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      Heterogeneous ice nucleation correlates with bulk-like interfacial water

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          Abstract

          Bulk-like interfacial water, a sub-ensemble of interfacial water, can be a predictor for heterogeneous ice nucleation.

          Abstract

          Establishing a direct correlation between interfacial water and heterogeneous ice nucleation (HIN) is essential for understanding the mechanism of ice nucleation. Here, we study the HIN efficiency on polyvinyl alcohol (PVA) surfaces with different densities of hydroxyl groups. We find that the HIN efficiency increases with the decreasing hydroxyl group density. By explicitly considering that interfacial water molecules of PVA films consist of “tightly bound water,” “bound water,” and “bulk-like water,” we reveal that bulk-like water can be correlated directly to the HIN efficiency of surfaces. As the density of hydroxyl groups decreases, bulk-like water molecules can rearrange themselves with a reduced energy barrier into ice due to the diminishing constraint by the hydroxyl groups on the PVA surface. Our study not only provides a new strategy for experimentally controlling the HIN efficiency but also gives another perspective in understanding the mechanism of ice nucleation.

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          Design of anti-icing surfaces: smooth, textured or slippery?

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            Crystal Nucleation in Liquids: Open Questions and Future Challenges in Molecular Dynamics Simulations

            The nucleation of crystals in liquids is one of nature's most ubiquitous phenomena, playing an important role in areas such as climate change and the production of drugs. As the early stages of nucleation involve exceedingly small time and length scales, atomistic computer simulations can provide unique insight into the microscopic aspects of crystallization. In this review, we take stock of the numerous molecular dynamics simulations that in the last few decades have unraveled crucial aspects of crystal nucleation in liquids. We put into context the theoretical framework of classical nucleation theory and the state of the art computational methods, by reviewing simulations of e.g. ice nucleation or crystallization of molecules in solutions. We shall see that molecular dynamics simulations have provided key insight into diverse nucleation scenarios, ranging from colloidal particles to natural gas hydrates, and that in doing so the general applicability of classical nucleation theory has been repeatedly called into question. We have attempted to identify the most pressing open questions in the field. We believe that by improving (i.) existing interatomic potentials; and (ii.) currently available enhanced sampling methods, the community can move towards accurate investigations of realistic systems of practical interest, thus bringing simulations a step closer to experiments.
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              A marine biogenic source of atmospheric ice-nucleating particles.

              The amount of ice present in clouds can affect cloud lifetime, precipitation and radiative properties. The formation of ice in clouds is facilitated by the presence of airborne ice-nucleating particles. Sea spray is one of the major global sources of atmospheric particles, but it is unclear to what extent these particles are capable of nucleating ice. Sea-spray aerosol contains large amounts of organic material that is ejected into the atmosphere during bubble bursting at the organically enriched sea-air interface or sea surface microlayer. Here we show that organic material in the sea surface microlayer nucleates ice under conditions relevant for mixed-phase cloud and high-altitude ice cloud formation. The ice-nucleating material is probably biogenic and less than approximately 0.2 micrometres in size. We find that exudates separated from cells of the marine diatom Thalassiosira pseudonana nucleate ice, and propose that organic material associated with phytoplankton cell exudates is a likely candidate for the observed ice-nucleating ability of the microlayer samples. Global model simulations of marine organic aerosol, in combination with our measurements, suggest that marine organic material may be an important source of ice-nucleating particles in remote marine environments such as the Southern Ocean, North Pacific Ocean and North Atlantic Ocean.
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                Author and article information

                Journal
                Sci Adv
                Sci Adv
                SciAdv
                advances
                Science Advances
                American Association for the Advancement of Science
                2375-2548
                April 2019
                12 April 2019
                : 5
                : 4
                : eaat9825
                Affiliations
                [1 ]Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
                [2 ]School of Mathematical, Physical and Computational Sciences, University of Reading, Whiteknights, Reading RG6 6AX, UK.
                [3 ]Physics Department and Shanghai Key Laboratory of Magnetic Resonance, East China Normal University, North Zhongshan Road 3663, Shanghai 200062, China.
                Author notes
                [* ]Corresponding author. Email: wangj220@ 123456iccas.ac.cn (J.W.); hezy@ 123456iccas.ac.cn (Z.H.)
                Author information
                http://orcid.org/0000-0003-4587-8979
                http://orcid.org/0000-0001-7942-8605
                http://orcid.org/0000-0002-6274-2048
                http://orcid.org/0000-0002-7478-4923
                Article
                aat9825
                10.1126/sciadv.aat9825
                6461451
                30993196
                f738bbcd-41de-4842-9fa7-be3a259b2eae
                Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC).

                This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license, which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.

                History
                : 24 April 2018
                : 14 February 2019
                Funding
                Funded by: Strategic Priority Research Program of the Chinese Academy of Sciences;
                Award ID: XDA09020000
                Funded by: Chinese National Nature Science Foundation;
                Award ID: 21733010
                Funded by: Chinese National Nature Science Foundation;
                Award ID: 51436004
                Funded by: Chinese National Nature Science Foundation;
                Award ID: 21503240
                Categories
                Research Article
                Research Articles
                SciAdv r-articles
                Applied Physics
                Surface Chemistry
                Chemistry
                Custom metadata
                Eunice Diego

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