LAUSR

Abstract Tightly focused, highly spatially multiplexed femtosecond laser pulses, coming at sub-MHz repetition rates, were used to mask-less pattern thin plasmonic films film at ultrafast rates, approaching 25 million of microelements per second. For this purpose, the initial pulses were multiplexed by fused silica diffractive optical elements into linear arrays of 31, 51 and 101 circular light spot and then scanned over the films by a galvanometric scanner through a long-focus objective or high-NA aspherical lens. These optical scheme and 5-μJ pulse energy supported the only 31- and 51-beam micro-patterning, with the corresponding aperture, field-of-view and sub-100 nJ energetic limitations for the laser processing of the film. The resulting large (~105–106 holes per array) arrays of micro-holes of variable diameters and periods in thin films of different thickness and diverse plasmonic materials - Ag, Cu, Al and Au-Pd alloy (80%/20%) - were for the first time systematically characterized in the broad IR-range (1.5–25 μm) in terms of plasmonic effects in extraordinary optical transmission, indicating for the increasing wavenumber a smooth transition from the common Bethe-Bouwkamp transmission to its plasmon-enhanced analogue, ending up with common geometrical (wave-guide-like) transmission. Finally, promising label- and luminescence-free laboratory-scale, robust and high-sensitivity sampling of chemicals and biosamples via plasmonic and chemical contributions, uneven and structurally-sensitive regarding different functional groups of the model analyte molecules and band structure of the plasmonic metal, was demonstrated for the large IR-sensing arrays of micro-holes in plasmonic films, with the obvious perspectives for down-scaling of sensing elements for vis-IR surface-enhanced spectroscopies.