Phase field modeling of electrochemistry II: Kinetics

The kinetic behavior of a phase field model of electrochemistry is explored for advancing (electrodeposition) and receding (electrodissolution) conditions in one dimension. We described the equilibrium behavior of this model in [J. E. Guyer, W. J. Boettinger, J.A. Warren, and G. B. McFadden, ``Phase field modeling of electrochemistry I: Equilibrium'', cond-mat/0308173]. We examine the relationship between the parameters of the phase field method and the more typical parameters of electrochemistry. We demonstrate ohmic conduction in the electrode and ionic conduction in the electrolyte. We find that, despite making simple, linear dynamic postulates, we obtain the nonlinear relationship between current and overpotential predicted by the classical ``Butler-Volmer'' equation and observed in electrochemical experiments. The charge distribution in the interfacial double layer changes with the passage of current and, at sufficiently high currents, we find that the diffusion limited deposition of a more noble cation leads to alloy deposition with less noble species.Comment: v3: To be published in Phys. Rev. E v2: Attempt to work around turnpage bug. Replaced color Fig. 4a with grayscale 13 pages, 7 figures in 10 files, REVTeX 4, SIunits.sty, follows cond-mat/030817

A Model for Solid 3^3He: II

We propose a simple Ginzburg-Landau free energy to describe the magnetic phase transition in solid $^3$He. The free energy is analyzed with due consideration of the hard first order transitions at low magnetic fields. The resulting phase diagram contains all of the important features of the experimentally observed ph ase diagram. The free energy also yields a critical field at which the transition from the disordered state to the high field state changes from a first order to a second order one.Comment: This paper has been accepted for publication in Journal of Low Temperature Physics. Use regular Tex, with the D. Eardley version of Macros called jnl.tex. 10 pages, 4 figs available from [email protected]

Fluid Restriction Dehydration Increase Core Temperature During Endurance Exercise Compared to Exercise Induced Dehydration

International Journal of Exercise Science 15(2): 166-176, 2022. This study aimed to evaluate the difference in heart rate and core temperature during aerobic exercise between two forms of dehydration: exercise-induced (EI) and fluid restricted (FR). Twenty-two subjects (N = 22; 83.35 ± 13.92 kg) completed the current study, performing a familiarization session, a pre-experimental exercise session, and two exercise testing sessions. The EI exercise trial (81.52 ± 13.72 kg) was conducted after performing exercise in a hot environment to lose three to four percent of body weight and partial rehydration. The FR exercise trial (81.53 ± 14.14 kg) was completed after 12 hours of fluid restriction. During both exercise sessions, subjects pedaled against a set resistance of 130 watts for 30 minutes. The main effect of hydration on Tc was significant, F(1, 18) = 4.474, p = .049, ηp2 = .199 (Figure 2) with core temperature being greater during the FR trial compared to the EI trial (FR = 37.58 ± .06°C vs. EI = 37.31 ± .11°C). No significant interaction was found between hydration and time for HR, F(2, 42) = 0.120, p = .887, ηp2 = .006. The main effect of time on HR was significant, F(2, 42) = 119.664, p \u3c .001, ηp2 = .851. Fluid restriction was associated with an increase in core temperature. An increased core temperature may negatively influence performance, and care should be taken to ensure proper hydration

Phases of Josephson Junction Ladders

We study a Josephson junction ladder in a magnetic field in the absence of charging effects via a transfer matrix formalism. The eigenvalues of the transfer matrix are found numerically, giving a determination of the different phases of the ladder. The spatial periodicity of the ground state exhibits a devil's staircase as a function of the magnetic flux filling factor $f$. If the transverse Josephson coupling is varied a continuous superconducting-normal transition in the transverse direction is observed, analogous to the breakdown of the KAM trajectories in dynamical systems.Comment: 12 pages with 3 figures, REVTE

Driven Dynamics: A Probable Photodriven Frenkel-Kontorova Model

In this study, we examine the dynamics of a one-dimensional Frenkel-Kontorova chain consisting of nanosize clusters (the ''particles'') and photochromic molecules (the ''bonds''), and being subjected to a periodic substrate potential. Whether the whole chain should be running or be locked depends on both the frequency and the wavelength of the light (keeping the other parameters fixed), as observed through numerical simulation. In the locked state, the particles are bound at the bottom of the external potential and vibrate backwards and forwards at a constant amplitude. In the running state, the initially fed energy is transformed into directed motion as a whole. It is of interest to note that the driving energy is introduced to the system by the irradiation of light, and the driven mechanism is based on the dynamical competition between the inherent lengths of the moving object (the chain) and the supporting carrier (the isotropic surface). However, the most important is that the light-induced conformational changes of the chromophore lead to the time-and-space dependence of the rest lengths of the bonds.Comment: 4 pages,5 figure

Epitaxial growth in dislocation-free strained alloy films: Morphological and compositional instabilities

The mechanisms of stability or instability in the strained alloy film growth are of intense current interest to both theorists and experimentalists. We consider dislocation-free, coherent, growing alloy films which could exhibit a morphological instability without nucleation. We investigate such strained films by developing a nonequilibrium, continuum model and by performing a linear stability analysis. The couplings of film-substrate misfit strain, compositional stress, deposition rate, and growth temperature determine the stability of film morphology as well as the surface spinodal decomposition. We consider some realistic factors of epitaxial growth, in particular the composition dependence of elastic moduli and the coupling between top surface and underlying bulk of the film. The interplay of these factors leads to new stability results. In addition to the stability diagrams both above and below the coherent spinodal temperature, we also calculate the kinetic critical thickness for the onset of instability as well as its scaling behavior with respect to misfit strain and deposition rate. We apply our results to some real growth systems and discuss the implications related to some recent experimental observations.Comment: 26 pages, 13 eps figure

Resonant steps and spatiotemporal dynamics in the damped dc-driven Frenkel-Kontorova chain

Kink dynamics of the damped Frenkel-Kontorova (discrete sine-Gordon) chain driven by a constant external force are investigated. Resonant steplike transitions of the average velocity occur due to the competitions between the moving kinks and their radiated phasonlike modes. A mean-field consideration is introduced to give a precise prediction of the resonant steps. Slip-stick motion and spatiotemporal dynamics on those resonant steps are discussed. Our results can be applied to studies of the fluxon dynamics of 1D Josephson-junction arrays and ladders, dislocations, tribology and other fields.Comment: 20 Plain Latex pages, 10 Eps figures, to appear in Phys. Rev.

Phase field modeling of electrochemistry I: Equilibrium

A diffuse interface (phase field) model for an electrochemical system is developed. We describe the minimal set of components needed to model an electrochemical interface and present a variational derivation of the governing equations. With a simple set of assumptions: mass and volume constraints, Poisson's equation, ideal solution thermodynamics in the bulk, and a simple description of the competing energies in the interface, the model captures the charge separation associated with the equilibrium double layer at the electrochemical interface. The decay of the electrostatic potential in the electrolyte agrees with the classical Gouy-Chapman and Debye-H\"uckel theories. We calculate the surface energy, surface charge, and differential capacitance as functions of potential and find qualitative agreement between the model and existing theories and experiments. In particular, the differential capacitance curves exhibit complex shapes with multiple extrema, as exhibited in many electrochemical systems.Comment: v3: To be published in Phys. Rev. E v2: Added link to cond-mat/0308179 in References 13 pages, 6 figures in 15 files, REVTeX 4, SIUnits.sty. Precedes cond-mat/030817