Generation of Violet and Blue Diffuse-Bands of Stimulated Radiation in Lithium Dimer

Blue(455.0-465.0 nm)and violet(407.0-418.0 nm)diffuse-bands of stimulated radiation are generated via two-photon excitation of lithium dimer by pumping laser tuned to any wavelength in the region of 620.0-660.0nm and via two-photon resonant excitation of atomic Li,respectively.The mechanisms involved are discussed.

The 3rd-order nonlinearity of bacteriorhodopsin by four-wave mixing

The 3rd-order nonlinear optical susceptibility x(3) and the response time of the light-transducing biomolecule bacteriorhodopsin were measured with the four-wave mixing technique and a picosecond frequency-doubled Nd: YAG laser (532 nm). The x(3) and the response time measured are 10-9 esu and 20 ps , respectively. The possible mechanism for generating the 3rd-order nonlinear optical susceptibility x(3) and response time were discussed.

Optical limiting of niobic tellurite glass induced by self-trapped exciton absorption of the AgCl nanocrystal dopant

Niobic tellurite glass doped by silver chloride nanocrystal was prepared with the melting-quenching and heat treatment method, and the self-trapped exciton absorption band of the silver chloride nanocrystal was observed at 532 nm in the UV-visible absorption spectrum. The glass structure characteristics were investigated by Raman spectroscopy, and the mechanism of self-trapped exciton was analyzed by Jahn-Teller model. Its optical limiting was measured with 532 nm picosecond laser pulses, and the corresponding nonlinear absorption coefficient was measured with open-aperture Z-scan. The experimental results showed that optical limiting at 532 nm was attributed to free carrier absorption between the self-trapped state and the continuum band.

Structural dependences of the η~6 complexes of 3-amino-9-ethylcarbazole with chromium tricarbonyl fragment on third-order optical nonlinearities

Degenerate four-wave mixing measurements, using the 35 ps pulses at 532 nm, have been employed to investigate the third-order nonlinear optical parameters of two chromium tricarbonyl complexes η6-bonded to 3-amino-9-ethylcarbazole at either the NH2-substituted aryl ring (1) or the unsubstituted ring (2) and their precursor 3-amino-9-ethylcarbazole (AECz). The second-order hyperpolarizability γ of the compounds 1 and 2 were found to be 42.9×10-31 and 35.9×10-31 esu, respectively, approximately one order of magnitude greater than AECz. The relation between the molecular structure and second-order hyperpolarizability of the compounds 1 and 2 was explored in detail based on the three-level model and the density functional theory (DFT) calculation. The theoretical results indicate that the spatial distri-bution of electron density has the profound role in the third-order nonlinear optical properties.

Linear and third-order nonlinear optical properties for the heptamethine cyanine chromophore H-aggregates thin film

The thin film of a heptamethine cyanine chromophore HC was prepared by spin-coating technique. Its surface morphology and linear optical property were characterized by atomic force microscopy (AFM) and UV-visible absorption spectroscopy. The results show that HC molecules are arranged in a well-ordered H-aggregate type. The third-order nonlinear optical properties of the spin-coating film were also measured by degenerate four-wave mixing (DFWM) measurement. Enhanced third-order nonlinear susceptibility can be attributed to molecular aggregation effects, and the corresponding mechanism was dealt with by collective electronic oscillator (CEO) approach.