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Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE

Picosecond Time- And Space-Domain Holography By Photochemical Hole Burning

Peeter Saari, Rein K. Kaarli, Alexander Rebane

Published Jan 15, 1988• 0 citations
Publisher

Abstract

In this paper, the concept of holographic storage and reproduction of optical signals is generalized for the case of a spectrally highly selective recording medium, which in addition to fixing the spatial intensity distribution of the incident light is also able to memorize its intensity spectrum. We demonstrate persistent storage, recall and conjugation of picosecond light signals from various model objects by making use of coherent optical responses in photochemically active media. A simple linear theory of holographic storage and playback of both the spatial and the temporal behaviour of the signal is shown to well describe the experimental results obtained by utilizing octaethylporphin-doped polystyrene at 1.8 K as a spectrally selective recording material. The proposed method of time- and space-domain holographic recording provides the storage and reproduction of time-dependent optical signals with a duration of 10-8 to 10-13 sec. This presents unique possibilities for ultrahigh-speed data-storage and optical signal-processing.

DOI
10.1117/12.939033

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In this paper, the concept of holographic storage and reproduction of optical signals is generalized for the case of a spectrally highly selective recording medium, which in addition to fixing the spatial intensity distribution of the incident light is also able to memorize its intensity spectrum. We demonstrate persistent storage, recall and conjugation of picosecond light signals from various model objects by making use of coherent optical responses in photochemically active media. A simple linear theory of holographic storage and playback of both the spatial and the temporal behaviour of the signal is shown to well describe the experimental results obtained by utilizing octaethylporphin-doped polystyrene at 1.8 K as a spectrally selective recording material. The proposed method of time- and space-domain holographic recording provides the storage and reproduction of time-dependent optical signals with a duration of 10-8 to 10-13 sec. This presents unique possibilities for ultrahigh-speed data-storage and optical signal-processing.
Time-and-space-domain holography [1,2] can be regarded as an extension of a conventional holographic process, where, in addition to the spatial image, the hologram plays back the time dependence of an event. The play-back of events is possible because we are using highly frequency-selective inhomogeneously broadened absorbers as recording material. This technique has a variety of potential applications in optical data storage and processing. In the present paper we consider the basic physical principle of time-and-space-domain storage in frequency-selective materials which exploit the effect of spectral hole burning [3]. In particular we will show that organic dye-doped spectral hole burning materials allow recording and playback of pi- co- and femtosecond time-scale events.
Spectral hole burning media — photochemically i9stable dye molecules in low—temperature polymers hibit very narrow (10 Hz) optical resonances distributed over a wide (10 Hz) band along the frequency axis. Exposure of the medium to recording light field burns a 4—D grating pattern into the dielectric permittivity tensor c(x,y,z,), which in turn determines the temporal behaviour of the linear pulse response of the sample. Based on this phenomenon the common holography has been generalized resulting in a 4—D holography where restored light field is completely identical to the stored one and plays back ultrafast temporal behaviour of the object light as pulsed vector field. In the paper, the approach is extended for applications listed in the title and corresponding experimental results of streak —camera measurements on octaethyl—porphin —doped polystyrene plates are briefly discussed.
Time-and-space-domain holography [1,2] by stimulated photon echoes [3] provides a means of storing temporal and spatial properties of an ultrafast-varying light signal and recalling its authentic replica at any later moment. The possibility of recording complex time shapes of light pulses, which also means time-domain optical data storage, is based on the ability of frequency-selective absorbers to store with high accuracy the temporal Fourier components of the incident light [1-3]. The time-domain frequency-selective optical storage of binary or analog data is an alternative approach to the concept of frequency-selective high-density data storage that provides a parallel ultrafast data storage and processing in the frequency domain. The shortest detail of the signal to be stored is limited by the reverse inhomogeneous bandwidth of the storing media which reaches 10-100 fs for frequency-selective materials while the duration of the signal is limited by phase relaxation time T2 (usually 10-3-10-6s).
Persistent spectral hole burning (PSHB) in organic molecules doped in a polymer matrix at low temperatures allows optical recording of information in the dimensions of frequency and time, as well as in space and externally applied electric field. We use this special property to demonstrate new types of holograms, which extend conventional spatial-domain optical data storage into the new dimensions. Basic aspects of recording and playback of holograms by persistent spectral hole burning, including relation between frequency- and time-domain response function, is discussed. This paper is elucidating inherent relations between the time- and frequency-domain versions of PSHB holography. We show that by multiplexing holograms in the frequency dimension, we can store a large number (up to 12 000) of image holograms using a single spectral hole burning sample. In the time domain, we show storage and reproduction of ultrashort time-space images on the scale of 10 -12 −10 -13 s. Experiments demonstrating unusual hologram properties, such as causality-related asymmetry of diffraction, inversion of time coordinate, and ultrafast processing, are presented.