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.
The optical and photoconductive fatigue of fast photorefractive polymers have been studied in a family of C 60-sensitized polymer composites containing styrene-based chromophores with varying ionization potential. Changes in response time and in photoconductivity were studied for exposures up to 10 4 J/cm 2. Increasing the chromophore ionization potential beyond that of the polyvinylcarbazole host was found to stabilize the response time. Studies of the electric-field dependence of the steady-state diffraction efficiency in various samples confirm the role of C 60 anions as possible traps.
This review describes the current state-of-the-art of photorefractive polymers for holography. The analysis of this rich field begins with a brief historical perspective followed by descriptions of prevailing physical models relating basic parameters of the polymer constituents to the bulk response of the final device. Methods for probing these responses and the underlying phenomena are discussed followed by an overview of the recent holographic applications of photorefractive polymers.
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.
We explore a novel, free-space optics based approach for building data center interconnects. It uses a digital micromirror device (DMD) and mirror assembly combination as a transmitter and a photodetector on top of the rack as a receiver (Figure 1). Our approach enables all pairs of racks to establish direct links, and we can reconfigure such links (i.e., connect different rack pairs) within 12 µs. To carry traffic from a source to a destination rack, transmitters and receivers in our interconnect can be dynamically linked in millions of ways. We develop topology construction and routing methods to exploit this flexibility, including a flow scheduling algorithm that is a constant factor approximation to the offline optimal solution. Experiments with a small prototype point to the feasibility of our approach. Simulations using realistic data center workloads show that, compared to the conventional folded-Clos interconnect, our approach can improve mean flow completion time by 30-95% and reduce cost by 25-40%.
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.
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