“…Hence, it is possible for the quantum efficiency of Tm 3+ to reach 200%. Cross relaxation is closely linked to the distance between ions, [12] and this phenomenon is not obvious at lower concentrations. With increasing doping level, the distance between the ions decreases gradually and, correspondingly, the resonance transmission effect of neighboring Tm 3+ ions occurs more strongly, thereby increasing the luminous intensity of 1.8 µm.…”
Shan-Shan(李珊珊) a) , Xia Hai-Ping(夏海平) a) † , Fu Li(符 立) a) , Dong Yan-Ming(董艳明) a) , Gu Xue-Mei(谷雪梅) a) , Zhang Jian-Li(章践立) a) , Wang Dong-Jie(王冬杰) a) , Zhang Yue-Pin(张约品) a) , Jiang Hao-Chuan(江浩川) b) , and Chen Bao-Jiu(陈宝玖) c) a)
“…Hence, it is possible for the quantum efficiency of Tm 3+ to reach 200%. Cross relaxation is closely linked to the distance between ions, [12] and this phenomenon is not obvious at lower concentrations. With increasing doping level, the distance between the ions decreases gradually and, correspondingly, the resonance transmission effect of neighboring Tm 3+ ions occurs more strongly, thereby increasing the luminous intensity of 1.8 µm.…”
Shan-Shan(李珊珊) a) , Xia Hai-Ping(夏海平) a) † , Fu Li(符 立) a) , Dong Yan-Ming(董艳明) a) , Gu Xue-Mei(谷雪梅) a) , Zhang Jian-Li(章践立) a) , Wang Dong-Jie(王冬杰) a) , Zhang Yue-Pin(张约品) a) , Jiang Hao-Chuan(江浩川) b) , and Chen Bao-Jiu(陈宝玖) c) a)
“…where T g (1) and T g (2) are glass temperature values of the respective homopolymers; W 1 and W 2 are the weight fractions of the two monomers (M 1 , M 2 ); T g (12) is an experimental T g determined from Figure 8 at a polymer composition of 50 mol % that can be evaluated at 75°C; and P 11 , P 22 , P 12 , and P 21 are the monomer distribution probabilities. They are determined as follows 1/P 12 ϭ 1/( ; nЈ ij ϭ (n ij ␣ ij )/⌺ i ⌺ j n ij ␣ ij because each dyad ij has a number of bond rotation ␣ ij and leads to a molar fraction n ij that is weighted to nЈ ij ; ␣ 11 was determined and found to be 22 for the dyad M 1 M 1 .…”
Section: Properties Of the Final Laticesmentioning
confidence: 99%
“…Emulsion polymerization of alkyl (meth)acrylates is well known, and the corresponding latices have found a wide range of industrial applications such as articles, textiles, adhesives, water-based coating, additives, flocculent, and in medical diagnostic tests. 1 One of the most investigated systems is butyl acrylate (BA) that is based on polymer latices. Emulsion copolymerization of BA with some widely used comonomers, for example, styrene (St), vinyl acetate, and other (meth)acrylates such as methyl methacrylate (MMA), was exhaustively investigated with different polymerization processes.…”
“…Theoretical description of the vibrational relaxation leads inevitably to an opensystem dynamics problem (Diestler 1976, Lin 1980, Mukamel 1978. Usually, we pick up an active molecular mode which is taken to be a harmonic oscillator.…”
The primary objective of the present work is an exact theoretical analysis of a vibrational dephasing process. We have investigated a microscopic counterpart of the well known stochastic model of random harmonic oscillator frequency modulation. We have found an exact expression for the oscillator coordinate relaxation. Several principal features of our solution appear to be quite different from the results based on the random frequency modulation model. (i) The envelope function of the oscillator coordinate time dependence is a function of temperature and it reveals definite types of coherent beats. (ii) The 'frequency' of the coordinate oscillations is time dependent and exhibits definite shift relative to the bare oscillator frequency when time goes from zero to infinity. (iii) Both the envelope function and the 'frequency' of the coordinate oscillations depend on the initial oscillator energy. This demonstrates the interaction-introduced non-linearity of the resulting dynamics.
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