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Nonphotochemical hole burning of laser dyes, rare earth ions and photosynthetic pigments in polymer films

Thomas P. Carter

Published Jan 1, 1986• 0 citations
Publisher

Abstract

The results of nonphotochemical hole burning (NPHB) and laser induced hole filling (LIHF) experiments are reported for several impurities intentionally doped into thin polymer films. The polymer films provide an amorphous environment for the dopants which can be easily and reproducibly prepared at room temperature, and they are convenient in handling since they are solids at ordinary temperatures. Thus, polymer films have several advantages over the various low temperature glasses which have been used previously for NPHB studies. The systems studied include the polymers poly(vinyl alcohol) and poly(acrylic acid) doped with various organic ionic dyes (cresyl violet, rhodamine 560 and 640, nile blue, and oxazine 720 and 725, all of which are used as the active gain medium in dye lasers) as well as the rare earth ions Pr('3+) and Nd('3+). Additionally, polystyrene was used as the amorphous host in NPHB and LIHF studies of chlorophyll a, chlorophyll b and self-aggregated dimers of chlorophyll a;The NPHB of the ionic dyes is efficient, and the spectra exhibit extensive intramolecular vibronic satellite holes which provide accurate S(,1) vibronic frequencies for the dopant. The homogeneous linewidths of the impurity S(,0) (--->) S(,1) transitions inferred from measured hole widths yields dephasing rates which are one to two orders of magnitude faster than observed in crystals and "hard" inorganic glasses (silica e.g.), and is taken as evidence for rapid pure dephasing processes occurring in the polymer systems even at 1.8 K. The LIHF of these systems is also efficient and shows a pronounced change in efficiency when the relative magnitudes of the laser frequencies for the first and second irradiations is reversed. Also, the efficiency of LIHF is insensitive to the amount of radiation absorbed by the dopant, and hence shows little change as the secondary burn frequency is moved relative to the primary frequency (except as noted above). This same LIHF behavior was observed in all the systems reported herein and may have profound implications as to the structure of glassy media;The chlorophyll systems also show efficient NPHB but no intramolecular vibronic holes are observed. These systems also show evidence of rapid pure dephasing processes even at 1.8 K. The results obtained for the monomer chlorophyll NPHB are used to help interpret the results obtained for the self-aggregated dimers which, in turn, were obtained to help in the interpretation of planned future experiments on chlorophylls in in vivo environments;Finally, a brief review of relevant NPHB research and the various theories used to describe the hole burning process is presented.

DOI
10.31274/rtd-180813-5717

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Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE•Aug 13, 1993•0 citations
The results of nonphotochemical hole burning (NPHB) and laser induced hole filling (LIHF) experiments are reported for several impurities intentionally doped into thin polymer films. The polymer films provide an amorphous environment for the dopants which can be easily and reproducibly prepared at room temperature, and they are convenient in handling since they are solids at ordinary temperatures. Thus, polymer films have several advantages over the various low temperature glasses which have been used previously for NPHB studies. The systems studied include the polymers poly(vinyl alcohol) and poly(acrylic acid) doped with various organic ionic dyes (cresyl violet, rhodamine 560 and 640, nile blue, and oxazine 720 and 725, all of which are used as the active gain medium in dye lasers) as well as the rare earth ions Pr('3+) and Nd('3+). Additionally, polystyrene was used as the amorphous host in NPHB and LIHF studies of chlorophyll a, chlorophyll b and self-aggregated dimers of chlorophyll a;The NPHB of the ionic dyes is efficient, and the spectra exhibit extensive intramolecular vibronic satellite holes which provide accurate S(,1) vibronic frequencies for the dopant. The homogeneous linewidths of the impurity S(,0) (--->) S(,1) transitions inferred from measured hole widths yields dephasing rates which are one to two orders of magnitude faster than observed in crystals and "hard" inorganic glasses (silica e.g.), and is taken as evidence for rapid pure dephasing processes occurring in the polymer systems even at 1.8 K. The LIHF of these systems is also efficient and shows a pronounced change in efficiency when the relative magnitudes of the laser frequencies for the first and second irradiations is reversed. Also, the efficiency of LIHF is insensitive to the amount of radiation absorbed by the dopant, and hence shows little change as the secondary burn frequency is moved relative to the primary frequency (except as noted above). This same LIHF behavior was observed in all the systems reported herein and may have profound implications as to the structure of glassy media;The chlorophyll systems also show efficient NPHB but no intramolecular vibronic holes are observed. These systems also show evidence of rapid pure dephasing processes even at 1.8 K. The results obtained for the monomer chlorophyll NPHB are used to help interpret the results obtained for the self-aggregated dimers which, in turn, were obtained to help in the interpretation of planned future experiments on chlorophylls in in vivo environments;Finally, a brief review of relevant NPHB research and the various theories used to describe the hole burning process is presented.
Permanent and transient hole-burning experiments carried out on various types of amorphous systems at temperatures between 0.3 and 20 K are presented. Optical dephasing on organic molecules in glasses and polymers measured on different time scales are discussed in relation to spectral diffusion processes and compared to the literature. The pure dephasing time appears to be proportional to the excited state lifetime of the guest. Organic molecules adsorbed on the surface of porous silica glass show that their homogeneous linewidth is an order of magnitude larger than in polymers and glasses in the bulk, but follows the same temperature dependence. Hole-burning results on bacteriochlorophyll in various disordered hosts are compared to those on a isolated light-harvesting photosynthetic pigment-protein complex (B800–850). From the holewidth in the latter the energy transfer rate between aggregated bacteriochlorophyll pigments is determined and compared to time-resolved spectroscopy results in the literature.
Laser induced hole burning in optical absorption bands of low temperature solids has been investigated with emphasis on mechanisms for population hole burning, the interactions with the environment which limit the hole widths and the use of hole burning for ultra high resolution spectroscopy. Hole burning was observed in a wide range of solids including organic and organometallic molecules in crystals and rare earth ions in crystals and glasses. The mechanisms for hole burning also varied widely and a new mechanism involving optically induced nuclear spin flips of near neighbor nuclei was discovered. Examples of hole burning in new classes of materials are presented here for the first time, namely inorganic glasses (silicate glasses containing Nd(3+), Pr(3+) or Eu(3+)) and undoped stoichiometric compounds (e.g., EuP5O14). Hole recovery was used to determine nuclear spin lattice relaxation rates in praseodymium doped crystals. For allowed optical transitions (e.g., singlet states of zinc porphyrin, dibromoindigo and color centers in alkali halides) the hole widths at 2K are limited by population decay to approximately 50 MHz. For longer lived optical levels in crystalline materials, e.g., those containing rare earth ions, the hole widths are narrower (less than 10 MHz) and are limited by dynamical interactions with surrounding nuclei. In amorphous materials such as europium doped silicate glass, hole widths are much broader, being limited by low frequency tunneling motions. Hole burning measurements were complemented by time domain coherent transient (photon echo, and optical free decay) measurements of homogeneous linewidths which enabled us to measure optical resonances as narrow as 760 Hz in Eu(3+):Y2O3.
The persistent spectral hole-burning (PSHB) phenomenon has been known since 1974. It is still an important research area for the study of the intimacy of complex molecular systems in the solid state, revealing high-resolution spectra, photophysics, photochemistry, and dynamics of molecular doped amorphous media, organic as well as inorganic. From another point of view, PSHB allows the engraving of any spectral structures in the inhomogeneous absorption band profile of molecular doped amorphous hosts or ion doped crystals cooled down to liquid helium temperatures. Therefore, a PSHB material is programmable in the spectral domain and consequently it can be transformed in an optical processor capable of achieving user-defined optical functions. Some aspects of both fields are illustrated in the present paper. Concerning the search for efficient PSHB materials, the hole-burning performances and the photophysics of polymer and xerogel based systems are compared. The problem of high-temperature persistent spectral hole-burning materials and the search for new frequency selective photosensitive systems for fast optical pulse processing at 800nm are considered. Regarding the points treated, inorganic hosts based on silicate xerogels or porous glasses have shown the best results. Moreover, by combining inorganic and organic capabilities or by grafting organic species to the host, hybrid xerogels have not yet revealed all possibilities. Also, the interest of two-photon materials for engraving spectral features with near-infrared or infrared light is developed. As an introduction to possible applications of PSHB material, the basics of spectro-temporal holography are remembered and a demonstrative experiment using a naphthalocyanine-doped polymer film is described, proving that the temporal aberration free recompression of ultrashort light pulses is feasible, therefore opening a way for applications in ultrashort light pulse shaping. Aspects for a comparison between cw hole-burning and femtosecond spectro-temporal experiments are considered, and prospects for coherent control of light fields or photochemical processes are also evoked.
Recently, the interests in optical memory based on persistent spectral hole burning (PSHB) are increased because of its possibility of the application to high density optical memory. PSHB was observed for an organic dye doped in polymer and rear earth or transition metal doped in inorganic crystal or glasses up to now. Since PSHB was observed by two Russian groups (Gorokhovskii et al. and Kharlamov et al.) for free base phthalocyanine in a n-octane Shpol'skii matrix1 and for perylene and 9-aminoacridine molecules in glassy ethanol matrix2, PSHB materials are studied primarily for the polymer doped with an organic dye. But such materials can make hole only at very low temperature. Room temperature PSHB phenomena were observed on Sm2+ doped fluoride crystals3-5 and glasses6 recently, however these materials' Гih(inhomogeneous line width)/Гh(homogeneous line width)'s which are the parameters of data multiplicity in PSHB optical memory are an order of unity. For the application of PSHB materials to optical memory, high operating temperature, high Гih/Гh, and rapid reaction rate are wanted. Glass has a superiority on the view point of optical memory application because of its broad inhomogeneous line width and productivity. Our group has discovered room temperature PSHB for Sm2+ in borate glass systems whose Гih/Гh is 24.7 PSHB for rear earth metal in glass matrix has not been studied seriously, yet. It is thought that the study of the relationship between the optical hole and glass structure is necessary.
An overview of recent results concerning molecular doped solids is presented. The hole burning performances and the photophysics of polymer and xerogel-based systems are compared. Three areas are considered in more detail: the problem of electron-phonon coupling, the one of high-temperature persistent spectral hole burning materials, and the search for new frequency-selective photosensitive systems for fast optical pulse processing at 800 nm. This comparison demonstrates that molecular doped polymers and molecular doped xerogels have similar hole burning behavior but mechanisms in these systems can be different. However, in respect of the areas considered, inorganic hosts based on silicate xerogels or porous glasses have shown the best results. Moreover, all the possibilities of hybrid xerogels created by combining inorganic and organic capabilities or by grafting organic species to the host have not yet been revealed.
Persistent spectral hole burning (PSHB) was performed for several porphyrin molecules imbedded in polymer hosts and rare-earth ion Sm2+ doped in BaFCl0.5Br0.5 matrix. Power saturation and broadening effects for hole depth and width were observed. The dynamical process of hole formation was measured and explanation by population rate equations was given. Quantum efficiency of photochemical hole burning was investigated. For BaFCl0.5Br0.5:Sm2+ the capacity of data storage was estimated according to the result of multiple hole burning.