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Fuat Bayrakceken, Korkut Yegin, Erdal Korkmaz, Yakup Bakis, Bayram Unal, "Optical Energy Transfer Mechanisms: From Naphthalene to Biacetyl in Liquids and from Pyrazine to Biacetyl", International Journal of Photoenergy, vol. 2012, Article ID 239027, 4 pages, 2012. https://doi.org/10.1155/2012/239027
Optical Energy Transfer Mechanisms: From Naphthalene to Biacetyl in Liquids and from Pyrazine to Biacetyl
Optical energy transfer from naphthalene to biacetyl in liquids at room temperature is studied. Electronically excited naphthalene with 200–260 nm ultraviolet (UV) light emits photons in its emission band and the emitted photons are absorbed by biacetyl, which, in turn, excites biacetyl phosphorescence. The resulting phosphorescence is very stable with emission peak at 545 nm for different excitation wavelengths from 200 to 260 nm. Similar optical energy transfer is also observed from pyrazine to biacetyl. The sensitization of biacetyl by several aromatic donors has been investigated in detail. An aromatic donor, pyrazine, is raised to its first excited singlet state by absorption of ultraviolet radiation. Excitation wavelengths were selected in the first - band of pyrazine. Intersystem crossing in pyrazine is sufficiently fast to give a triplet yield of almost unity as determined by the biacetyl method. The optical excess energy in the biacetyl will be released as light, which is sensitized fluorescence. Biacetyl is the simplest molecule among a wide range of -dicarbonyl compounds, which is important for photophysics and photochemistry applications.
Optical absorption in polar molecules is due to interaction with the permanent dipole moments of individual molecules. The electric field tends to align the dipoles, and the subsequent collision-induced relaxation of the oriented dipoles has a time constant in the picosecond range, giving rise to strong absorption in the far infrared. For nonpolar molecules the much smaller absorption originates in the transient dipole moments induced via collisions in the liquid.
Naphthalene, like many organic compounds, has a conjugated double-bond system, in which every other bond is a double-bond. These conjugated systems have large influence on absorption and emission spectrum of the molecule. Molar absorption coefficient of naphthalene is around 360 and the absorption spectra of naphthalene in rare gas have been extensively studied. The spectra were observed from 333 to 125 nm [1–8]. The transition energies of six transitions were assigned to -electronic states of naphthalene. Symmetry properties of the first two excited singlet states and triplet lifetime were also reported in the context of triplet energy transfer [9–18]. Naphthalene in liquid has a different emission spectra than that of vapor phase, in which room temperature transitions are more defined.
Biacetyl, the compound 2,3-buttanedione, is the simplest molecule among a wide variety of -dicarbonyl compounds, which has been the subject of considerable study for photophysics and photochemistry applications. The ground state of biacetyl is known to be Raman-active and IR-active in not only solid but also liquid and vapor phases. The principle absorption bands are due to - electronic transitions [19, 20]. The absorption and emission spectra of the biacetyl crystal exhibit sharp vibrational structure at low temperatures .
Triplet-triplet energy transfer from naphthalene to biacetyl in vapor phase has been studied in . In that study, decay times for different mixtures of naphthalene and biacetyl were measured under different biacetyl pressures. It was shown that the fluorescence decay time of naphthalene in cyclohexane was 96 ns [23, 24] and 130 ms lifetime for triplet state of naphthalene . In this study, we concentrate on the liquid form of naphthalene and biacetyl at room temperatures as this application of the mixture is quite simple and easy to produce. It is observed that the emission spectrum of biacetyl is very stable. This may open new research directions such that incident light energy can be transferred to different wavelengths as in optical mixers and frequency down-conversion devices.
2. Material and Methods
Biacetyl and naphthalene, were of Aldrich reagent grade, used as received without any further purification, and were mixed at atmospheric pressure. The concentration of biacetyl and naphthalene was between 10−3 and 10−4 M, with the relative concentration of naphthalene/biacetyl 1⁄2 to 1⁄3 for best emission. Two Princeton Instruments Acton Advanced SP2300 model monochromators were used for all optical measurements. These devices have 600 g/mm grating with a focal length of 300 mm. The measurement setup is illustrated in Figure 1. A 500 W Xenon bulb was placed in front of the entrance slit of monochromator-1 to obtain maximum amplitude, and the entrance and exit slits were adjusted to 650 μm openings. A computer-controlled software adjusts monochromatic beams with 200–300 nm wavelength with a 10 nm step and they were emitted from the exit of monochromator-1. A quartz lens was used to focus emitted beam on the sample. The excited sample emitted beam perpendicular to the excitation beam. This emitted beam was focused on the slit of monochromator-2 with the sequential lenses. The alignment was carried out using microstage to obtain the maximum amplitude from the excited beam. The excited beam was scattered from the quartz tube and liquid interface, however the luminescence was due to the entire mixture. Since the focusing was oriented to the center of the liquid mixture, where the luminescence was dense, the excited beam did not reach and interfere with the monochromator-2. Computer-controlled scan has been performed at monochromator-2 between 300–750 nm with a step of 1 nm and 500 ms period. The emitted beam entering through the 650 μm slit from monochromator-2 was converted to electrical signals by means of the photomultiplier tube (PMT) depending on the emission amplitude. These signals were further recorded digitally in a computer through a data scan software. Dark room was used for all measurements and measurements were performed at room temperature. The emitted beam reaching the PMT was posed with 500 ms period. Because the Xenon bulb was wavelength filtered at 200–260 nm and the PMT was sensitive to the wavelength, a normalization had to be carried out. For that reason, the sample was replaced with a quartz mirror in the measurement setup and the measurement was repeated. The peaks of excitations have been obtained. The maximum amplitude obtained at 220 nm was used to calculate the normalization coefficient for each excitation wavelength. These coefficients, then were multiplied with the entire spectrum to perform the required normalization.
The setup displayed in Figure 1 was also used to study optical energy transfer from pyrazine to biacetyl. Biacetyl and pyrazine, were of Aldrich reagent grade, used as received without any further purification and were mixed at atmospheric pressure. The concentration of biacetyl and pyrazine was between 10−3 and 10−4 M, with the relative concentration of pyrazine/biacetyl 1⁄2 for the best emission.
3. Results and Discussion
The sensitization of biacetyl fluorescence by naphthalene has been investigated in detail. The emission spectrum of naphthalene-biacetyl is shown in Figure 2, where the mixture is excited from 220 to 260 nm monochromatic source. Peak emission at 545 nm is common to all excitation wavelengths. Side peaks at 491 nm and 610 nm were also observed with relative amplitudes of 0.51 and 0.47 of peak quantum efficiency, respectively. The emission spectrum of the mixture is very stable and common to all excitation wavelengths. Thus, it makes this solution an ideal candidate for photomixing applications.
An aromatic donor is excited to its first excited singlet by absorbing ultraviolet radiation. In addition, the triplet state of the donor molecules are also populated. If an acceptor molecule (i.e., biacetyl) is present, the donor (i.e., naphthalene) can transfer the electronic energy to the acceptor, in which, in turn, the acceptor molecule raises to its lowest triplet state. Excited biacetyl molecules will emit phosphorescence which will be termed as sensitized phosphorescence because the acceptor molecules do not initially absorb incident light. In this study, the donor molecule is naphthalene in liquid and the acceptor molecule is biacetyl in liquid. Hence, the phosphorescence emission of naphthalene will be absorbed by acceptor molecule biacetyl in its triplet state, then excess energy will be emitted as light at different frequencies.
For 200 to 260 nm laser light is absorbed by naphthalene, but at 545 nm, neither naphthalene nor biacetyl absorb light; hence, the system is totally transparent for 545 nm emission line. The optical pumping at 200 to 260 nm excites naphthalene molecules to their first excited singlet level, then excited naphthalene molecules decay back to ground state by fluorescence emission of naphthalene where this emission band of naphthalene coincides with the excitation band of biacetyl. Therefore, the biacetyl molecules will be electronically excited by naphthalene. Excited biacetyl molecules will return to their ground state by fluorescence and phosphorescence emissions. This process is depicted in the following scheme which is summarizing naphthalene and biacetyl interaction: (1) Naph + BiA + hv (200–260 nm light) → Naph* + BiA Naphthalene (Naph) absorbs 200–260 nm light, but BiA does not absorb this light, hence only Naph is electronically excited and BiA is still in the ground state;(2) Naph* + BiA → Naph + hv (emitted from Naph) + BiA;(3) Naph + hv (emitted from Naph) + BiA → Naph + BiA*; BiA* is electronically excited by absorbing the emission of Naph;(4) Naph + BiA* → Naph + BiA + hv (400–650 nm emitted from BiA).
The sensitization of biacetyl fluorescence by pyrazine has been investigated in detail, in an attempt to be validated by biacetyl method. Emission spectrum of pyrazine-biacetyl is shown in Figure 3 where the mixture is excited from 305 to 325 nm monochromatic source. Peak emission at 460 nm is common to all excitation wavelengths.
A brief description of the biacetyl methods is as follows. An aromatic donor will be raised to its first excited singlet by absorption of ultraviolet radiation. Among other processes, which will subsequently occur, the triplet state of the donor molecules will also be populated. If a suitable acceptor molecule (i.e., biacetyl) is present, the electronic energy of the donor, pyrazine, can be transferred to the biacetyl producing a biacetyl molecule in its first singlet state. Excited singlet biacetyl molecules so produced will emit fluorescence lights as well as phosphorescence lights. This behavior is labeled as sensitized fluorescence and sensitized phosphorescence, since emissions occur without the emitting molecule initially absorbing light energy. Comparing the quantum yield of the sensitized fluorescence with that produced in a separate experiment, where biacetyl itself is excited affords as determination of the triplet yield of aromatic donor. The triplet yield is, in essence, a measure of the number of singlet donor molecules, which eventually cross over into the triplet manifold. The following reaction mechanism is typical for optical energy transfer from donor to acceptor molecules. Pyrazine emits light as fluorescence and this light will be absorbed by the acceptor molecule biacetyl, then this optical excess energy in the biacetyl will be released as light, which is sensitized fluorescence. This process is shown in the following scheme which is summarizing pyrazine and biacetyl interaction: (1) Pyz + BiA + hv (305–325 nm light) → Pyz* + BiA Pyz absorbs 305–325 nm light, but BiA does not absorb this light, hence only Pyz iselectronically excited and BiA is still in the ground state;(2) Pyz* + BiA → Pyz + hv (emitted from Pyz) + BiA;(3) Pyz + hv (emitted from Pyz) + BiA → Pyz + BiA*; BiA* is electronically excited by absorbing the emission of Pyz;(4) Pyz + BiA* → Pyz + BiA + hv (450–600 nm emitted from BiA).
We show that donor molecule pyrazine emits light and biacetyl absorbs this light as an optical receiver. Similar mechanism is also observed for naphthalene and biacetyl, where donor molecule naphthalene emits light and biacetyl absorbs this light as an optical receiver. Therefore, this mechanism is called an optical antenna at the nanosecond time domain. In our study, neither excimer nor exciplex fluorescence could be recorded.
- D. W. Turner, C. Baker, and C. R. Brundle, Molecular Photoelectron Spectroscopy, John Wiley & Sons, 1970.
- C. A. Parker, Photoluminescence of Solutions, Elsevier, Amsterdam, The Netherlands, 1968.
- J. B. Birks, Photophysics of Aromatic Molecules, Wiley-Interscience, London, UK, 1970.
- F. Bayrakceken, “Radiative electronic energy transfer-time studies of naphthalene-biacetyl system by one and two-photon excitation, and optical antenna mechanism,” Spectrochimica Acta Part A, vol. 61, no. 6, pp. 1069–1074, 2005.
- C. A. Parker and C. G. Hatchard, “Sensitised anti-stokes delayed fluorescence,” Proceedings of the Chemical Society, pp. 386–387, 1962.
- C. A. Parker and T. A. Joyce, “Phosphorescence of benzophenone in fluid solution,” Chemical Communications, no. 13, pp. 749–750, 1968.
- J. H. D. Eland and C. J. Danby, “Inner ionization potentials of aromatic compounds,” Zeitschrift Für Naturforschung 239, p. 355, 1968.
- E. Koch, A. Otto, and K. Radler, “The vacuum ultraviolet spectrum of naphthalene vapour for photon energies from 5 to 30 eV,” Chemical Physics Letters, vol. 16, no. 1, pp. 131–135, 1972.
- H. W. Offen and D. T. Phillips, “Fluorescence lifetimes of aromatic hydrocarbons under pressure,” The Journal of Chemical Physics, vol. 49, no. 9, pp. 3995–3997, 1968.
- J. B. Birks, Organic Molecular Photophysics, vol. 1-2, John Wiley & Sons, 1973.
- U. Laor and P. K. Ludwig, “Excitation from 3080–2150 Å,” The Journal of Chemical Physics, vol. 54, no. 3, pp. 1054–1057, 1971.
- T. N. Singh-Rachford, A. Haefele, R. Ziessel, and F. N. Castellano, “Boron dipyrromethene chromophores: next generation triplet acceptors/annihilators for low power upconversion schemes,” Journal of the American Chemical Society, vol. 130, no. 48, pp. 16164–16165, 2008.
- E. B. Priestly and A. Haug, “Phosphorescence spectrum of pure crystalline naphthalene,” Journal of Chemical Physics, vol. 49, no. 2, p. 622, 1968.
- T. N. Singh-Rachford and F. N. Castellano, “Supra-nanosecond dynamics of a red-to-blue photon upconversion system,” Inorganic Chemistry, vol. 48, no. 6, pp. 2541–2548, 2009.
- P. E. Keivanidis, S. Baluschev, T. Miteva et al., “Up-conversion photoluminescence in polyfluorene doped with metal(II)-octaethyl porphyrins,” Advanced Materials, vol. 15, no. 24, pp. 2095–2098, 2003.
- R. R. Islangulov, D. V. Kozlov, and F. N. Castellano, “Low power upconversion using MLCT sensitizers,” Chemical Communications, no. 30, pp. 3776–3778, 2005.
- S. Baluschev, J. Jacob, Y. S. Avlasevich et al., “Enhanced operational stability of the up-conversion fluorescence in films of palladium-porphyrin end-capped poly(pentaphenylene),” ChemPhysChem, vol. 6, no. 7, pp. 1250–1253, 2005.
- S. Baluschev, V. Yakutkin, G. Wegner et al., “Two pathways for photon upconversion in model organic compound systems,” Journal of Applied Physics, vol. 101, no. 2, Article ID 023101, 2007.
- J. C. D. Brand and A. W.-H. Mau, “Low-lying electronic states of biacetyl,” Journal of the American Chemical Society, vol. 96, no. 14, pp. 4380–4385, 1974.
- J. M. Leclercq, C. Mijoule, and P. Yvan, “Theoretical investigations of excited states of glyoxal and biacetyl,” The Journal of Chemical Physics, vol. 64, no. 4, pp. 1464–1472, 1976.
- J. W. Sidman and D. S. McClure, “Electronic and vibrational states of biacetyl and biacetyl-d6,” Journal of the American Chemical Society, vol. 77, no. 24, pp. 6461–6474, 1955.
- F. Bayrakçeken, O. J. Demir, L. Tunçyürek, and I. S. Karaaslan, “Triplet-triplet energy transfer from naphthalene to biacetyl in the vapor phase,” Spectrochimica Acta Part A, vol. 65, no. 1, pp. 27–31, 2006.
- O. Demir, B. DiBartolo, and F. Bayrakceken, Bulletin of the American Physical Society, vol. 26, no. 6, p. 796, 1981.
- Y. Chen, L. Pei, J. Jin, Y. Gao, X. Ma, and C. Chen, “Laser-induced fluorescence spectroscopy of biacetyl A1(S1)–X1(S0)),” Chemical Physics Letters, vol. 323, no. 1-2, pp. 125–129, 2000.
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