Optical Detection of Ultrasound by Two-Wave Mixing in Photorefractive Semiconductor Crystals Under Applied Field

The optical detection of transient surface motion has many practical applications which include, in particular, the vibration monitoring of engineering structures (aircraft, power plants,...) and the detection of ultrasound produced by piezoelectric transducer or by pulse laser excitation. This last application where ultrasound is generated and detected by lasers, presents many advantages over conventional piezoelectric based methods. First, laser-ultrasonics is a remote sensing technique. Consequently it can be used, for example, for inspecting hot materials and products moving on a production line. Second, surfaces of complex shapes can also very easily be probed. For many applications, these advantages compensate the usually lower sensitivity of the laser-based technique compared to piezoelectric transduction

Near-infrared sensitivity enhancement of photorefractive polymer composites by pre-illumination

Among the various applications for reversible holographic storage media, a particularly interesting one is time-gated holographic imaging (TGHI). This technique could provide a noninvasive medical diagnosis tool, related to optical coherence tomography. In this technique, biological samples are illuminated within their transparency windowwith near-infrared light, and information about subsurface features is obtained by a detection method that distinguishes between reflected photons originating from a certain depth and those scattered from various depths. Such an application requires reversible holographic storage media with very high sensitivity in the near-infrared. Photorefractive materials, in particular certain amorphous organic systems, are in principle promising candidate media, but their sensitivity has so far been too low, mainly owing to their long response times in the near-infrared. Here we introduce an organic photorefractive material—a composite based on the poly(arylene vinylene) copolymer TPD-PPV—that exhibits favourable near-infrared characteristics. We show that pre-illumination of this material at a shorter wavelength before holographic recording improves the response time by a factor of 40. This process was found to be reversible. We demonstrate multiple holographic recording with this technique at video rate under practical conditions

Diffraction response of photorefractive polymers over nine orders of magnitude of pulse duration

The development of a single mode fiber-based pulsed laser with variable pulse duration, energy, and repetition rate has enabled the characterization of photorefractive polymer (PRP) in a previously inaccessible regime located between millisecond and microsecond single pulse illumination. With the addition of CW and nanosecond pulse lasers, four wave mixing measurements covering 9 orders of magnitudes in pulse duration are reported. Reciprocity failure of the diffraction efficiency according to the pulse duration for a constant energy density is observed and attributed to multiple excitation, transport and trapping events of the charge carriers. However, for pulses shorter than 30 μs, the efficiency reaches a plateau where an increase in energy density no longer affects the efficiency. This plateau is due to the saturation of the charge generation at high peak power given the limited number of sensitizer sites. The same behavior is observed in two different types of devices composed of the same material but with or without a buffer layer covering one electrode, which confirm the origin of these mechanisms. This new type of measurement is especially important to optimize PRP for applications using short pulse duration.AFOSR [FA9550-10-1-0207]; National Science Foundation through CIAN NSF ERC [EEC-0812072]; Office of Naval Research [N00014-14-1-0505]Open Access JournalThis item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at [email protected]