Achieving enhanced gain in photorefractive polymers by eliminating electron contributions using large bias fields.

Photorefractive polymers have been extensively studied for over two decades and have found applications in holographic displays and optical image processing. The complexity of these materials arises from multiple charge contributions, for example, leading to the formation of competing photorefractive gratings. It has been recently shown that in a photorefractive polymer at relatively moderate applied electric fields the primary charge carriers (holes) establish an initial grating, followed by a subsequent competing grating (electrons) resulting in a decreased two-beam coupling and diffraction efficiencies. In this paper, it is shown that with relatively large sustainable bias fields, the two-beam coupling efficiency is enhanced owing to a decreased electron contribution. These results also explain the cause of dielectric breakdown experienced under large bias fields. Our conclusions are supported by self-pumped transient two-beam coupling and photocurrent measurements as a function of applied bias fields at different wavelengths.

Interdigitated coplanar electrodes for enhanced sensitivity in a photorefractive polymer.

Organic photorefractive polymer composites can be made to exhibit near 100% diffraction efficiency and fast writing times, though large external slants are needed to project the applied field onto the grating vector. We show here that the use of interdigitated electrodes on a single plane provides similar performance to these standard devices and geometries but without a external slant angle. This new device's structure also greatly improves the diffraction efficiency and sensitivity compared to less slanted standard devices necessary for some real applications, such as holographic displays, optical coherence imaging, and in-plane switching.

Holographic three-dimensional telepresence using large-area photorefractive polymer.

Holography is a technique that is used to display objects or scenes in three dimensions. Such three-dimensional (3D) images, or holograms, can be seen with the unassisted eye and are very similar to how humans see the actual environment surrounding them. The concept of 3D telepresence, a real-time dynamic hologram depicting a scene occurring in a different location, has attracted considerable public interest since it was depicted in the original Star Wars film in 1977. However, the lack of sufficient computational power to produce realistic computer-generated holograms and the absence of large-area and dynamically updatable holographic recording media have prevented realization of the concept. Here we use a holographic stereographic technique and a photorefractive polymer material as the recording medium to demonstrate a holographic display that can refresh images every two seconds. A 50 Hz nanosecond pulsed laser is used to write the holographic pixels. Multicoloured holographic 3D images are produced by using angular multiplexing, and the full parallax display employs spatial multiplexing. 3D telepresence is demonstrated by taking multiple images from one location and transmitting the information via Ethernet to another location where the hologram is printed with the quasi-real-time dynamic 3D display. Further improvements could bring applications in telemedicine, prototyping, advertising, updatable 3D maps and entertainment.

Grating dynamics in a photorefractive polymer with Alq(3) electron traps.

The electron transporting molecule tris(8-hydroxyquinoline) aluminum (Alq(3)) was added in low concentrations to a photorefractive polymer composite to provide trapping sites for electrons. This sample exhibited larger two-beam coupling gain, higher diffraction efficiency at lower voltages, and an increased dielectric breakdown strength compared to a control sample. The dynamics also revealed the presence of a competing grating, and a bipolar charge transport model is shown to fit the data. Overall, Alq(3) improves the response time, efficiency, and breakdown voltage without a significant increase in absorption or loss of phase stability. This has applications for reflection displays and pulsed writing, where charge trapping and generation are major factors limiting the usefulness of photorefractive polymers.

An updatable holographic three-dimensional display.

Holographic three-dimensional (3D) displays provide realistic images without the need for special eyewear, making them valuable tools for applications that require situational awareness, such as medical, industrial and military imaging. Currently commercially available holographic 3D displays use photopolymers that lack image-updating capability, resulting in restricted use and high cost. Photorefractive polymers are dynamic holographic recording materials that allow updating of images and have a wide range of applications, including optical correlation, imaging through scattering media and optical communication. To be suitable for 3D displays, photorefractive polymers need to have nearly 100% diffraction efficiency, fast writing time, hours of image persistence, rapid erasure, and large area-a combination of properties that has not been shown before. Here, we report an updatable holographic 3D display based on photorefractive polymers with such properties, capable of recording and displaying new images every few minutes. This is the largest photorefractive 3D display to date (4 x 4 inches in size); it can be recorded within a few minutes, viewed for several hours without the need for refreshing, and can be completely erased and updated with new images when desired.

Variation of Bragg condition in low-glass-transition photorefractive polymers when recorded in reflection geometry.

Two low-glass transition photorefractive polymer composites were investigated in a symmetric reflection geometry. The holograms recorded in 105 mum thick devices have reached diffraction efficiencies as high as 60%. Unlike the gratings recorded in transmission geometry, holograms recorded in reflection geometry showed high angular selectivity and the Bragg condition was observed to be sensitive to the magnitude of the external bias field. We attribute this effect to poling-induced birefringence and give a theoretical analysis to describe the observed results.

Photorefractive polymers sensitized by two-photon absorption.

We demonstrate the recording of holograms and their nondestructive readout in a photorefractive polymer, using two-photon absorption. Sensitivity is provided by the excitation of the electroactive chromophore with femtosecond pulses, followed by charge injection into the photoconducting poly(N -vinylcarbazole) matrix. The holograms can be fully erased with a pulsed laser source but are insensitive to cw laser beams with the same wavelength. Studies of the field and intensity dependence of the diffraction efficiency indicate that the holograms are formed through the photorefractive effect.

Evidence for intervalence band coherences in semiconductor quantum wells via coherently coupled optical Stark shifts.

We report the experimental observation of coherently coupled heavy-hole-light-hole Stark shifts, i.e., light-hole exciton shifts under heavy-hole exciton pumping conditions, in InGaAs quantum wells. The theoretical analysis of the data is based on a full many-body approach (dynamics-controlled truncation formalism) in the third-order nonlinear optical regime. It is shown that the Stark shift data can be interpreted as strong evidence of suitably defined nonradiative intervalence band coherences in a semiconductor quantum well. Hence, the observations establish a semiconductor analog of Raman coherences in three-level atoms.

Two-photon resonant third-harmonic generation in La2CuO4.

Combining linear absorption and nonlinear third harmonic generation (THG) experiments, we investigate details of the electronic structure of the highly correlated electronic system in La2CuO4. We demonstrate strong THG mainly due to the charge transfer excitation from O (2p(sigma)) to Cu (3d(x2-y2)). The THG spectrum shows pronounced features due to three-photon and two-photon resonance enhancement as well as quantum interference effects. We obtain excellent agreement with a THG spectrum calculated in terms of the excitonic cluster model and can identify both odd and even symmetry excitation modes.

Photoinduced orientation of azo dye in various polymer matrices.

Photoinduced dichroism in various polymers containing the same azo dye has been studied. "Angular hole burning" and molecular reorientation have been identified by analysis of dichroism dynamics at various probe wavelengths. The glass-transition temperature T(g) is of major relevance for the reorientation of optically active molecules. For low T(g) (below ambient temperature) thermal diffusion impedes anisotropy buildup. For higher T(g) the angular distribution induced by the polarized pump beam is frozen. We propose a simple model based on diffusion rates in trans and cis molecules.