非线性干涉滤光片开关特性及逻辑功能

应用干涉滤光片作为一种光学双稳器件,演示了光学逻辑开关功能。     

InGaAsP/InP有源双稳放大器的实验研究

本文报导了室温下F—P型InGaAsP/InP双异质结半导体激光放大器的双稳态效应,放大器的增益为20dB。     

氩离子激光掺铒光纤的双稳态

分析了掺铒光纤双稳态（ＥＤＦＯＢ）的工作原理、工作条件和特性，并利用氩离子激光（５１４．５ｎｍ）实现了ＥＤＦＯＢ的低功率（＜１０ｍＷ）运转。实验与理论结果基本相符。     

热光双稳态的临界入射功率与临界温升

本文考虑到F—P腔夹层介质和后反射镜均具有一定的吸收时,推导出产生热致色散光学双稳态的临界入射光功率P_c和临界温升△T_c的数学解析表达式。理论计算的 △T_c值与实验值非常符合。为了得到最佳光学双稳态回线和避免腔内的纵向温度梯度,夹层介质和后反射镜应具有一定的匹配吸收。     

Optimization of photo‐aligned ferroelectric liquid‐crystal display under passively addressed driving

Abstract— A ferroelectric liquid‐crystal (FLC) passively addressed 64 × 64 display based on the photo‐alignment technique has been developed. The display matrix has dimensions of 33 × 33 mm², and the FLC layer thickness is about 5 μm. Asymmetric boundary conditions, when only one of ITO surfaces of the display matrix is covered with the photo‐aligning layer while another one is not, have been used for providing both high contrast ratio and steady multiplex operation. The electro‐optical performance of the 5‐μm FLC display is presented, including bistable switching in static operation, optimization in multiplexing operation, and gray‐scale generation.     

Time evolution of entanglement and bistability of two coupled quantum dots in a driven cavity

Abstract

The time evolution of entanglement between two quantum dots (QDs) trapped inside a cavity driven by a coherent quantized field is studied. In the presence of dissipation, entanglement shows many interesting features such as sudden death and revival, and finite steady state value after sudden death. We also investigate dependence of entanglement on dot variables and its relation to bistability. It is found that entanglement vanishes when the cavity field intensity approaches the upper branch of the bistability curve. When the cavity is driven by a modulated field in the presence of dissipation, it can periodically generate entanglement, which is much larger than the maximum value attained in the steady-state for this system but the dots are never fully entangled.     

Optimal homeostasis necessitates bistable control

Bistability is a fundamental phenomenon in nature. In biology, a number of fine properties of bistability have been identified. However, these properties are only consequences of bistability at the physiological level, which do not explain why it had to emerge during evolution. Using optimal homeostasis as the first principle, I find that bistability emerges as an indispensable control mechanism. It is the only solution to a dilemma in glucose homeostasis: high insulin efficiency is required to confer rapidness in plasma glucose clearance, whereas an insulin sparing state is required to guarantee the brain''s safety during fasting. The optimality consideration renders a clear correspondence between the molecular and physiological levels. This new perspective can illuminate studies on the twin epidemics of obesity and diabetes and the corresponding intervening strategies. For example, overnutrition and sedentary lifestyle may represent sudden environmental changes that cause the lose of optimality, which may contribute to the marked rise of obesity and diabetes in our generation. Because this bistability result is independent of the parameters of the mathematical model (for which the result is quite general), some other biological systems may also use bistability to control homeostasis.     

Catalytic constants enable the emergence of bistability in dual phosphorylation

Dual phosphorylation of proteins is a principal component of intracellular signalling. Bistability is considered an important property of such systems and its origin is not yet completely understood. Theoretical studies have established parameter values for multistationarity and bistability for many types of proteins. However, up to now no formal criterion linking multistationarity and bistability to the parameter values characterizing dual phosphorylation has been established. Deciding whether an unclassified protein has the capacity for bistability, therefore requires careful numerical studies. Here, we present two general algebraic conditions in the form of inequalities. The first employs the catalytic constants, and if satisfied guarantees multistationarity (and hence the potential for bistability). The second involves the catalytic and Michaelis constants, and if satisfied guarantees uniqueness of steady states (and hence absence of bistability). Our method also allows for the direct computation of the total concentration values such that multistationarity occurs. Applying our results yields insights into the emergence of bistability in the ERK–MEK–MKP system that previously required a delicate numerical effort. Our algebraic conditions present a practical way to determine the capacity for bistability and hence will be a useful tool for examining the origin of bistability in many models containing dual phosphorylation.     

Origin of rate bistability in Mn–O/Al2O3 catalysts for carbon monoxide oxidation: role of the Jahn–Teller effect

Peculiarities in catalytic activity in carbon monoxide oxidation as well as some structure, electronic and magnetic properties of the three oxide catalysts, Mn³⁺–O/Al₂O₃ (1), Mn³⁺–O–Fe/Al₂O₃ (Mn-substituted spinel, 2) and -Fe₂O₃/Al₂O₃ (3), were studied by kinetic measurements and by Mössbauer spectroscopy. The catalysts 1 and 2 showed a kinetic bistability with a sharp transition towards more reactive state at 200°C (ignition point). In contrast, for catalyst 3, at 200–250°C, the behavior of reaction rate against temperature did not display noticeable hysteresis. On cooling the catalysts 1 and 2, extinction was observed at about 170 and 120°C, respectively, i.e., at 30–80°C lower than the corresponding ignition points. Proximity of activation energy for the high and low activity (15–19 kJ/mol) for both Mn-containing catalysts suggests an increase in the number of active sites at high temperature with no changes in the reaction mechanism. The considerable difference between Mn-containing catalysts 1, 2 and Fe-containing catalyst 3 may be caused by Jahn–Teller (JT) type distortions of the oxygen polyhedron around Mn³⁺. A significant spontaneous axial bond stretching within the local polyhedron seems to diminish Mn–O binding energy, facilitate the participation of surface oxygen species, O_S, in the oxidation of CO by a redox mechanism and promote oxygen vacancies at the surface that would cause considerable effect on the activity. An increase in the width of the counterclockwise hysteresis loop for the catalyst 2 compared to the catalyst 1 indicates that clusters of mixed spinel provide more active sites and more labile O_S species than clusters of the binary Mn oxide.     

Optical Properties of Polymer-dispersed Liquid Crystals

Abstract

Electrooptical properties of polymer-dispersed liquid crystals (LCs) are analyzed from the point of view of the order created by the electric field, dynamic changes of the order (orientation) parameter, and optical transmittivity. Optical phase retardation causes an optical phase shift and is related to thermal effects. Nonlinear optical properties are investigated from the point of view of self-transparency, nonlinear gratings, threshold degenerate wave mixing, optical bistability and second harmonic generation.