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Molecular Dynamics Simulations of Reverse Osmosis in Silica Nanopores
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An Ab Initio -Derived Force Field for Amorphous Silica Interfaces for Use in Molecular Dynamics Simulations
Here, we present a classical interatomic force field, silica-DDEC, to describe the interactions of amorphous and crystalline silica surfaces, parametrized using density functional theory-based charges. Charge schemes for silica surfaces were developed using the density-derived electrostatic and chemical (DDEC) method, which reproduces atomic charges of the periodic models as well as the electrostatic potential away from the atom sites. Lennard–Jones parameters were determined by requiring the correct description of (i) the amorphous silica density, coordination defects, and local coordination geometry, relative to experimental measurements, and (ii) water-silica interatomic distances compared with ab initio results. Deprotonated surface silanol sites are also described within the model based on DDEC charges. The result is a general electronic structure-derived model for describing fully flexible amorphous and crystalline silica surfaces and interactions of liquids with silica surfaces of varying structure and protonation state.
Properties of Erythritol Tetranitrate from Molecular Dynamics Simulation
Not Available
Sum Frequency Generation Spectroscopy and Molecular Dynamics Simulations Reveal a Rotationally Fluid Adsorption State of α-Pinene on Silica
A rotationally fluid state of α-pinene at fused silica/vapor interfaces is revealed by computational and experimental vibrational sum frequency generation (SFG) studies. We report the first assignment of the vibrational modes in the notoriously congested C-H stretching region of α-pinene and identify its bridge methylene group on the four-membered ring ("βCH2") as the origin of its dominant spectral feature. We find that the spectra are perfused with Fermi resonances that need to be accounted for explicitly in the computation of vibrational spectra of strained hydrocarbons such α-pinene. The preferred orientations of α-pinene are consistent with optimization of van der Waals contacts with the silica surface that results in a bimodal distribution of highly fluxional orientations in which the βCH2 group points "towards" or "away from” the surface. The reported findings are particularly relevant to the exposure of α-pinene to primary oxidants in heterogeneous catalytic pathways that exploit α-pinene as a sustainable feedstock for fine chemicals and polymers.
Competitive B2 and B33 Nucleation during Solidification of Ni 50 Zr 50 Alloy: Molecular Dynamics Simulation and Classical Nucleation Theory
We studied the homogenous nucleation of the stoichiometric B2 and B33 phases in the Ni 50 Zr 50 alloy using the persistent embryo method and the classical nucleation theory. The two phases become very close competitors at large supercoolings, which is consistent with the experimental observations. In the case of the B2 phase, the linear temperature dependence of the solid–liquid interface (SLI) free energy extrapolated to the melting temperature leads to the same value as the one obtained from the capillarity fluctuation method (CFM). In the case of the B33 phases, the SLI free energy is also a linear function of temperature at large supercoolings, but the extrapolation to the melting temperature leads to a value which is considerably different from the CFM value. This is persistent with the large anisotropy of the SLI properties of the B33 phase nearby the melting temperature observed in the simulation of the nominally flat interface migration.
Buckybomb: Reactive Molecular Dynamics Simulation
Not Available
Molecular Dynamics Simulations of Ion-Containing Polymers Using Generic Coarse-Grained Models
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Uncovering Local Correlations in Polymer Electrolytes by X-ray Scattering and Molecular Dynamics Simulations
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Molecular Dynamics Simulations of the Effects of Entanglement on Polymer Crystal Nucleation
Not provided.
Unique Phase Behavior of Inverse Tapered Block Copolymers: Self-Consistent Field Theory and Molecular Dynamics Simulations
Using theory and simulation, we study the microphase separated structures of inverse tapered block copolymers. These are AB block copolymers with a gradient region inserted between the pure A and B blocks that smoothly changes in composition from B to A, with the B-side of the taper bonded to the pure A block. Tapering is a means to increase miscibility between polymer blocks, and by controlling the length of the taper, the phase behavior and domain spacing can be adjusted. As opposed to better known ABAB tetrablock copolymers that also have four alternating A-rich and B-rich regions, here the intermediate region has a partially mixed composition, promoting relatively diblock-like behavior for shorter inverse tapers or low segregation strength but unique behavior as a function of increasing segregation strength for some systems. In particular, for systems in which 50% of the backbone is the taper, the larger of the two pure end blocks - composed of the overall majority component - can phase separate analogously to the minority component of a diblock copolymer, creating cylinder and network phases in which the majority component’s pure block is the minority phase in a matrix of a relatively disordered mixture of the tapered region and the minority component’s pure block.
Growth Mechanism and Kinetics of Diamond in Liquid Gallium from Quantum Mechanics Molecular Dynamics Simulations
Not provided.