4.8 Article

VS4 anchored on Ti3C2 MXene as a high-performance cathode material for magnesium ion battery

期刊

JOURNAL OF POWER SOURCES
卷 518, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.jpowsour.2021.230731

关键词

Magnesium battery; Cathode; Ti3C2; VS4

资金

  1. National Natural Science Foundation of China [51801100, 51771092, 21975125, 51801099]
  2. Natural Science Foundation of the Jiangsu Higher Education Institutions of China [18KJB430014]
  3. Postgraduate Research & Practice Innovation Program of Jiangsu Province [SJCX18_0341]
  4. Six Talent Peaks Project in Jiangsu Province [XNY-020]
  5. Priority Academic Program Development (PAPD) of Jiangsu Higher Education Institutions

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Rechargeable magnesium batteries face challenges due to strong coulombic effects, but this study presents a high-performance system using hierarchical nano-micro hybrids to improve accessibility and reduce charge transfer resistance, achieving high discharge capacity, outstanding rate performance, and excellent cycling performance.
Rechargeable magnesium batteries (rMBs) are promising techniques suitable for large-scale energy storage systems with low-cost and high safety. However, their development is severely hindered by strong coulombic effect between bivalent Mg2+ and cathode materials. In this work, two dimensional hierarchical nano-micro hybrids are synthesized by in-situ generating VS4 nanosheets on carbon-coated Ti3C2 MXene matrix (denoted as VS4@Ti3C2/C). A high-performance rMB system is built by using the hierarchical nano-micro hybrids cathode, magnesium foil anode, and 0.25 M methylpyrrolidinium chloride in 0.25 M 2PhMgCl-AlCl3/tetrahydrofuran as the electrolyte. The existence of V-C bond proves that VS4 is anchored on the surface of Ti3C2 via a strong chemical bond, rather than simply by adsorption. The unique hierarchical nano-micro structure improves the accessibility of the electrolyte and reduces the charge transfer resistance, leading to a high discharge capacity of 492 mA h g-1 at 50 mA g-1, an outstanding rate performance of 129 mA h g-1 at 1000 mA g-1, and excellent cycling performance (over 900 cycles at 500 mA g-1). Moreover, reversible intercalation of MgCl + into VS4@Ti3C2/C is revealed by investigating the evolution of the hybrids during different electrochemical states. This study will shed light on designing high-performance MXene-based cathode materials for multivalent batteries.

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