Modelling of switching in surface-stabilized ferroelectric liquid crystal cells using a three-variable model in one dimension

The switching process in ferroelectric liquid crystal devices takes place through the formation and evolution of domains, which is modelled here using a three-variable approach. This approach includes variation of the director profile in one dimension, through the thickness of the cell. Here we discuss details of the model which are necessary in order to reproduce the domain nucleation and switching times as a function of applied voltage for both monopolar and bipolar pulses. We show that the three-variable modelling of SSFLC switching in one dimension produces excellent comparisons with experimental data for both bipolar and monopolar pulses.     

Modelling monopolar and bipolar switching in ferroelectric liquid crystal devices using a three variable theory

The switching process in ferroelectric liquid crystal devices takes place through the formation and evolution of domains, which can be modelled using a three variable approach. Here we discuss details of the model which are necessary in order to reproduce the domain nucleation and switching times as a function of applied voltage for both monopolar and bipolar pulses. We show that in order to reproduce data correctly the model must incorporate a complex empirical elastic stress term.     

Optical studies of dynamic director configurations in ferroelectric liquid crystal devices

An investigation into the transmission spectrum of a ferroelectric liquid crystal device is undertaken. This is done both for an initial static state and during a switching process. Comparisons are made between experimental data and theoretical predictions. The dynamic internal director configurations in the device is shown to be consistent with a simple model during both monopolar and bipolar addressing pulses.     

Optical studies of dynamic director configurations in ferroelectric liquid crystal devices

An investigation into the transmission spectrum of a ferroelectric liquid crystal device is undertaken. This is done both for an initial static state and during a switching process. Comparisons are made between experimental data and theoretical predictions. The dynamic internal director configurations in the device is shown to be consistent with a simple model during both monopolar and bipolar addressing pulses.     

Modelling of addressing schemes in surface stabilized ferroelectric liquid crystal cells using a three variable model in one dimension

The 'Three-Variable Model in One Dimension' has been successfully used to model the domain switching process for simple monopolar and bipolar pulses. In this paper, we discuss the development of this model to describe the switching process due to more complicated addressing waveforms. We have taken two contrasting addressing schemes: the Seiko scheme which is a simple example of a low voltage addressing scheme, and the Joers Alvey scheme, a high voltage addressing scheme which utilizes the high biaxiality properties of a ferroelectric liquid crystal (FLC) material. We experimentally simulate the voltage sequence 'seen' by a pixel subject to these addressing schemes, and take into consideration the worst case combinations of voltages that could cause switching and non-switching conditions. We show that the 'Three Variable Model in One Dimension' is in excellent agreement with experimental data for the Seiko addressing scheme, and can be used to predict the operating regime for the Joers Alvey addressing scheme.     

The dissociation rate of water molecules in systems with cation- and anion-exchange membranes

Within the framework of the mathematical model of Nernst-Planck-Poisson, an attempt is undertaken to theoretically describe the electrodiffusion of ions in the system diffusion layer/monopolar ionexchange membrane, which is accompanied by dissociation of water molecules. The formulas for estimating the current density transferred through a monopolar membrane by hydrogen or hydroxyl ions formed in dissociation of water in the space-charge region are derived. The rate constants and other parameters of dissociation of water molecules in the space-charge region of monopolar membranes under conditions of stabilization of the diffusion layer thickness are calculated. Their comparative analysis with the similar characteristics of bipolar membranes is carried out. For the phosphoric-acid heterogeneous membrane MK-41 in which the polarization conditions in the current density range under study are not so severe and the reaction layer is not being depleted as in the bipolar membrane MB-3 (contains the same phosphoric-acid groups), it is shown that only single-charged phosphoric-acid groups are involved in the water dissociation reaction. For MK-41, the calculated constants of the heterolytic reaction of water molecule dissociation are lower than for the heterogeneous membrane MA-40 containing ternary and quaternary amino groups. It is confirmed that the nature of ionogenic groups in membranes is a factor that determines the rate of water dissociation in systems with ion-exchange membranes.     

Membrane Potential of Composite Bipolar Membrane in Ethanol-Water Solutions: The Role of the Membrane Interface

The membrane potential across a composite bipolar membrane (CBM) composed of a cation-exchange membrane with an anion-exchange membrane is theoretically and experimentally analyzed for LiCl ethanol-water solutions. The theoretical approach is based on an extension of the Donnan equilibrium and the Nernst-Planck equation of monopolar charged membranes for the case of two ion-exchange layers by considering the effect of electrolyte ion pairing in the external solution. The experimental results show that the effective membrane charge densities of the two ion-exchange layers will become smaller than those which are separately estimated for each layer. We have introduced a contact factor, zeta, into the theoretical approach to clarify this phenomenon in this study, and the theoretical predictions were in good agreement with the experimental data. The membrane potential measurements show that CBM has the characteristics of a bipolar membrane and can significantly contribute to a better electrochemical characterization of the CBMs. Copyright 1999 Academic Press.     

Dual defects of cation and anion in memristive nonvolatile memory of metal oxides

The electrically driven resistance change of metal oxides, called bipolar memristive switching, is a fascinating phenomenon in the development of next-generation nonvolatile memory alternatives to flash technology. However, our understanding of the nature of bipolar memristive switching is unfortunately far from comprehensive, especially the relationship between the electrical transport and the local nonstoichiometry. Here we demonstrate that the coexistence of anion and cation defects is critical to the transport properties of NiO, one of the most promising memristive oxides, by utilizing first-principles calculations. We find that, in the presence of both nickel and oxygen defects, which must exist in any real experimental systems, carrier concentrations of holes generated by nickel defects can be modulated by the presence or absence of oxygen defects around the nickel defect. Such alternation of local nonstoichiometry can be understood in terms of an oxygen ion drift induced by an external electric field. This implication provides a foundation for understanding universally the nature of bipolar memristive switching in various p-type metal oxides.     

Cell membrane electropermeabilization by symmetrical bipolar rectangular pulses. Part I. Increased efficiency of permeabilization

The paper presents a comparative study of electropermeabilization of cells in suspension by unipolar and symmetrical bipolar rectangular electric pulses. While the parameters of electropermeabilization by unipolar pulses have been investigated extensively both in cell suspensions and in tissues, studies using bipolar pulses have been rare, partly due to the lack of commercially available bipolar pulse generators with pulse parameters suitable for electropermeabilization. We have developed a high-frequency amplifier and coupled it to a function generator to deliver high-voltage pulses of programmable shapes. With symmetrical bipolar pulses, the pulse amplitude required for the permeabilization of 50% of the cells was found to be approximately 20% lower than with unipolar pulses, while no statistically significant difference was detected between the pulse amplitudes causing the death of 50% of the cells. Bipolar pulses also led to more than 20% increase in the uptake of lucifer yellow. We show that these results have a theoretical background, because bipolar pulses (i) counterbalance the asymmetry of the permeabilized areas at the poles of the cell which is introduced by the resting transmembrane voltage, and (ii) increase the odds of permeabilization of cells having a nonspherical shape or a nonhomogeneous membrane. If similar results are also obtained in tissues, bipolar pulse generators could in due course gain a wide, or even a predominant use in cell membrane electropermeabilization.     

The low frequency conductance of bipolar membranes demonstrates the presence of a depletion layer

The electrical conductance of a 2-sheet bipolar membrane was measured as a function of frequency over the range 0.1 Hz–10 kHz in electrolyte solutions containing 1, 10 and 100 mM KCl. The 2-sheet bipolar membrane was also separated into its monopolar regions and their electrical properties were examined individually. The low frequency conductance of the bipolar membrane was always significantly less than the value which would have been obtained if the monopolar regions were too far apart to interact. The data suggest that the separation of the ion exchange regions was approximately ≤1 nm, even in the absence of a large DC current.     

Dielectric relaxation on the intermediate layer in a bipolar membrane under the water splitting phenomenon. I. Shift of the dielectric properties by means of time-dependent impedance measurements

In this study, we examined the dielectric properties of an intermediate layer in a bipolar membrane, which is composed of a negatively charged layer and a positively charged layer joined in series. As a result of the time-dependent impedance measurements of charged membranes, the negative increment in electric conductivity and the positive increment in electric capacity were observed only in the case of a bipolar membrane under the application of reverse-biased voltages, which were quite different from the behavior of both monopolar membranes and of a bipolar membrane under forward-biased voltages. Further, the observed shifts showed a nearly constant value against the reverse-biased voltage. It is concluded that these characteristics coincide with the process of ion exclusion in the intermediate layer and are attributed to the water splitting mechanism.     

Bistable electro-optical switching in the smectic I* phase of a ferroelectric liquid crystal

The ferroelectric switching behaviour of the highly ordered smectic I* phase has been investigated in the mixture which shows a S*_I phase at room temperature. The bistability was obtained in a 3.5μm thick cell. Director switching and the reorientation processes have been studied by applying symmetric square and triangular wave pulses. It has been found that an asymmetric switching occurs in the smectic I* phase for low electric fields due to the hexagonal ordering of the molecules in the layer. This asymmetric switching was confirmed by optical microscopy and four stable states have been observed for low electric field. For higher electric fields only one state is stabilized which results in symmetric switching by both methods in the smectic I* phase.     

Correction of pH of diluted solutions of electrolytes by electrodialysis with bipolar membranes

The current efficiencies of the water dissociation water and the voltage-current characteristics of the bipolar (asymmetric bipolar) membranes were measured in a two-chamber electrochemical cell. The cell was formed of an MB-3 bipolar membrane or an asymmetric bipolar membrane, which is an MA-40 heterogeneous membrane with a thin surface layer in the form of a cation-selective homogeneous film and MA-40 and MA-41 heterogeneous monopolar membranes. The dissociation of water on MA-40 in 0.01 M sodium chloride decreased the current efficiency of the acid and alkali both in the channel with a bipolar membrane and in the channel with an asymmetric bipolar membrane. The effective ion transport numbers across MA-40 and MA-41 at different pH values were determined. The water dissociation rate on MA-40 decreased at pH > 9.5. A kinetic model of the electrodialysis of a dilute solution of sodium chloride in a two-chamber unit cell with a bipolar and anionite membranes was suggested.     

Electromagnetically induced transparency with quantum interferometry

We have shown that electromagnetically induced transparency can be achieved by control-probe interferometry using two delayed phase-locked ultrashort pulses. Two vibrational wavepackets on the excited state, excited by two delayed phase-locked ultrashort pulses, interfere constructively or destructively leading to enhancement or suppression of absorption to a selective set of vibrational levels. Depending on the phase difference and the delay between the pulses with same carrier frequency, one can design different transparency windows between absorption peaks at consecutive even(odd) vibrational levels by eliminating absorption at odd(even) vibrational levels. We have shown that by switching the phase difference of two delayed femtosecond pulses, one can switch to complete elimination of absorption from enhanced absorption to a particular set of vibrational levels in the excited state. Thus, switching of transparency through window between odd vibrational levels to that between even vibrational levels is possible. By properly choosing the temporal width and the carrier frequency of the pulses, lossless transmission of complete or bands of frequencies of the pulses can be achieved through these transparency windows. Hence, designing of single- or multi-mode transparency windows in NaH molecule is feasible by control-probe quantum interferometry.     

3D electrogenerated chemiluminescence: from surface-confined reactions to bulk emission

Among luminescence techniques, electrogenerated chemiluminescence (ECL) provides a unique level of manipulation of the luminescent process by controlling the electrochemical trigger. Despite its attractiveness, ECL is by essence a 2D process where light emission is strictly confined to the electrode surface. To overcome this intrinsic limitation, we added a new spatial dimension to the ECL process by generating 3D ECL at the level of millions of micro-emitters dispersed in solution. Each single object is addressed remotely by bipolar electrochemistry and they generate collectively the luminescence in the bulk. Therefore, the entire volume of the solution produces light. To illustrate the generality of this concept, we extended it to a suspension of multi-walled carbon nanotubes where each one acts as an individual ECL nano-emitter. This approach enables a change of paradigm by switching from a surface-limited process to 3D electrogenerated light emission.     

Cell membrane electropermeabilization by symmetrical bipolar rectangular pulses. Part II. Reduced electrolytic contamination

The paper presents a comparative study of the contamination of a cell suspension by ions released from aluminum cuvettes (Al(3+)) and stainless steel electrodes (Fe(2+)/Fe(3+)) during cell membrane electropermeabilization by unipolar and by symmetrical bipolar rectangular electric pulses. A single pulse and a train of eight pulses were delivered to electrodes at a 2-mm distance, with 100-micros and 1-ms pulse durations, and amplitudes ranging from 0 to 400 V for unipolar, and from 0 to 280 V for bipolar pulses. We found that the released concentrations of Al(3+) and Fe(2+)/Fe(3+) were always more than one order of magnitude lower with bipolar pulses than with unipolar pulses of the same amplitude and duration. We then investigated the viability of DC-3F cells after 1 h of incubation in the medium containing different concentrations of Al(3+) or Fe(2+)/Fe(3+) within the range of measured released concentrations (up to 2.5 mM for both ions), thus separating the effects of electrolytic contamination from the effects of electropermeabilization itself. For Fe(2+)/Fe(3+), loss of cell viability became significant at concentrations above 1.5 mM, while for Al(3+), no effect on cell survival was detected within the investigated range. Still, reports on the biochemical effects of released Al(3+) also suggest that with aluminum cuvettes, electrolytic contamination can be detrimental. Our study shows that electrolytic contamination and its detrimental effects can be largely reduced with no loss in efficiency of electropermeabilization, if bipolar rectangular pulses of the same amplitude and duration are used instead of the commonly applied unipolar pulses.     

Monopolar surfaces

Following the development of a methodology for determining the apolar components as well as the electron donor and the electron acceptor parameters of the surface tension of polar surfaces, surfaces of a number of quite common materials were found to manifest virtually only electron donor properties and no, or hardly, any electron acceptor properties. Such materials may be called monopolar; they can strongly interact with bipolar materials (e.g., with polar liquids such as water); but one single polar parameter of a monopolar material cannot contribute to its energy of cohesion. Monopolar materials manifesting only electron acceptor properties also may exist, but they do not appear to occur in as great an abundance. Among the electron donor monopolar materials are: polymethylmethacrylate, polyvinylalcohol, polyethyleneglycol, proteins, many polysaccharides, phospholipids, nonionic surfactants, cellulose esters, etc. Strongly monopolar materials of the same sign repel each other when immersed or dissolved in water or other polar liquids. The interfacial tension between strongly monopolar surfaces and water has a negative value. This leads to a tendency for water to penetrate between facing surfaces of a monopolar substance and hence, to repulsion between the molecules or particles of such a monopolar material, when immersed in water, and thus to pronounced solubility or dispersibility. Monopolar repulsion energies can far outweigh Lifshitz-van der Waals attractions as well as electrostatic and "steric" repulsions. In aqueous systems the commonly observed stabilization effects, which usually are ascribed to "steric" stabilization, may in many instances be attributed to monopolar repulsion between nonionic stabilizing molecules. The repulsion between monopolar molecules of the same sign can also lead to phase separation in aqueous solutions (or suspensions), where not only two, but multiple phases are possible. Negative interfacial tensions between monopolar surfactants and the brine phase can be the driving force for the formation of microemulsions; such negative interfacial tensions ultimately decay and stabilize at a value very close to zero. Strongly monopolar macromolecules or particles surrounded by oriented water molecules of hydration can still repel each other, albeit to an attenuated degree. This repulsion was earlier perceived as caused by "hydration pressure". A few of the relevant colloid and surface phenomena are reviewed and re-examined in the light of the influence of surface monopolarity on these phenomena.     

Magnetization Switching in the GdFeCo Films with In-Plane Anisotropy via Femtosecond Laser Pulses

Ferrimagnetic rare-earth substituted metal alloys GdFeCo were shown to exhibit the phenomenon of all-optical magnetization switching via femtosecond laser pulses. All-optical magnetization switching has been comprehensively investigated in out-of-plane magnetized GdFeCo films; however, the films with the in-plane magnetic anisotropy have not yet been studied in detail. We report experimental observations of the magnetization switching of in-plane magnetized GdFeCo films by means of the femtosecond laser pulses in the presence of a small magnetic field of about 40 µT. The switching effect has a threshold both in the applied magnetic field and in the light intensity.     

EXtended ACquisition Time (EXACT) NMR—A Case for ′Burst′ Non‐Uniform Sampling

A strong case exists for the introduction of burst non‐uniform sampling (NUS) in the direct dimension of NMR spectroscopy experiments. The resulting gaps in the NMR free induction decay can reduce the power demands of long experiments (by switching off broadband decoupling for example) and/or be used to introduce additional pulses (to refocus homonuclear coupling, for example). The final EXtended ACquisition Time (EXACT) spectra are accessed by algorithmic reconstruction of the missing data points and can provide higher resolution in the direct dimension than is achievable with existing non‐NUS methods.     

双极电极极化行为的模拟分析方法

在电化学工程中，常用一些具有三线结构的材料作为电极，如金属泡沫、碳纤维毡等．这种电极的优点是具有比平面（二维）电极大得多的电化学界面，常称三维电极·所谓双极三维电极是指在一种特殊状态下工作的三维电极：同一三维电极体的两侧分别发生阴极和阳极电极反应［‘，2］