- Award ID(s):
- 1907620
- Publication Date:
- NSF-PAR ID:
- 10285198
- Journal Name:
- Applicable Analysis
- Page Range or eLocation-ID:
- 1 to 20
- ISSN:
- 0003-6811
- Sponsoring Org:
- National Science Foundation
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The dynamics of initially truncated and bent line solitons for the Kadomtsev–Petviashvili (KPII) equation modelling internal and surface gravity waves is analysed using modulation theory. In contrast to previous studies on obliquely interacting solitons that develop from acute incidence angles, this work focuses on initial value problems for the obtuse incidence of two or three partial line solitons, which propagate away from one another. Despite counterpropagation, significant residual soliton interactions are observed with novel physical consequences. The initial value problem for a truncated line soliton – describing the emergence of a quasi-one-dimensional soliton from a wide channel – is shown to be related to the interaction of oblique solitons. Analytical descriptions for the development of weak and strong interactions are obtained in terms of interacting simple wave solutions of modulation equations for the local soliton amplitude and slope. In the weak interaction case, the long-time evolution of truncated and large obtuse angle solitons exhibits a decaying, parabolic wave profile with temporally increasing focal length that asymptotes to a cylindrical Korteweg–de Vries soliton. In contrast, the strong interaction case of slightly obtuse interacting solitons evolves into a steady, one-dimensional line soliton with amplitude reduced by an amount proportional to the incidencemore »
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Two-dimensional materials composed of transition metal carbides and nitrides (MXenes) are poised to revolutionize energy conversion and storage. In this work, we used density functional theory (DFT) to investigate the adsorption of Mg and Na adatoms on five M 2 CS 2 monolayers (where M = Mo, Nb, Ti, V, and Zr) for battery applications. We assessed the stability of the adatom ( i.e. Na and Mg)-monolayer systems by calculating adsorption and formation energies, as well as voltages as a function of surface coverage. For instance, we found that Mo 2 CS 2 cannot support a full layer of Na nor even a single Mg atom. Na and Mg exhibit the strongest binding on Zr 2 CS 2 , followed by Ti 2 CS 2 , Nb 2 CS 2 and V 2 CS 2 . Using the nudged elastic band method (NEB), we computed promising diffusion barriers for both dilute and nearly full ion surface coverage cases. In the dilute ion adsorption case, a single Mg and Na atom on Ti 2 CS 2 experience ∼0.47 eV and ∼0.10 eV diffusion barriers between the lowest energy sites, respectively. For a nearly full surface coverage, a Na ion moving onmore »
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We consider the time evolution in two spatial dimensions of a double vorticity layer consisting of two contiguous, infinite material fluid strips, each with uniform but generally differing vorticity, embedded in an otherwise infinite, irrotational, inviscid incompressible fluid. The potential application is to the wake dynamics formed by two boundary layers separating from a splitter plate. A thin-layer approximation is constructed where each layer thickness, measured normal to the common centre curve, is small in comparison with the local radius of curvature of the centre curve. The three-curve equations of contour dynamics that fully describe the double-layer dynamics are expanded in the small thickness parameter. At leading order, closed nonlinear initial-value evolution equations are obtained that describe the motion of the centre curve together with the time and spatial variation of each layer thickness. In the special case where the layer vorticities are equal, these equations reduce to the single-layer equation of Moore ( Stud. Appl. Math. , vol. 58, 1978, pp. 119–140). Analysis of the linear stability of the first-order equations to small-amplitude perturbations shows Kelvin–Helmholtz instability when the far-field fluid velocities on either side of the double layer are unequal. Equal velocities define a circulation-free double vorticity layer,more »
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