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      A nonmonotonic dependence of the contact angles on the surface polarity for a model solid surface

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          Abstract

          We found an unusual nonmonotonic contact angle dependence of the surface polarity (denoted as q) on a solid surface with specific charge patterns, where the contact angle firstly decreases and then increases as q increases from 0 e to 1.0 e.

          Abstract

          Based on molecular dynamics simulations, we found a nonmonotonic relationship between the contact angle of water droplets and the surface polarity on a solid surface with specific hexagonal charge patterns at room temperature. The contact angle firstly decreases and then increases as polarity (denoted as charge q) increases from 0 e to 1.0 e with a vertex value of q = 0.5 e. We observed a different wetting behavior for a water droplet on a conventional nonwetted solid surface when q ≤ 0.5 e, and a water droplet on an ordered water monolayer adsorbed on a highly polar solid surface when q > 0.5 e. The solid–water interaction, density of water, hydrogen bonds, and water structures were analyzed. Remarkably, there was up to six times difference in the solid–water interactions despite the same value of the apparent contact angle values.

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          Wetting: statics and dynamics

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            Is Open Access

            Canonical sampling through velocity-rescaling

            We present a new molecular dynamics algorithm for sampling the canonical distribution. In this approach the velocities of all the particles are rescaled by a properly chosen random factor. The algorithm is formally justified and it is shown that, in spite of its stochastic nature, a quantity can still be defined that remains constant during the evolution. In numerical applications this quantity can be used to measure the accuracy of the sampling. We illustrate the properties of this new method on Lennard-Jones and TIP4P water models in the solid and liquid phases. Its performance is excellent and largely independent on the thermostat parameter also with regard to the dynamic properties.
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              Wetting and spreading

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                Author and article information

                Journal
                PPCPFQ
                Physical Chemistry Chemical Physics
                Phys. Chem. Chem. Phys.
                Royal Society of Chemistry (RSC)
                1463-9076
                1463-9084
                2017
                2017
                : 19
                : 9
                : 6665-6670
                Affiliations
                [1 ]School of Physics
                [2 ]Shandong University
                [3 ]Jinan 250100
                [4 ]China
                [5 ]Division of Interfacial Water and Key Laboratory of Interfacial Physics and Technology
                [6 ]School of Electronic Engineering
                [7 ]Chengdu Technological University
                [8 ]Chengdu 611730
                [9 ]Shanghai Institute of Applied Physics
                [10 ]Chinese Academy of Sciences
                [11 ]Shanghai 201800
                [12 ]P. R. China
                Article
                10.1039/C6CP08275K
                556df162-ad79-4a23-b773-761c804fa5aa
                © 2017
                History
                Product
                Self URI (article page): http://xlink.rsc.org/?DOI=C6CP08275K

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