiling results are compared to results obtained by sectioning the PS/PMMA sample after setting it in resin.

The production of coherent soft x-rays via high harmonic generation (HHG) from Ar, N 2 and N 2 O in a gas-filled capillary waveguide is reported. Odd harmonics of the driving laser intensity are observed as a function of gas pressure up to energies of 50 eV. By employing a simple phase matching theory that incorporates the spatial and temporal dependences of ionization within the waveguide, good agreement with the HHG spectral envelope has been obtained, indicating phase matching is the dominant factor in shaping the spectral envelope of the harmonics.