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Proceedings Paper

Experimental and numerical investigation of highly absorbing nonlinear organic chromophores
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Paper Abstract

We have developed a mathematical/numerical framework based on computational transition modules and measured ultrafast laser light propagating through nonlinear materials. The numerical framework can be applied to a broad set of photo-activated materials and lasers, and can optimize photo-physical parameters in multi-photon absorbers. Two photon (TPA) processes are particularly useful in many applications including fluorescence imaging, optical data storage, micro-fabrication, and nanostructured quantum dots for optical limiters. Laser transmission measurements of the organic molecular chromophore, AF455-known TPA material-were taken with a 175 fs, λ0=780nm, plane-polarized light pulses from Ti:S regenerative amplifier into a 5.1mm thick PMMA slab doped with the chromophore. The range of input energies (intensities) in this experiment was 0.01μJ (0.97 GW/cm2) to 25 μJ (2.4 x103 GW/cm2). Experiments showed that for intensities beyond several μJ, the material did not saturate as predicted by traditional theory. We included excited-state absorption (ESA), as demonstrated by the absorption spectrum, which still could not account for the deviation. To understand this result we used our framework to show that an unexpected/unknown higher energy level was being populated. We calculated the entire experimental curve from 0.01μJ (0.97 GW/cm2) to 25 μJ (2.4 x103 GW/cm2) and found excellent agreement with the experimental data.

Paper Details

Date Published: 15 February 2012
PDF: 15 pages
Proc. SPIE 8240, Nonlinear Frequency Generation and Conversion: Materials, Devices, and Applications XI, 82401N (15 February 2012); doi: 10.1117/12.909101
Show Author Affiliations
E. Parilov, Simphotek Inc. (United States)
M. J. Potasek, Simphotek Inc. (United States)
New York Univ. (United States)

Published in SPIE Proceedings Vol. 8240:
Nonlinear Frequency Generation and Conversion: Materials, Devices, and Applications XI
Konstantin L. Vodopyanov, Editor(s)

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