1000 resultados para ER3 PHOSPHOR FILMS


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The upconversion emission of Er<sup>3+</sup>/Yb<sup>3+</sup> codoped phosphate glass with 980 nm excitation was investigated. In the glass Er<sup>3+</sup> concentration has a great influence on the intensity and the ratio of green and red light upconversion. The slope of the green luminenscence intensity as a function of pumping power ranges from 2.52 to 3.27, is the evidence of the three photon excitation process. The three photon process can also be concluded from excitation spectra when emission wavelength is 545 nm. The effect of Er<sup>3+</sup> concentration is also discussed.

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2.0 &mu;m spectroscopic properties of Er<sup>3+</sup>/Tm<sup>3+</sup>/Ho<sup>3+</sup> triply-doped fluorophosphate glasses pumped by 808 nm and the energy transfer mechanisms between the three rare earth ions were investigated. J-O theory was used to calculate the parameters of Ho<sup>3+</sup> in fluorophosphate glasses. Absorption and emission cross-sections and the gain coefficients were calculated. The obtained lifetime r and spontaneous transition probability Ar of Ho<sup>3+</sup>:<sup>5</sup>I<inf>7</inf> level were 10.64 ms and 93.95 s<sup>-1</sup> respectively. The calculated maximum emission cross-section of 2.0 &mu;m was 9.26&times;10<sup>-21</sup> cm<sup>2</sup>. The energy transfer analysis indicated that the cross-relaxation of Tm<sup>3+</sup> was important and the resonent energy transfer in Er<sup>3+</sup>&rarrHo<sup>3+</sup>, Tm<sup>3+</sup>&rarrHo<sup>3+</sup>, Er<sup>3+</sup>&rarrTm<sup>3+</sup>&rarrHo<sup>3+</sup> process was the main channel. The study revealed that the Er<sup>3+</sup>/Tm<sup>3+</sup>/Ho<sup>3+</sup> triply-doped fluorophosphate glass would be a potential material for 2.0 &mu;m emission because of the efficient sensitization of Er<sup>3+</sup> and Tm<sup>3+</sup> to Ho<sup>3+</sup>.

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To study the effects of upconversion in Erbium, a set of rate equations that simulates the performance of the passively Q-switched Er:Yb:glass laser with a Co<sup>2+</sup>:MgAl<inf>2</inf>O<inf>4</inf> saturable absorber was set up. The dynamics of the Er<sup>3+</sup> excited state and the effect of upconversion on the passively Q-switched laser are obtained through numerical simulation of the model. It is found that the impact ratios of upconversion effect on the peak power of the passively Q-switched laser pluse and the repetition rate are both decreased with the increase of pump power.

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Er3+-doped halide modified tellurite glasses were synthesized by conventional melting and quenching method. The Judd-Ofelt analysis was performed on the absorption spectra and the transition probabilities, excited state lifetimes, and the branching ratios were calculated and discussed. The intense infrared and visible fluorescence spectra under 980 nm excitation were obtained. Strong upconversion signal was observed at pumping power as low as 30 mW in the glasses with halide ions. The upconversion mechanisms and power dependent intensities were discussed, which showed two-photon process are involved for the green and red emissions. The decay times of the emitting states and the corresponding quantum efficiency were determined and explained. (C) 2004 American Institute of Physics.

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Infrared-to-visible upconversion fluorescence of Er(3+)/Yb(3+) co-doped lithium-strontium-lead-bismuth (LSPB) glasses for developing potential upconversion lasers has been studied under 975-nm excitation. Based on the results of energy transfer efficiency and upconversion spectra, the optimal Yb(3+)-Er(3+) concentration ratio is found to be 5:1. Intense green and red emissions centered at 525, 546, and 657 nm, corresponding to the transitions 2H_(11/2)--&gt4I_(15/2), 4S_(3/2)--&gt4I_(15/2), and 4F_(9/2)--&gt4I_(15/2), respectively, were observed. The quadratic dependence of the 525-, 546-, and 657-nm emissions on excitation power indicates that a two-photon absorption process occurs under 975-nm excitation. The high-populated 4I_(11/2) level is supposed to serve as the intermediate state responsible for the upconversion processes. The intense upconversion luminescence of Er(3+)/Yb(3+) co-doped LSPB glasses may be a potentially useful material for developing upconversion optical devices.

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For the first time. effect of halide ions (F-, Cl-, Br-, and I-) introduction on structure, thermal stability, and upconversion fluorescence in Er3+/Yb3+-codoped oxide-halide germanium-bismuth glasses has been systematically investigated. The results show that halide ions modified germanium-bismuth glasses have lower maximum phonon energy and phonon density, worse thermal stability. longer measured lifetimes of I-4(l1/2) level, and stronger upconversion emission than germanium-bismuth glass. All these results indicate that halide ions play an important role in the formation of glass network, and have an important influence on the upconversion luminescence. The possible upconversion mechanisms of Er3+ ion are also evaluated. &COPY; 2005 Elsevier Ltd. All rights reserved.

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We report on the energy transfer and frequency upconversion spectroscopic properties of Er3+-doped and Er3+/Yb3+-codoped TeO2-ZnO-Na2O-PbCl2 halide modified tellurite glasses upon excitation with 808 and 978 nm laser diode. Three intense emissions centered at around 529, 546 and 657 nm, alongwith a very weak blue emission at 4 10 nm have clearly been observed for the Er3+/Yb3+-codoped halide modified tellurite glasses upon excitation at 978 nm and the involved mechanisms are explained. The quadratic dependence of fluorescence on excitation laser power confirms the fact that the two-photon contribute to the infrared to green-red upconversion emissions. And the blue upconversion at 410 nm involved a sequential three-photon absorption process. (c) 2005 Elsevier Ltd. All rights reserved.

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The Raman spectra, infrared spectra and upconversion luminescence spectra were studied, and the effect mechanism of OH- groups on the upconversion luminescence of Er3+-doped oxyhalide tellurite glasses was analyzed. The results show that the phonon energy of lead chloride tellurite (PCT) glass was lower than that of lead fluoride tellurite (PFT) glass, but upconversion luminescence intensity of Er3+-doped PFT glass was higher than that of Er3+-doped PCT glass. The analysis considers that it was attributed mainly to the effect of OH- groups. The lower the absorption coefficient of the OH- groups, the higher the fluorescence lifetime of Er3+, and as a result the higher upconversion luminescence intensity of Er3+. In this work, the effect of OH groups on the upconversion luminescence of Er3+ was bigger than that of the phonon energy. (c) 2005 Elsevier Inc. All rights reserved.

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Blue, green and red emissions through frequency upconversion and energy transfer processes in Tm3+/Er3+/Yb3+-codoped oxyhalide tellurite glass under 980 nm excitation are investigated. The intense blue (476 nm), green (530 and 545 nm) and red (656 nm) emissions are simultaneously observed at room temperature. The blue (476 nm) emission was originated from the (1)G(4)->H-3(6) transition of Tm3+. The green (530 and 545 nm), and red (656 nm) upconversion luminescences were identified from the H-2(11/2)->I-4(15/2), S-4(3/2)->I-4(15/2), and F-4(9/2)->I-4(15/2) transitions of Er3+, respectively. The energy transfer processes and possible upconversion mechanisms are evaluated. (C) 2005 Elsevier B.V. All rights reserved.

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The upconversion properties of Er3+-doped heavy metal oxyfluoride germanate glasses under 975 nm excitation have been investigated. The intense green (551 and 529 nm) and relatively weak red (657 nm) emissions corresponding to the transitions S-4(3/2) -> I-4(15/2), H-2(11/2) -> I-4(15/2) and F-4(9/2) -> I-4(15/2), respectively, were simultaneously observed at room temperature. The content of PbF2 has an important influence on the upconversion luminescence emission. With increasing content of PbF2, the intensities of green (529 nm) and red (657 nm) emissions increase slightly, while the green emission (551 nm) increases markedly. These results suggest that PbF2 has an influence on the green (551 nm) emission more than on the green (529 nm) and red (657 nm) emissions.