Issue 30, 2024

S@C composites constructed by a graded pore-making strategy for Mg–S batteries with outstanding rate performance

Abstract

Rechargeable magnesium batteries (RMBs) are low-cost energy storage devices, but they lack suitable cathode materials. Traditional sulfur (S8) cathodes have attracted much attention because of their high energy density; however, their cycling stability, conductivity, and reversibility are inferior. In this work, porous carbon materials with abundant pores were obtained by graded pore-making and S@C composite materials were obtained as cathodes for magnesium–sulfur batteries after loading porous carbon materials with sulfur. The interconnected pores provide the electrode material with a wealth of electrons and ion transport channels. The hollow structure of the carbon material facilitates the electrode–electrolyte contact area ensuring ion supply at high currents. Magnesium electricity assembled using S@C for the cathode had a high initial discharge specific capacity of 728 mA h g−1 at 50 mA g−1. When the magnification cycle reached 2000 mA g−1, it still had a high discharge-specific capacity of 242 mA h g−1, and the coulombic efficiency reached ∼100%, indicating excellent magnification performance. At a current density of 200 mA g−1, the maximum discharge-specific capacity was 420 mA h g−1. After 100 cycles, a discharge-specific capacity of ∼100 mA h g−1 remained with good cycling stability. This work provides a general strategy for the preparation of porous carbon composites and new insights for high-rate energy storage systems.

Graphical abstract: S@C composites constructed by a graded pore-making strategy for Mg–S batteries with outstanding rate performance

Supplementary files

Article information

Article type
Paper
Submitted
22 May 2024
Accepted
04 Jul 2024
First published
04 Jul 2024

New J. Chem., 2024,48, 13457-13465

S@C composites constructed by a graded pore-making strategy for Mg–S batteries with outstanding rate performance

P. Xue, P. Wang, X. Qin, Z. Wang, X. Jia and W. Wei, New J. Chem., 2024, 48, 13457 DOI: 10.1039/D4NJ02374A

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