Browsing by Author "Jiang, Y."

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    Ultrafast nonlinear optical properties of dye-doped PMMA discs irradiated by 40 fs laser pulses
    (2009) Xia, Y.; Jiang, Y.; Fan, R.; Dong, Z.; Zhao, W.; Chen, D.; Umesh, G.
    The two-photon absorption (TPA) characteristics of PMMA discs doped with three different dyes were studied using an fs-pulsed Ti-Sapphire laser as the pump source, and employing the open-aperture Z-scan technique. TPA cross-sections obtained for PMMA doped with the dyes PM597, DCM and rhodamine 6G-rhodamine B (co-doped) were found to be equal to 24.7, 33.3 and 32.3 GM, respectively (1 GM=10-50 cm4 s phot-1 mol-1). Furthermore, two-photon fluorescence was measured for the samples containing DCM and rhodamine 6G-rhodamine B (co-doped). Compared to the one-photon fluorescence spectrum, the peaks in the two-photon fluorescence spectrum were red shifted and the extent of red shift increased with increasing doping concentration. We have also observed that the red shift in the two-photon fluorescence peak of the samples in the solid form is much larger than that in the solution state. This phenomenon could be explained by a twisted intra-molecular charge transfer model. � 2009 Elsevier Ltd. All rights reserved.
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    Ultrafast nonlinear optical properties of dye-doped PMMA discs irradiated by 40 fs laser pulses
    (2009) Xia, Y.; Jiang, Y.; Fan, R.; Dong, Z.; Zhao, W.; Chen, D.; Umesh, G.
    The two-photon absorption (TPA) characteristics of PMMA discs doped with three different dyes were studied using an fs-pulsed Ti-Sapphire laser as the pump source, and employing the open-aperture Z-scan technique. TPA cross-sections obtained for PMMA doped with the dyes PM597, DCM and rhodamine 6G-rhodamine B (co-doped) were found to be equal to 24.7, 33.3 and 32.3 GM, respectively (1 GM=10-50 cm4 s phot-1 mol-1). Furthermore, two-photon fluorescence was measured for the samples containing DCM and rhodamine 6G-rhodamine B (co-doped). Compared to the one-photon fluorescence spectrum, the peaks in the two-photon fluorescence spectrum were red shifted and the extent of red shift increased with increasing doping concentration. We have also observed that the red shift in the two-photon fluorescence peak of the samples in the solid form is much larger than that in the solution state. This phenomenon could be explained by a twisted intra-molecular charge transfer model. © 2009 Elsevier Ltd. All rights reserved.