4.6 Article

Metal-Ions Intercalation Mechanism in Layered Anode From First-Principles Calculation

期刊

FRONTIERS IN CHEMISTRY
卷 9, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fchem.2021.677620

关键词

layer structure; first-principles; metal-ions battery; structural evolution; MoS2

资金

  1. National Natural Science Foundation of China [11902144]
  2. Natural Science Foundation of the Jiangsu Higher Education Institutions of China [19KJB430022]
  3. Postgraduate Research & Practice Innovation Program of Jiangsu Province [KYCX20_1074]

向作者/读者索取更多资源

The study shows that MoS2 has good electrochemical performance in lithium and sodium-ion batteries due to low ion migration energy barrier and high storage capability; however, it exhibits poor performance in magnesium and zinc-ion batteries, especially in zinc-ion batteries. The phase transformation of MoS2 from 2H to 1T during lithium and sodium ion intercalation leads to strong interaction between the ions and the anode, resulting in higher electrochemical performance, which is difficult to achieve in magnesium and zinc-ion batteries.
Layered structure (MoS2) has the potential use as an anode in metal-ions (M-ions) batteries. Here, first-principles calculations are used to systematically investigate the diffusion mechanisms and structural changes of MoS2 as anode in lithium (Li)-, sodium (Na)-, magnesium (Mg)- and Zinc (Zn)-ions batteries. Li and Na ions are shown to be stored in the MoS2 anode material due to the strong adsorption energies (similar to-2.25 eV), in contrast to a relatively weak adsorption of Mg and Zn ions for the pristine MoS2. To rationalize the results, we evaluate the charge transfer from the M-ions to the MoS2 anode, and find a significant hybridization between the adsorbed atoms and S atoms in the MoS2 anode. Furthermore, the migration energy barriers of M ions are explored using first-principles with the climbing image nudged elastic band (CINEB) method, and the migration energy barrier is in the order of Zn > Mg > Li > Na ions. Our results combined with the electrochemical performance experiments show that Li- and Na-ions batteries have good cycle and rate performance due to low ions migration energy barrier and high storage capability. However, the MoS2 anode shows poor electrochemical performance in Zn- and Mg-ions batteries, especially Zn-ion batteries. Further analysis reveals that the MoS2 structure undergoes the phase transformation from 2H to 1T during the intercalation of Li and Na ions, leading to strong interaction between M ions and the anode, and thus higher electrochemical performance, which, however, is difficult to occur in Mg- and Zn-ions batteries. This work focuses on the theoretical aspects of M-ions intercalation, and our findings may stimulate the experimental work for the intercalation of multi-ions to maximize the capacity of anode in M-ions batteries.

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