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Ion-ion correlations across and between electrified graphene layers

机译:电镀石墨烯层的离子离子相关性

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When an ionic liquid adsorbs onto a porous electrode, its ionic arrangement is deeply modified due to a screening of the Coulombic interactions by the metallic surface and by the confinement imposed upon it by the electrode's morphology. In particular, ions of the same charge can approach at close contact, leading to the formation of a superionic state. The impact of an electrified surface placed between two liquid phases is much less understood. Here we simulate a full supercapacitor made of the 1-butyl-3-methylimidazolium hexafluorophosphate and nanoporous graphene electrodes, with varying distances between the graphene sheets. The electrodes are held at constant potential by allowing the carbon charges to fluctuate. Under strong confinement conditions, we show that ions of the same charge tend to adsorb in front of each other across the graphene plane. These correlations are allowed by the formation of a highly localized image charge on the carbon atoms between the ions. They are suppressed in larger pores, when the liquid adopts a bilayer structure between the graphene sheets. These effects are qualitatively similar to the recent templating effects which have been reported during the growth of nanocrystals on a graphene substrate. Published by AIP Publishing.
机译:当离子液体吸附到多孔电极上时,由于金属表面的库仑相互作用筛选和通过电极的形态施加在其上的限制,因此其离子排列深受修改。特别地,相同电荷的离子可以在紧密接触处接近,导致形成外阴状态。放置在两个液相之间的电镀表面的影响远不太清楚。在这里,我们模拟了由1-丁基-3-甲基咪唑鎓六氟磷酸钙和纳米多孔石墨烯电极制成的全部超级涂物,在石墨烯片之间的距离变化。通过允许碳电荷波动,电极保持恒定电位。在强大的监禁条件下,我们表明,相同电荷的离子倾向于在石墨烯平面上彼此的前面吸附。通过在离子之间的碳原子上形成高度局部图像电荷来允许这些相关性。当液体在石墨烯片之间采用双层结构时,它们被抑制在较大的孔中。这些效果与最近在石墨烯基材上的纳米晶体生长期间报道的最近的模板效果类似地类似。通过AIP发布发布。

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