FLUORESCENCE, DEFECT FLUORESCENCE, AND PHOSPHORESCENCE SPECTRA AT 4.2 °K OF UNDOPED AND β-METHYLNAPHTHALENE-DOPED NAPHTHALENE CRYSTALS

1966 ◽  
Vol 44 (7) ◽  
pp. 1485-1515 ◽  
Author(s):  
F. R. Lipsett ◽  
G. Macpherson

Fluorescence, defect fluorescence, and phosphorescence spectra were obtained at 4.2 °K from undoped crystals containing unwanted impurities and from crystals deliberately doped with β-methylnaphthalene. The doped crystals included normal and fully deuterated naphthalene and β-methylnaphthalene in all combinations. Fluorescence attributable to physical defects, analogous to that recently reported for anthracene, was found in all crystals. This fluorescence consisted of bands rather than lines, and occurred in the spectral region between fluorescence (singlet emission) and phosphorescence (triplet emission). The excitation spectrum (intensity of the fluorescence as a function of excitation wavelength) showed one of two forms depending on the fluorescence band chosen, which indicated that the defect fluorescence may be excited either directly or by energy transfer, similarly to other modes of luminescence. The decay time of the defect fluorescence was < 0.01 second, indicating that the defect states are probably disturbed naphthalene singlet states.Moderately intense phosphorescence consisting of lines was found in all of the doped crystals. Assignments of the lines could not be made because of the large number of lines present. However, probable values of the triplet 0–0 levels of normal and deuterated naphthalene and β-methylnaphthalene were deduced from the present and related experiments. The undoped crystals showed a few very weak phosphorescence lines superimposed on a weak continuum of fluorescence. Those crystals with the fewest lines were the purest, and showed a decay time of line plus continuum < 0.01 second, confirming that pure naphthalene is not phosphorescent at 4.2 °K. Phosphorescence excitation spectra, decay times, and temperature dependences were found. For the doped crystals, the decay times ranged from < 0.01 to 18 seconds and the phosphorescence intensity at 10–12 °K fell to half the value at 4.2 °K, indicating an activation energy of about 37 cm−1. The phosphorescence excitation spectrum, decay time, and temperature dependence of naphthalene-d8 doped with β-methylnaphthalene were dissimilar to those of the other doped crystals, for reasons which are not yet understood.The fluorescence spectra consisted of lines for both undoped and doped crystals. The results were tabulated and compared with those of other research workers. It was not possible, however, to assign each line, to either a particular material or a particular vibrational mode.

1972 ◽  
Vol 27 (5) ◽  
pp. 756-759 ◽  
Author(s):  
H. Dreeskamp ◽  
O. Hutzinger ◽  
M. Zander

Abstract Absorption spectra in liquid solution, fluorescence and phosphorescence spectra, phosphores-cence quantum yields, phosphorescence to fluorescence quantum yield ratios, and phosphorescence decay times of 9 chloro substituted biphenyls dissolved in low temperature EPA glass were in-vestigated. The emission spectra of sterically unhindered systems are structured and significantly Stokes-shifted. Ortho substitution shifts the conjugation band in absorption as well as the un-structured fluorescence and phosphorescence bands to shorter wave lengths presumably by pre-venting the system from attaining a planar excited state. Chloro substitution which increases the rate constant of phosphorescence in the order meta < para < ortho, is nearly additive for multiple substituted systems and is correlated to the MO coefficients at the chloro substituted position in the absence of steric hindrance


1988 ◽  
Vol 42 (5) ◽  
pp. 891-896 ◽  
Author(s):  
Charles F. Pace ◽  
Steven M. Thornberg ◽  
Jon R. Maple

An inexpensive, simple (but highly automated) instrument for acquiring high-resolution fluorescence and phosphorescence spectra of polycyclic aromatic hydrocarbons (PAHs) is described. Fluorescence and phosphorescence signals are processed by gated integration and photon counting, respectively. The instrument can be used to acquire excitation as well as emission spectra in both the frequency and time domain. In addition, a method for measuring single and double exponential phosphorescence decay times is presented. Decay times ranging from 0.3 ms to 300 ms were measured for several naphthalene derivatives, with a precision of ∼10%. The primary advantages of this instrument are high sensitivity, high selectivity, wide linear dynamic ranges, and a versatile range of applications.


1976 ◽  
Vol 31 (8) ◽  
pp. 987-989 ◽  
Author(s):  
F. Fratev ◽  
O.E. Polansky ◽  
M. Zander

AbstractFrom the fluorescence and phosphorescence spectra of several aromatic amines it is concluded that the conjugation between nitrogen and aryl groups in the excited state is restricted. With this result a sterical explanation for the lack of the expected photochemical carbazole ring closure of 1-and 2-anilino naphthalene is given.


2011 ◽  
Vol 04 (03) ◽  
pp. 289-293 ◽  
Author(s):  
WEI ZENG ◽  
YUHUA WANG ◽  
XUHUI XU ◽  
YU GONG

A new green emitting long-lasting phosphor Ca2ZnSi2O7:Eu2+ has been synthesized through the high temperature solid-state method. The excitation spectrum of [Formula: see text] shows a broadband attributed to 8S7/2–4f65d1 transition of Eu2+ ions. Both of the fluorescence and phosphorescence spectra showed a broadband centered at 528 nm, corresponding the only one Ca2+ site in Ca2ZnSi2O7 . The relationship of emission wavelength and Eu–O distance is investigated. Its afterglow can be seen with the naked eye in the dark clearly for 2 h after removal of the excitation source. Oxygen vacancy [Formula: see text] and zinc vacancy [Formula: see text], two different kinds of traps are proposed and their contrary influence on afterglow is discussed.


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