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Chemical Physics

Power broadening of the spectral hole width in an optically thick sample

Eric S. Maniloff, Felix R. Graf, Hansruedi Gygax, Stefan B. Altner, Stefan Bernet, Alois Renn, Urs P. Wild

Published Apr 1, 1995• 15 citations
Publisher
DOI
10.1016/0301-0104(94)00417-9

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One very exciting application of laser spectroscopy would be to use the high-resolution capabilities of today’s lasers and the phenomenon of persistent spectral hole-burning to form a frequency domain optical storage system.1 In such a system, bits of information would be stored by locally modifying (in the frequency domain) the shape of an inhomogeneously broadened absorption line of an absorber in a solid at low temperatures. Because typical homogeneous widths are 1000X (or more) narrower than typical inhomogeneous widths, as many as 1000 bits could be written in one diffraction-limited 1-μm spot In a sample, yielding the impressive storage density of 1011 bits/cm2.

Conference on Lasers and Electro-Optics•Jan 1, 1983•1 citation
Optical hole burning is used to study optical dephasing of the 7F0 ⇒ 5D0 transition in samples of Y2O3:Eu3+ grown by both flame fusion and laser-heated pedestal growth. The samples exhibited a wide variation in their low-temperature hole widths, and the measured hole linewidths were in reasonable agreement with homogeneous linewidths obtained from values of T2 that were determined with two-pulse photon echoes. The sample that had the longest value of T2 (510 μs) from the echo measurements gave a hole width of 3.5 kHz. This is believed to be the narrowest spectral feature observed directly in the frequency domain for a solid. Other samples produced wider holes that were not correlated with the Eu3+ impurity concentrations. Time-resolved hole burning in one of the samples showed a slow and continuous broadening of the spectral hole from 130 kHz at 3 ms to 900 kHz at 10 s after hole burning. It is suggested that the additional broadening is associated with some form of disorder modes in this ordered crystalline solid.
Photochemical spectral hole-burning (PSHB) has attracted particular attention in the past decade because of its potential for frequency domain optical storage. In order to apply PSHB to a practical optical memory, the material should have high burning temperature, high thermal stability, erasability and high frequency multiplexing. Two ways are possible to increase the storage density: one is to narrow the homogeneous line width, the other is to broaden the inhomogeneous line width. In previous works, the larger inhomogeneous line width (greater than 1,000 cm–1) has been reached in polymethylmethacrylate (PMMA) doped with two kinds of Zn-benzoporphyrin derivatives with roughly the same hole-burning efficiencies [1]. In this paper, the authors investigate systematically the optical properties of Zn-benzoporphyrin derivatives, their hole-burning mechanisms, thermal stability and electron-phonon coupling in cellulose acetate (CA) and in PMMA matrices. The choice of CA was motivated mainly by the fact this polymer allows to prepare samples with excellent optical quality.
One very exciting application of laser spectroscopy would be to use the high-resolution capabilities of today’s lasers and the phenomenon of persistent spectral hole-burning to form a frequency domain optical storage system.1 In such a system, bits of information would be stored by locally modifying (in the frequency domain) the shape of an inhomogeneously broadened absorption line of an absorber in a solid at low temperatures. Because typical homogeneous widths are 1000X (or more) narrower than typical inhomogeneous widths, as many as 1000 bits could be written in one diffraction-limited 1-μm spot In a sample, yielding the impressive storage density of 1011 bits/cm2.