Hydrated cation–π interactions of π-electrons with hydrated Mg2+ and Ca2+ cations

水化能 化学 石墨烯 吸附 碱土金属 分子 无机化学 溶剂化壳 化学物理 碱金属 离子 物理化学 溶剂化 材料科学 纳米技术 有机化学
作者
Liuhua Mu,Guosheng Shi,Haiping Fang
出处
期刊:Journal of Chemical Physics [American Institute of Physics]
卷期号:160 (21) 被引量:1
标识
DOI:10.1063/5.0210995
摘要

Hydrated cation–π interactions at liquid–solid interfaces between hydrated cations and aromatic ring structures of carbon-based materials are pivotal in many material, biological, and chemical processes, and water serves as a crucial mediator in these interactions. However, a full understanding of the hydrated cation–π interactions between hydrated alkaline earth cations and aromatic ring structures, such as graphene remains elusive. Here, we present a molecular picture of hydrated cation–π interactions for Mg2+ and Ca2+ by using the density functional theory methods. Theoretical results show that the graphene sheet can distort the hydration shell of the hydrated Ca2+ to interact with Ca2+ directly, which is water–cation–π interactions. In contrast, the hydration shell of the hydrated Mg2+ is quite stable and the graphene sheet interacts with Mg2+ indirectly, mediated by water molecules, which is the cation–water–π interactions. These results lead to the anomalous order of adsorption energies for these alkaline earth cations, with hydrated Mg2+–π < hydrated Ca2+–π when the number of water molecules is large (n ≥ 6), contrary to the order observed for cation–π interactions in the absence of water molecules (n = 0). The behavior of hydrated alkaline earth cations adsorbed on a graphene surface is mainly attributed to the competition between the cation–π interactions and hydration effects. These findings provide valuable details of the structures and the adsorption energy of hydrated alkaline earth cations adsorbed onto the graphene surface.
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