Modeling power grids
We present a method to construct random model power grids that closely match statistical properties of a real power grid. The model grids are more difficult to partition than a real grid.
physics.soc-ph↗
arXiv subjects
I. Abou Hamad
Publications and source records attributed to I. Abou Hamad.
A New Charging Method for Li-ion Batteries: Dependence of the charging time on the Direction of an Additional Oscillating Field
We have recently proposed a new method for charging Li-ion batteries based on large-scale molecular dynamics studies (I. Abou Hamad et al, Phys. Chem. Chem. Phys., 12, 2740 (2010)). Applying an additional oscillating electric field in the direction perpendicular to the graphite sheets of the anode showed an exponential decrease in charging time with increasing amplitude of the applied oscillating field. Here we present new results exploring the effect on the charging time of changing the orientation of the oscillating field. Results for oscillating fields in three orthogonal directions are compared.
physics.chem-ph↗
Applications of Computer Simulations and Statistical Mechanics in Surface Electrochemistry
We present a brief survey of methods that utilize computer simulations and quantum and statistical mechanics in the analysis of electrochemical systems. The methods, Molecular Dynamics and Monte Carlo simulations and quantum-mechanical density-functional theory, are illustrated with examples from simulations of lithium-battery charging and electrochemical adsorption of bromine on single-crystal silver electrodes.
physics.chem-ph↗
New Cyclic Voltammetry Method for Examining Phase Transitions: Simulated Results
We propose a new experimental technique for cyclic voltammetry, based on the first-order reversal curve (FORC) method for analysis of systems undergoing hysteresis. The advantages of this electrochemical FORC (EC-FORC) technique are demonstrated by applying it to dynamical models of electrochemical adsorption. The method can not only differentiate between discontinuous and continuous phase transitions, but can also quite accurately recover equilibrium behavior from dynamic analysis of systems with a continuous phase transition. Experimental data for EC-FORC analysis could easily be obtained by simple reprogramming of a potentiostat designed for conventional cyclic-voltammetry experiments.
cond-mat.mtrl-sci↗
First-order Reversal Curve Analysis of Phase Transitions in Electrochemical Adsorption: A New Experimental Technique Suggested by Computer Simulations
The first-order reversal curve (FORC) method for analysis of systems undergoing hysteresis is applied to dynamical models of electrochemical adsorption. In this setting, the method can not only differentiate between discontinuous and continuous phase transitions, but can also quite accurately recover equilibrium behavior from dynamic analysis for systems with a continuous phase transition. Discontinuous and continuous phase transitions in a two-dimensional lattice-gas model are compared using the FORC method. The FORC diagram for a discontinuous phase transition is characterized by a negative (unstable) region separating two positive (stable) regions, while such a negative region does not exist for continuous phase transitions. Experimental data for FORC analysis could easily be obtained by simple reprogramming of a potentiostat designed for cyclic-voltammetry experiments.
cond-mat.mtrl-sci↗
Reply to ``Remarks on the simulation of Cl electrosorption on Ag(100) reported in Electrochimica Acta 50 (2005) 5518"
We reply to remarks by Lang and Horanyi on the meaning of the notion of "electrosorption valency" used in I. Abou Hamad et al., Electrochim. Acta 50 (2005) 5518. It is concluded that, contrary to the assertion of Lang and Horanyi, the magnitude of the current in the external circuit upon adsorption of an ion of charge ze with partial charge transfer is indeed given by an electrosorption valency gamma such that |gamma e| < |ze|. We believe the conclusion of Lang and Horanyi to the contrary is the result of an excessively severe charge-neutrality requirement.
physics.chem-ph↗
Cl electrosorption on Ag(100): Lateral interactions and electrosorption valency from comparison of Monte Carlo simulations with chronocoulometry experiments
We present Monte Carlo Simulations using an equilibrium lattice-gas model for the electrosorption of Cl on Ag(100) single-crystal surfaces. Fitting the simulated isotherms to chronocoulometry experiments, we extract parameters such as the electrosorption valency gamma and the next-nearest-neighbor lateral interaction energy phi_nnn. Both coverage-dependent and coverage independent gamma were previously studied assuming a constant phi_nnn [I. Abou Hamad, Th. Wandlowski, G. Brown, P.A. Rikvold, J. Electroanal. Chem. 554-555 (2003) 211]. Here, a self-consistent, entirely electrostatic picture of the lateral interactions with a coverage-dependent phi_nnn is developed, and a relationship between phi_nnn and gamma is investigated for Cl on Ag(100).
cond-mat.mtrl-sci↗
Determination of the basic timescale in kinetic Monte Carlo simulations by comparison with cyclic-voltammetry experiments
While kinetic Monte Carlo simulations can provide long-time simulations of the dynamics of physical and chemical systems, it is not yet possible in general to identify the inverse Monte Carlo attempt frequency with a physical timescale. Here we demonstrate such an identification by comparing simulations with experimental data. Using a dynamic lattice-gas model for the electrosorption of Br on Ag(100), we measure the scan-rate dependence of the separation between positive-and negative-going peaks in cyclic-voltammetry (CV) and compare simulated and experimental peak separations. By adjusting the Monte Carlo attempt frequency, good agreement between simulated and experimental peak separations is achieved. It is also found that the uniqueness of such a determination is dependent on the relative values of the adsorption/desorption and diffusion free-energy barriers.
cond-mat.mtrl-sci↗
Electrosorption of Br and Cl on Ag(100): Experiments and Computer Simulations
We present chronocoulometry experiments and equilibrium Monte Carlo simulations for the electrosorption of Br and Cl on Ag(100) single-crystal electrode surfaces. Two different methods are used to calculate the long-range part of the adsorbate-adsorbate interactions. The first method is a truncated-sum approach, while the second is a mean-field-enhanced truncated-sum approach. To compare the two methods, the resulting isotherms are fit to experimental adsorption isotherms, assuming both a constant electrosorption valency &gamma and also a coverage-dependent &gamma. While a constant &gamma fits the Br/Ag(100) well, a coverage-dependent or potential-dependent &gamma is needed for Cl/Ag(100).
cond-mat.mtrl-sci↗