scholarly journals Polyelectrolytes induce water-water correlations that result in dramatic viscosity changes and nuclear quantum effects

2019 ◽  
Vol 5 (12) ◽  
pp. eaay1443 ◽  
Author(s):  
J. Dedic ◽  
H. I. Okur ◽  
S. Roke

Ions interact with water via short-ranged ion-dipole interactions. Recently, an additional unexpected long-ranged interaction was found: The total electric field of ions influences water-water correlations over tens of hydration shells, leading to the Jones Ray effect, a 0.3% surface tension depression. Here, we report such long-range interactions contributing substantially to both molecular and macroscopic properties. Femtosecond elastic second harmonic scattering (fs-ESHS) shows that long-range electrostatic interactions are remarkably strong in aqueous polyelectrolyte solutions, leading to an increase in water-water correlations. This increase plays a role in the reduced viscosity, which changes more than two orders of magnitude with polyelectrolyte concentration. Using D2O instead of H2O shifts both the fs-ESHS and the viscosity curve by a factor of ~10 and reduces the maximum viscosity value by 20 to 300%, depending on the polyelectrolyte. These phenomena cannot be explained using a mean-field approximation of the solvent and point to nuclear quantum effects.

2021 ◽  
Author(s):  
Jonas Landsgesell ◽  
David Beyer ◽  
Pascal Hebbeker ◽  
Peter Košovan ◽  
Christian Holm

The swelling of polyelectrolyte hydrogels has been often explained using simple models derived from the Flory-Rehner model. While these models qualitatively predict the experimentally observed trends, they also introduce strong approximations and neglect some important contributions. Consequently, they sometimes incorrectly ascribe the observed trends to contributions which are of minor importance under the given conditions. In this work, we investigate the swelling properties of weak (pH-responsive) polyelectrolyte gels at various pH and salt concentrations, using a hierarchy of models, gradually introducing various approximations. For the first time, we introduce a three-dimensional particle-based model which accounts for the topology of the hydrogel network, for electrostatic interactions between gel segments and small ions and for acid-base equilibrium coupled to the Donnan partitioning of small ions. This model is the most accurate one, therefore, we use it as a reference when assessing the effect of various approximations. As the first approximation, we introduce the affine deformation, which allows us to replace the network of many chains by a single chain, while retaining the particle-based representation. In the next step, we use the mean-field approximation to replace particles by density fields, combining the Poisson-Boltzmann equation with elastic stretching of the chain. Finally, we introduce an ideal gel model by neglecting the electrostatics while retaining all other features of the previous model. Comparing predictions from all four models allows us to understand which contributions dominate at high or low pH or salt concentrations. We observe that the field-based models overestimate the ionization degree of the gel because they underestimate the electrostatic interactions. Nevertheless, a cancellation of effects on the electrostatic interactions and Donnan partitioning causes that both particle-based and field-based models consistently predict the swelling of the gels as a function of pH and salt concentration. Thus, we can conclude that any of the employed models can rationalize the known experimental trends in gel swelling, however, only the particle-based models fully account for the true effects causing these trends. The full understanding of differences between various models is important when interpreting experimental results in the framework of existing theories and for ascribing the observed trends to particular contributions, such as the Donnan partitioning of ions, osmotic pressure or electrostatic interactions.


1992 ◽  
Vol 06 (20) ◽  
pp. 3327-3340 ◽  
Author(s):  
PAVOL KALINAY

Having treated the t-J Hamiltonian in the mean-field approximation on basis generated by the Hubbard operators [Formula: see text], we tried to find the superconductive phase on the antiferromagnetic background. The pairing of the d-wave symmetry appeared to coexist well with the AF long-range order.


2013 ◽  
Vol 58 (4) ◽  
pp. 1401-1403 ◽  
Author(s):  
J.A. Bartkowska ◽  
R. Zachariasz ◽  
D. Bochenek ◽  
J. Ilczuk

Abstract In the present work, the magnetoelectric coupling coefficient, from the temperature dependences of the dielectric permittivity for the multiferroic composite was determined. The research material was ferroelectric-ferromagnetic composite on the based PZT and ferrite. We investigated the temperature dependences of the dielectric permittivity (") for the different frequency of measurement’s field. From the dielectric measurements we determined the temperature of phase transition from ferroelectric to paraelectric phase. For the theoretical description of the temperature dependence of the dielectric constant, the Hamiltonian of Alcantara, Gehring and Janssen was used. To investigate the dielectric properties of the multiferroic composite this Hamiltonian was expressed under the mean-field approximation. Based on dielectric measurements and theoretical considerations, the values of the magnetoelectric coupling coefficient were specified.


2021 ◽  
Vol 7 (10) ◽  
pp. eabf2558
Author(s):  
J. Dedic ◽  
H. I. Okur ◽  
S. Roke

Hyaluronan (HA) is an anionic, highly hydrated bio-polyelectrolyte found in the extracellular environment, like the synovial fluid between joints. We explore the extended hydration shell structure of HA in water using femtosecond elastic second-harmonic scattering (fs-ESHS). HA enhances orientational water-water correlations. Angle-resolved fs-ESHS measurements and nonlinear optical modeling show that HA behaves like a flexible chain surrounded by extended shells of orientationally correlated water. We describe several ways to determine the concentration-dependent size and shape of a polyelectrolyte in water, using the amount of water oriented by the polyelectrolyte charges as a contrast agent. The spatial extent of the hydration shell is determined via temperature-dependent measurements and can reach up to 475 nm, corresponding to a length of 1600 water molecules. A strong isotope effect, stemming from nuclear quantum effects, is observed when light water (H2O) is replaced by heavy water (D2O), amounting to a factor of 4.3 in the scattered SH intensity.


2021 ◽  
Vol 7 (5) ◽  
pp. 69
Author(s):  
Catherine Cazelles ◽  
Jorge Linares ◽  
Mamadou Ndiaye ◽  
Pierre-Richard Dahoo ◽  
Kamel Boukheddaden

The properties of spin crossover (SCO) nanoparticles were studied for five 2D hexagonal lattice structures of increasing sizes embedded in a matrix, thus affecting the thermal properties of the SCO region. These effects were modeled using the Ising-like model in the framework of local mean field approximation (LMFA). The systematic combined effect of the different types of couplings, consisting of (i) bulk short- and long-range interactions and (ii) edge and corner interactions at the surface mediated by the matrix environment, were investigated by using parameter values typical of SCO complexes. Gradual two and three hysteretic transition curves from the LS to HS states were obtained. The results were interpreted in terms of the competition between the structure-dependent order and disorder temperatures (TO.D.) of internal coupling origin and the ligand field-dependent equilibrium temperatures (Teq) of external origin.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Huziel E. Sauceda ◽  
Valentin Vassilev-Galindo ◽  
Stefan Chmiela ◽  
Klaus-Robert Müller ◽  
Alexandre Tkatchenko

AbstractNuclear quantum effects (NQE) tend to generate delocalized molecular dynamics due to the inclusion of the zero point energy and its coupling with the anharmonicities in interatomic interactions. Here, we present evidence that NQE often enhance electronic interactions and, in turn, can result in dynamical molecular stabilization at finite temperature. The underlying physical mechanism promoted by NQE depends on the particular interaction under consideration. First, the effective reduction of interatomic distances between functional groups within a molecule can enhance the n → π* interaction by increasing the overlap between molecular orbitals or by strengthening electrostatic interactions between neighboring charge densities. Second, NQE can localize methyl rotors by temporarily changing molecular bond orders and leading to the emergence of localized transient rotor states. Third, for noncovalent van der Waals interactions the strengthening comes from the increase of the polarizability given the expanded average interatomic distances induced by NQE. The implications of these boosted interactions include counterintuitive hydroxyl–hydroxyl bonding, hindered methyl rotor dynamics, and molecular stiffening which generates smoother free-energy surfaces. Our findings yield new insights into the versatile role of nuclear quantum fluctuations in molecules and materials.


1997 ◽  
Vol 11 (20) ◽  
pp. 867-875 ◽  
Author(s):  
A. A. Rodríaguez ◽  
E. Medina

We study novel geometrical and transport properties of a 2D model of disordered fibre networks. To assess the geometrical structure we determine, analytically, the probability distribution for the number of fibre intersections and resulting segment sizes in the network as a function of fibre density and length. We also determine, numerically, the probability distribution of pore perimeters and areas. We find a non-monotonous behavior of the perimeter distribution whose main features can be explained by solving for two simplified models of the line network. Finally we formulate a mean field approximation to conduction, above the percolation threshold, using the derived results. Relevance of the results to fracture networks will be discussed.


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