Self-reconstructing all-optical poling in polymer fibers.

Self-sustained all-optical poling second-harmonic generation (SHG) experiments are conducted in single-core and multicore dye-doped poly(methyl methacrylate) optical fibers. By tuning the polarization of the fundamental beam, the SHG signal is degraded and is reconstructed spontaneously up to its initial level. We found a new situation in which the photo-induced self-organization of azo polymers creates a well-ordered periodic structure.

Stable frequency doubling by all-optical poling in dye-doped polymer optical fibers.

We present experimental studies of all-optical poling (AOP) in large-core dye-doped poly(methyl methacrylate) plastic optical fibers. We show that the confinement of light within the fiber core permits us to reach the upper limit of second harmonic generation achievable by AOP using repeated trans-cis isomerization. Quantification of the output power indicates self-seeding that can counteract relaxation of the orientation during readout of the induced nonlinearity.

Combining very large quadratic and cubic nonlinear optical responses in extended, tris-chelate metallochromophores with six pi-conjugated pyridinium substituents.

We describe a series of nine new complex salts in which electron-rich Ru(II) or Fe(II) centers are connected via pi-conjugated bridges to six electron-accepting N-methyl-/N-arylpyridinium groups. This work builds upon our previous preliminary studies (Coe , B. J.

Bridged triphenylamine-based dendrimers: tuning enhanced two-photon absorption performance with locked molecular planarity.

Triphenylamine derivatives bridged by methylene units afford a near planar molecular platform in a series of one dimer and two oligomers exhibiting increased structural rigidity compared to that of their parent triphenylamines. This series of dendrimers show significantly enhanced two-photon absorptions that are up to 3-fold that of triphenylamines with similar molecular size and structure.

Two-photon absorption properties of iron(II) and ruthenium(II) trischelate complexes of 2,2':4,4' ':4',4' ''-quaterpyridinium ligands.

A series of RuII or FeII trischelate complex salts containing N-methyl/aryl-2,2':4,4' ':4',4' ''-quaterpyridinium ligands that has previously been subjected to quadratic nonlinear optical studies (Coe, B. J. et al.

Third harmonic autocorrelation and wave mixing in a thin film of poly(p-phenylenevinylene).

We show here that a thin film of a nonlinear conjugated polymer: poly(p-phenylenevinylene) (PPV) is capable of efficiently generating the third harmonic of femtosecond pulses of light at the near infrared (including telecommunication bands) wavelengths, giving coherent, low divergence beams in the visible range. By using more than one fundamental beam overlapping in space and in time on the PPV film, autocorrelation signals are observed as well as higher order mixing signals due to X(5) and higherorder nonlinear susceptibilities. These signals can be used for applications such as short laser pulse diagnostics and photonic signal processing and they provide information about the nonlinear properties of the material itself.