The surface of a polar liquid presents a special environment for the solvation and organization of charged solutes, which differ from bulk behaviors in important ways. These differences have motivated many attempts to understand electrostatic response at aqueous interfaces in terms of a spatially varying dielectric permittivity, typically concluding that the dielectric constant of interfacial water is significantly lower than in the bulk liquid. Such analyses, however, are complicated by the potentially nonlocal nature of dielectric response over the short length scales of interfacial heterogeneity. Here we circumvent this problem for thin water films by adopting a thermodynamic approach. Using molecular simulations, we calculate the solvent's contribution to the reversible work of charging a parallel plate capacitor. We find good agreement with a simple dielectric continuum model that assumes bulk dielectric permittivity all the way up to the liquid's boundary, even for very thin ($\sim 1$ nm) films. This comparison requires careful attention to the placement of dielectric boundaries between liquid and vapor, which also resolves apparent discrepancies with dielectric imaging experiments.
Investigations of dielectric properties of water in nanoconfinement are highly relevant for various applications. Here, using a simple capacitor model, we show that the low dielectric constant of nanoconfined water found in molecular dynamics simulations can be largely explained by the so-called dielectric dead-layer effect known for ferroelectric nanocapacitors.
One century ago pioneering dielectric results obtained for water and n-alcohols triggered the advent of molecular rotation diffusion theory considered by Debye to describe the primary dielectric absorption in these liquids. Comparing dielectric, viscoelastic, and light scattering results we unambiguously demonstrate that the structural relaxation appears only as a high-frequency shoulder in the dielectric spectra of water. In contrast, the main dielectric peak is related to a supramolecular structure, analogous to the Debye-like peak observed in mono-alcohols.
We define the dielectric constant (susceptibility) that should enter the Maxwell boundary value problem when applied to microscopic dielectric interfaces. The dielectric constant (susceptibility) of the interface is defined by exact linear-response equations involving correlations of statistically fluctuating interface polarization and the Coulomb interaction energy of external charges with the dielectric. The theory is applied to the interface between water and spherical solutes of altering size studied by molecular dynamics (MD) simulations. The effective dielectric constant of interfacial w…
In this work, the dielectric behavior of water inside charged nanoslit of graphene is studied to analized the water molecules under electrical confinement; through polarizing the nanoslit of graphene, creating an electric field inside the nanopore. How the water molecules are structured under this type of electrical confinement is studied with two force fields of water, the three-site water models here used are the SCP/$ε$ and the FAB/$ε$, the first is a rigid model that improves the SPC model and the second is a flexible model that improves all the force fields of three sites non-polarizables…
The inter-connection between the elasticity of a dielectric film and the wetting of a sessile drop on the same, under an applied electrical voltage, remains unaddressed. Here, we report the electrowetting-on-dielectric (EWOD) behaviour of sessile drops on dielectric elastomer films of varying elasticities- from an apparently rigid dielectric film to a soft, deformable dielectric film. Our results reveal that the elasticity of the underlying dielectric film provides an additional control over the droplet electrowetting behaviour, which may be best addressed from free energy based consideration,…
High temperature polymeric materials for electrical insulation and energy storage are needed for transformational power applications such as pulsed-power and hyrid electrical vehicles. One of the candidate materials has been polyetherimide, an amourphous thermoplastic with a glass transition over 200C. Here dielectric studies on the material are reported by taking into account the polarization and conduction processes in the polyetherimide.
Dielectric permittivity of supercooled volume water has been measured in the range of temperatures from $-20\,^{\circ}$C to $-60\,^{\circ}$C at the frequencies $7.6$~GHz and $9.7$~GHz. The measurements have been made using microwave resonators and wetted silicate sorbents. From the data obtained, the temperature dependences of the relaxation frequencies were updated for the Debye model with two relaxation frequencies. The updated formulae for dielectric permittivity of cold water may be applied to the frequency range $7\ldots200$~GHz.
Recent experiments reporting a very low dielectric permittivity for nanoconfined water have renewed the interest to the structure and dielectric properties of water in narrow gaps. Here, we describe such systems with a minimal Landau-Ginzburg field-theory composed of a nonlocal bulk-determined term and a local water-surface interaction term. We show how the interplay between the boundary conditions and intrinsic bulk correlations encodes dielectric properties of confined water. Our theoretical analysis is supported by molecular dynamics simulations and comparison with the experimental data.
The dielectric relaxation of water in glassy aqueous binary mixtures exhibits an Arrhenius behaviour with a nearly universal activation energy. We here demonstrate that its characteristic relaxation time follows a remarkably general functional dependence on the weight fraction of water for a wide range of molecular systems.
We investigate the temperature dependence of thermodynamic (density, isobaric heat capacity), dynamical (self-diffusion coefficient, shear viscosity), and dielectric properties of several water models, the commonly employed TIP3P water model, well-established 4-point water model TIP4P-2005, and recently developed 4-point water model TIP4P-D. We focus on the temperature range of interest for the field of computational biophysics and soft matter (280-350 K). The 4-point water models lead to a spectacularly improved agreement with experimental data, strongly suggesting that the use of more modern…
The glass transition temperature $T_{\rm g}$ and the temperature $T_α$ corresponding to the peak in the dielectric loss due to the $α$-process have been simultaneously determined as functions of film thickness d through dielectric measurements for polystyrene thin films supported on glass substrate. The dielectric loss peaks have also been investigated as functions of frequency for a given temperature. A decrease in $T_{\rm g}$ was observed with decreasing film thickness, while $T_α$ was found to remain almost constant for $d>d_{\rm c}$ and to decrease drastically with decreasing d for $d<d_{\…
Dielectric relaxation and thermal expansion spectroscopy were made for thin polystyrene films in order to measure the temperature $T_α$ corresponding to the peak in the loss component of susceptibility due to the $α$-process and the $α$-relaxation time $τ$ as functions of film thickness $d$. While the glass transition temperature $T_{\rm g}$ decreases with decreasing film thickness, $T_α$ and $τ$ were found to remain almost constant for $d>d_{\rm c}$ and decrease drastically for $d<d_{\rm c}$ for high temperatures. Here, $d_{\rm c}$ is a critical thickness. Near the glass transition temperatur…
In this work we give the analysis of the low frequency dielectric response of selected kaolinitic clays at different water content ranging from dry, over plastic to liquid limit. For all samples investigated, depending on the moisture content, the real part of the dielectric function reflects the abnormal behaviour within the certain frequency region where the negative values of real part of dielectric response have been observed. The anomalies are explained within a generalized conductivity model based on the clay-water electrolyte ions free motion in pore water and their restricted motion ne…
We present a theoretical calculation of the changes in the Hamaker constant due to the anomalous reduction of the static dielectric function of water. Under confinement, the dielectric function of water decreases from a bulk value of 79 down to 2. If the confining walls are made of a dielectric material, the Hamaker constant reduces almost by 90\%. However, if the confinement is realized with metallic plates, there is little change in the Hamaker constant. Additionally, we show that confinement can be used to decreases the Debye screening length without changing the salt concentration. This, i…
The static dielectric constant of liquid water is computed using classical force field based molecular dynamics simulation at fixed electric displacement D. The method to constrain the electric displacement is the finite temperature classical variant of the constant-D method developed by Stengel, Spaldin and Vanderbilt (Nat. Phys. 2009, 5: 304). There is also a modification of this scheme imposing fixed values of the macroscopic field E. The method is applied to the popular SPC/E model of liquid water. We compare four different estimates of the dielectric constant, two obtained from fluctuatio…
Unambiguous characterization of in-plane dielectric response in nanoconfined liquids: water as a case study
Donostia International Physics Center (DIPC)（多诺西亚国际物理中心）；Department of Applied Physics, Engineering School of Gipuzkoa, Basque Country University, UPV/EHU（巴斯克地区大学工程学校吉普斯夸应用物理系）
Soft elastomers that can exhibit extremely large deformations under the action of an electric field are essential for applications such as soft robotics, stretchable and flexible electronics, energy harvesting among others. The critical limiting factor in conventional electro-actuation of such materials is the occurrence of the so-called pull-in instability. In this work, we demonstrate an extraordinarily simple way to coax a dielectric thin film towards a symmetry-breaking pitchfork bifurcation state while avoiding pull-in instability. Through the nonlinear interplay between the two bifurcati…
Dipolar susceptibility of interfacial water and the corresponding interface dielectric constant were calculated from numerical molecular dynamics simulations for neutral and charged states of buckminsterfullerene C$_{60}$. Dielectric constants in the range 10--22, depending on temperature and solute charge, were found. The hydration water undergoes a structural crossover as a function of the solute charge. Its main signatures include the release of dangling O-H bonds pointing toward the solute and the change in the preferential orientations of hydration water from those characterizing hydropho…
The performances of energy harvesting generators based on dielectric elastomers are investigated. The configuration is of a thin dielectric film coated by stretchable electrodes at both sides. The film is first stretched, then charged and subsequently, afterwards it is released, and finally the charge is harvested at a higher electric potential. The amount of energy extracted by this cycle is bounded by the electric breakdown and the ultimate stretch ratio of the film as well as by structural instabilities due to loss of tension. To identify the optimal cycle that complies with these limits we…
Despite water is the most studied substance in the Earth, it is not completely understood why its structural and dynamical properties give rise to some anomalous behaviors. Interesting properties emerge when experiments at low temperatures and/or high pressures, are performed. Here we report dielectric measurements of cold water under constrained conditions, i.e. water that below the melting point can not freeze. The inner pressure shifts the α relaxation peak to similar frequencies as seen in ice Ih. Also, when we reach the triple point at 251 K, ice III seems to form. As far as we know, this…
The goal of this work is to propose a simple continuous model that captures the dielectric properties of water at the nanometric scale. We write an electrostatic energy as a functional of the polarisation field containing a term in $P^4$ and non-local Gaussian terms. Such an hamiltonian can reproduce two key properties of water: the saturation of the polarisation response of water in the presence of a strong electrostatic field and the nanometric dipolar correlations of the solvent molecules modifying the long range van der waals interaction. This model explores thus two fundamental aspects th…
Inks of permanent markers and water-proof cosmetics create elastic thin films upon application on a surface. Such adhesive materials are deliberately designed to exhibit water-repellent behavior. Therefore, patterns made up of these inks become resistant to moisture and cannot be cleaned by water after drying. However, we show that sufficiently slow dipping of such elastic films, which are adhered to a substrate, into a bath of pure water allows complete removal of the hydrophobic coatings. Upon dipping, the air-water interface in the bath forms a contact line on the substrate, which exerts a …
Glassy dynamics was investigated for thin films of atactic polystyrene by complex electric capacitance measurements using dielectric relaxation spectroscopy. During the isothermal aging process the real part of the electric capacitance increased with time, whereas the imaginary part decreased with time. It follows that the aging time dependences of real and imaginary parts of the electric capacitance were primarily associated with change in volume (film thickness) and dielectric permittivity, respectively. Further, dielectric permittivity showed memory and rejuvenation effects in a similar man…
Isothermal-isobaric molecular dynamics simulations have been performed to examine an ample set of properties of the model water-N,N-dimethylformamide (DMF) mixture as a function of composition. The SPC-E and TIP4P-Ew water models together with two united atom models for DMF [Chalaris M., Samios J., J. Chem. Phys., 2000, 112, 8581; Cordeiro J., Int. J. Quantum Chem., 1997, 65, 709] were used. Our principal analyses concern the behaviour of structural properties in terms of radial distribution functions, and the number of hydrogen bonds between molecules of different species as well as thermodyn…
Gigahertz-to-terahertz spectroscopy of macromolecules in aqueous environments provides an important approach for identifying their global and transient molecular structures, as well as directly assessing hydrogen-bonding. We report dielectric properties of zwitterionic dodecylphosphocholine (DPC) micelles in aqueous solutions over a wide frequency range, from 50 MHz to 1.12 THz. The dielectric relaxation spectra reveal different polarization mechanisms at the molecular level, reflecting the complexity of DPC micelle-water interactions. We have made a deconvolution of the spectra into different…
We present an accurate free-energy functional for liquid water written in terms of a set of effective potential fields in which fictitious noninteracting water molecules move. The functional contains an \emph{exact} expression of the entropy of noninteracting molecules and thus provides an ideal starting point for the inclusion of complex inter-molecular interactions which depend on the \emph{orientation} of the interacting molecules. We show how an excess free-energy functional can be constructed to reproduce the following properties of water: the dielectric response; the experimental site-si…
We have investigated thermodynamic and dynamic properties as well as the dielectric constant of water-metha\-nol model mixtures in the entire range of composition by using constant pressure molecular dynamics simulations at ambient conditions. The SPC/E and TIP4P/Ew water models are used in combination with the OPLS united atom modelling for methanol. Changes of the average number of hydrogen bonds between particles of different species and of the fractions of differently bonded molecules are put in correspondence with the behavior of excess mixing volume and enthalpy, of self-diffusion coeffi…
We present a critical comparison of the dielectric properties of three models of water - TIP4P/2005, TIP4P/2005f and TTM3F. Dipole spatial correlation is measured using the distance dependent Kirkwood function along with one dimensional and two dimensional dipole correlation functions. We find that the introduction of flexibility alone does not significantly affect dipole correlation and only affects $\varepsilon(ω)$ at high frequencies. By contrast the introduction of polarizability increases dipole correlation and yields a more accurate $\varepsilon(ω)$. Additionally the introduction of pola…
We generalize the predictions for attractions between over-all neutral surfaces induced by charge fluctuations/correlations to non-uniform systems that include dielectric discontinuities, as is the case for mixed charged lipid membranes in an aqueous solution. We show that the induced interactions depend in a non-trivial way on the dielectric constants of membrane and water and show different scaling with distance depending on these properties. The generality of the calculations also allows us to predict under which dielectric conditions the interaction will change sign and become repulsive.
Dielectric spectra (10^4-10^11 Hz) of water and ice at 0 °C are considered in terms of proton conductivity and compared to each other. In this picture, the Debye relaxations, centered at 1/τ_W ~ 20 GHz (in water) and 1/τ_I ~ 5 kHz (in ice), are seen as manifestations of diffusion of separated charges in the form of H3O+ and OH- ions. The charge separation results from the self-dissociation of H2O molecules, and is accompanied by recombination in order to maintain the equilibrium concentration, N. The charge recombination is a diffusion-controlled process with characteristic lifetimes of τ_W an…
We investigate the relaxation behavior of thin films of a polyamide random copolymer, PA66/6I, with various film thicknesses using dielectric relaxation spectroscopy. Two dielectric signals are observed at high temperatures, the $α$-process and the relaxation process due to electrode polarization (the EP-process). The relaxation time of the EP-process has a Vogel-Fulcher-Tammann type of temperature dependence, and the glass transition temperature, $T_{\rm g}$, evaluated from the EP-process agrees very well with the $T_{\rm g}$ determined from the thermal measurements. The fragility index deriv…
Isotopic Fingerprints of Proton-mediated Dielectric Relaxation in Solid and Liquid Water
Austrian Institute of Technology（奥地利技术研究所）；Israel Institute of Technology（以色列理工学院）；University of Washington（华盛顿大学）；École Polytechnique Fédérale de Lausanne（洛桑联邦理工学院）；Hamburg University of Technology（汉堡工业大学）
The Infrared Spectrum is used as an experimental data target, to improved the TIP4P/$ε$, adding harmonic potential U(r) in all bonds and harmonic potential U(θ) in the angle formed by the hydrogens and oxygen atoms of the water molecule. The flexibility in the molecule gives the ability of the water molecules to change, around different temperatures and pressures, their structure and in the bulk liquid the distribution of the dipole moment. This distribution helps to reproduce better the experimental data that the rigid models can not describe. The rigid water models of 3 and 4 sites have limi…
Accurate and integrable control of different flows within microfluidic channels is crucial to further development of lab-on-a-chip and fully integrated adaptable structures. Here we introduce a flexible microactuator that buckles at a high deformation rate and alters the downstream fluid flow. The microactuator consists of a confined, thin, dielectric film that buckles into the microfluidic channel when exposed to voltage supplied through conductive fluid electrodes. We estimate the critical buckling voltage, and characterize the buckled shape of the actuator. Finally, we investigate the effec…
The effect of the applied trajectory length on the convergence of the static dielectric constant and the self-diffusion coefficient were examined for the SPC/E water model in the NVT ensemble with different system size at 293 K. Very long simulation times of 6-8 ns were employed in order to track the convergence of these properties. Temperature dependence and isotope effects, via using D$_2$O instead of H$_2$O, were also investigated. A simulation for the polarizable SWM4-DP model was also carried out to compare the effect of different potential models. Radial distribution functions and the ne…
In spite of a large number of papers published in the last twenty years in the literature, the basic model of liquid water is still controversial. We have measured the dielectric permittivity of pure water and aqueous chlorides solutions in the range 0.2 to 1.5 THz and we have found that the overall dielectric behavior can be satisfactorily described with the weighted average of two single time constant Debye functions. The weights of the two components have been obtained by infrared spectra analysis and are related to two populations of water molecules having a different long range organizati…
We demonstrate that Casimir-Polder energies between noble gas atoms (dissolved in water) and oil-water interfaces are highly surface specific. Both repulsion (e.g. hexane) and attraction (e.g. glycerine and cyclodecane) is found with different oils. For several intermediate oils (e.g. hexadecane, decane, and cyclohexane) both attraction and repulsion can be found in the same system. Near these oil-water interfaces the interaction is repulsive in the non-retarded limit and turns attractive at larger distances as retardation becomes important. These highly surface specific interactions may have …
We have employed molecular dynamics simulations based on the TIP4P/2005 water model to investigate the local structural, dynamical, and dielectric properties of the two recently reported body-centered-cubic and face-centered-cubic plastic crystal phases of water. Our results reveal significant differences in the local orientational structure and rotational dynamics of water molecules for the two polymorphs. The probability distributions of trigonal and tetrahedral order parameters exhibit a multi-modal structure, implying the existence of significant local orientational heterogeneities, partic…
The mechanical properties of nanoconfined water layers are still poorly understood and continue to create considerable controversy, despite their importance for biology and nanotechnology. Here, we report on dynamic nanomechanical measurements of water films compressed down to a few single molecular layers. We show that the mechanical properties of nanoconfined water layers change dramatically with their dynamic state. In particular, we observed a sharp transition from viscous to elastic response even at extremely slow compression rates, indicating that mechanical relaxation times increase dra…
We report on electrically-induced rotations in water films, which can function at many length scales. The device consists of a two-dimensional cell used for electrolysis of water films, as simple as an insulator frame with two electrodes on the sides, to which an external in-plane electric field perpendicular to the mean electrolysis current density is applied. If either the external field or the electrolysis current exceeds some threshold (while the other one is not zero), the liquid film begins to rotate.
We studied dielectric properties of nano-sized liquid water samples confined in polymerized silicates MCM-41 characterized by the porous sizes \sim 3-10nm. We report the direct measurements of the dielectric constant by the dielectric spectroscopy method at frequencies 25Hz-1MHz and demonstrate clear signatures of the second-order phase transition of ferroelectric nature at temperatures next to the λ- point in the bulk supercooled water. The presented results support the previously developed polar liquid phenomenology and hence establish its applicability to model actual phenomena in liquid wa…
