The hydration of Li+ and Mg2+ in subnano carbon nanotubes using a multiscale theoretical approach

Ruirui Liu; Zhuanfang Jing; Yifan Shao; Yongquan Zhou; Fayan Zhu; Hongyan Liu

doi:10.3389/fchem.2023.1103792

The hydration of Li⁺ and Mg²⁺ in subnano carbon nanotubes using a multiscale theoretical approach

Front Chem. 2023 Feb 2:11:1103792. doi: 10.3389/fchem.2023.1103792. eCollection 2023.

Authors

Ruirui Liu^{1

2}, Zhuanfang Jing^{1

2}, Yifan Shao^{1

2}, Yongquan Zhou^{1

2}, Fayan Zhu^{1

2}, Hongyan Liu^{1

2}

Affiliations

¹ Key Laboratory of Comprehensive and Highly Efficient Utilization of Salt Lake Resources, Qinghai Institute of Salt Lakes, Chinese Academy of Sciences, Xining, Qinghai, China.
² Key Laboratory of Salt Lake Resources Chemistry of Qinghai Province, Qinghai Institute of Salt Lakes, Chinese Academy of Sciences, Xining, Qinghai, China.

Abstract

The separation of brines with high Mg/Li mass ratios is a huge challenge. To provide a theoretical basis for the design of separation materials, the hydration of Li⁺ and Mg²⁺ in confinement using carbon nanotubes (CNTs) as the 1-D nanopore model was investigated using a multiscale theoretical approach. According to the analysis of the first coordination layer of cations, we determined that the coordination shells of two cations exist inside CNTs, while the second coordination shells of the cations are unstable. Moreover, the results of the structure analysis indicate that the hydration layer of Li⁺ is not complete in CNTs with diameters of 0.73, 0.87, and 1.00 nm. However, this does not occur in the 0.60 nm CNT, which is explained by the formation of contact ion pairs (CIP) between Li⁺ and Cl^- that go through a unstable solvent-shared ion pair [Li(H₂O)₄]⁺, and this research was further extended by 400 ns in the 0.60 nm CNT to address the aforementioned results. However, the hydration layer of Mg²⁺ is complete and not sensitive to the diameter of CNTs using molecular dynamics simulation and an ab initio molecular dynamics (AIMD) method. Furthermore, the results of the orientation distribution of Li⁺ and Mg²⁺ indicate that the water molecules around Mg²⁺ are more ordered than water molecules around Li⁺ in the CNTs and are more analogous to the bulk solution. We conclude that it is energetically unfavorable to confine Li⁺ inside the 0.60-nm diameter CNT, while it is favorable for confining Li⁺ inside the other four CNTs and Mg²⁺ in all CNTs, which is driven by the strong electrostatic interaction between cations and Cl^-. In addition, the interaction between cations and water molecules in the five CNTs was also analyzed from the non-covalent interaction (NCI) perspective by AIMD.

Keywords: Li+ and Mg2+; carbon nanotube (CNT); hydration structure; molecular dynamics simulation; multiscale theoretical approach; separation.

Grants and funding

This work was financially supported by the National Natural Science Foundation (21973106) and the Nature Science Foundation of Qinghai Province (2022-ZJ-T03).