Loic Mager

High net gain at 514 nm in a photorefractive polymer doped with a chalcone derivative

We report on the photorefractive properties of a low Tg composite consisting of functionalized polysiloxane doped with a chalcone derivative. The high transparency of this doping molecule enabled the observation of high net gain at 514 nm. Orientational and Pockels contributions to the total refractive index variations were measured by frequency-dependent ellipsometry experiments. Finally, the field dependence of the gain coefficient is described using Kukhtarev’s model for the space charge field with an effective trap density as a single fitting parameter.

New layered organic-inorganic magnets incorporating azo dyes

New hybrid organic/inorganic magnets have been synthesized by insertion of stilbazolium-carboxylate and/or -sulfonate dyes into cobalt and copper layered hydroxides. Co2(OH)3.57(MR)0.43·1.88 H2O (MR⊂Co (1)) (MRNa: Methyl Red sodium salt: sodium 2-[4-(Dimethylamino)phenylazo]benzoate), Co2(OH)3.27(MO)0.73·2.94 H2O (MO⊂Co (2)) (MONa: Methyl Orange sodium salt: sodium 4-[4-(Dimethylamino)phenylazo]benzenesulfonate), Co2(OH)3.45(OrangeIV)0.55·2.92 H2O (OrangeIV⊂Co (3)) (OrangeIVNa: OrangeIV sodium salt: sodium 4-[4-(Anilino)phenylazo]benzenesulfonate), and Co2(OH)3.46(MY10)0.27·2.34 H2O (MY10⊂Co (4)) (MY10Na2: Mordant Yellow 10 disodium salt: sodium 3-[4-(sodium sulfonate)phenylazo]-6-hydroxybenzoate) have been synthesized by anionic exchange in alkaline media starting from Co2(OH)3(OAc)·H2O. Cu2(OH)3.23(MR)0.77·2.92 H2O (MR⊂Cu (5)), Cu2(OH)3.29(MO)0.71·2.31 H2O (MO⊂Cu (6)), and Cu2(OH)3.39(OrangeIV)0.61·1.80 H2O (OrangeIV⊂Cu (7)) were obtained starting from the pre-intercalated copper hydroxide Cu2(OH)3(DS) (DS−: dodecylsulfate). This is the first time pre-intercalation is used for the insertion of molecules within the interlamellar space of simple layered hydroxides. The hybrid copper layered hydroxides show ferrimagnetic behaviour with ordering at very low temperature (below 1.8 K). The cobalt analogues are ferrimagnets with ordering temperatures ranging from 6.9 K to 18 K.

Polarization state studies in second harmonic generation signals to trace atherosclerosis lesions

We have performed multi-photon image reconstructions as well as polarization state analyses inside an artery wall affected by atherosclerosis to investigate the changes in collagen structure. Mice, either healthy or affected by spontaneous atherosclerosis, have been used for this purpose. A two-photon imaging system has been used to investigate atherosclerotic lesions in the ascending aorta of mice. Second harmonic imaging has been performed alternatively on healthy samples and on affected region. The reconstructed images show that the spatial distribution of the collagen network seems disorganized by the disease. The polarization state studies reveal however that the apparent disorganization of the collagen is related to its spatially diffuse distribution and that the internal structure of the collagen fibers is not affected by the disease. In addition, a theoretical simulation of the second harmonic polarization states shows that they are consistent with the known 3D structure of the collagen network.

Solvent-free fluidic organic dye lasers

We report on the demonstration of liquid organic dye lasers based on 9-(2-ethylhexyl)carbazole (EHCz), so-called liquid carbazole, doped with green- and red-emitting laser dyes. Both waveguide and Fabry-Perot type microcavity fluidic organic dye lasers were prepared by capillary action under solvent-free conditions. Cascade Förster-type energy transfer processes from liquid carbazole to laser dyes were employed to achieve color-variable amplified spontaneous emission and lasing. Overall, this study provides the first step towards the development of solvent-free fluidic organic semiconducting lasers and demonstrates a new kind of optoelectronic applications for liquid organic semiconductors.

Electronic energy and electron transfer processes in photoexcited donor-acceptor dyad and triad molecular systems based on triphenylene and perylene diimide units.

We investigate the photophysical properties of organic donor-acceptor dyad and triad molecular systems based on triphenylene and perylene diimide units linked by a non-conjugated flexible bridge in solution using complementary optical spectroscopy techniques. When these molecules are diluted in dichloromethane solution, energy transfer from the triphenylene to the perylene diimide excited moieties is evidenced by time-resolved fluorescence measurements resulting in a quenching of the emission from the triphenylene moieties. Simultaneously, another quenching process that affects the emission from both donor and acceptor units is observed. Solution ultrafast transient absorption measurements provide evidence of photo-induced charge transfer from either the donor or the acceptor depending upon the excitation. Overall, the analysis of the detailed time-resolved spectroscopic measurements carried out in the dyad and triad systems as well as in the triphenylene and perylene diimide units alone provides useful information both to better understand the relations between energy and charge transfer processes with molecular structures, and for the design of future functional dyad and triad architectures based on donor and acceptor moieties for organic optoelectronic applications.

Toward submicrometer optical storage through controlled molecular disorder in azo-dye copolymer films

While information encoding through optically induced orientation of azo dyes in organic matrices is being extensively pursued, we propose the alternative of starting out with poled films and to locally reduce their second-harmonic generation capacity by a focused near-infrared femtosecond laser beam of moderate intensity. Arrays of dots irradiated under varying conditions are subsequently imaged in situ as dark spots on a bright background. The samples are also examined through conventional optical microscopy and through atomic force microscopy. We demonstrate that, of these techniques, second-harmonic imaging performs best in the task of information retrieval.

Low threshold amplified spontaneous emission and ambipolar charge transport in non-volatile liquid fluorene derivatives

Highly fluorescent non-volatile fluidic fluorene derivatives functionalized with siloxane chains were synthesized and used in monolithic solvent-free liquid organic semiconductor distributed feedback lasers. The photoluminescence quantum yield values, the amplified spontaneous emission thresholds and the ambipolar charge carrier mobilities demonstrate that this class of materials is extremely promising for organic fluidic light-emitting and lasing devices.

Structure–charge transfer property relationship in self-assembled discotic liquid-crystalline donor–acceptor dyad and triad thin films

The photophysical properties of donor–acceptor (D–A) and donor–acceptor–donor (D–A–D) liquid crystalline dyads and triads based on two different discotic mesogens are examined in thin films by steady-state optical spectroscopy and subpicosecond transient absorption measurements. In these systems, triphenylene and perylene bisimide units are covalently linked by flexible decyloxy chain(s) and act as an electron donor (D) and acceptor (A), respectively. These discotic liquid-crystalline systems form well-separated D and A π-stacked columnar structures in thin films. The absorption spectra of the films indicate an aggregation of the perylene bisimide and triphenylene moieties along the columns. Steady-state photoluminescence measurements show a strong fluorescence quenching that is mainly attributed to a photo-induced charge transfer process taking place between the triphenylene and perylene bisimide units. Subpicosecond transient absorption measurements show that the photoinduced charge transfer (CT) states in the dyad and triad films are formed within 0.3 ps and recombine on a 150–360 ps time scale. In addition, a correlation between the dynamics of the charge recombination process and the spacing distances between D and A units can be established in the dyad and triad films. This study provides important information on the relationship between molecular packing and the charge transfer properties in such self-organized D and A columnar nanostructures.

Light induced self-written waveguides interactions in photopolymer media.

We present experimental and theoretical study of the interaction of Light Induced Self-Written (LISW) waveguides in photopolymers. We show that the diffusion of the monomer controls the refractive index distribution. Consequently it influences the interaction between the LISW channels allowing the observation of anti-crossing behavior or the propagation of an array of non interacting LISW waveguides.

Near infrared two-photon self-confinement in photopolymers for light induced self-written waveguides fabrication

We present the fabrication of single mode light induced self-written waveguides using two-photon absorption in photopolymers. The measurements are compared to the finite element method simulation of the propagation and demonstrate that two-photon process leads to the confinement of light.