Synergistic Cathode Design for High-Performance Dual-Salt Magnesium/Lithium-Ion Batteries Using 2D/2D 1T/2H-MoS2@Ti3C2Tx MXene Nanocomposite.

Magnesium-ion batteries (MIBs) and dual-salt magnesium/lithium-ion batteries (MLIBs) have emerged as promising contenders for next-generation energy storage. In contrast to lithium metal anode in lithium metal batteries, magnesium metal anode in MIBs and MLIBs presents a safer alternative due to the limited dendrite growth and higher volumetric capacity, along with higher natural abundance. This study explores a MLIB configuration with a novel cathode design by employing a 2D/2D nanocomposite of 1T/2H mixed phase MoS2 and delaminated Ti3C2Tx MXene (1T/2H-MoS2@MXene) to address challenges associated with slow kinetics of magnesium ions during cathode interactions. This cathode design takes advantage of the high electrical conductivity of Ti3C2Tx MXene and the expanded interlayer spacing with enhanced conductivity of the 1T metallic phase in 1T/2H mixed phase MoS2. Through a designed synthesis method, the resulting nanocomposite cathode maintains structural integrity, enabling the stable and reversible storage of dual Mg2+ and Li+ ions. The nanocomposite cathode demonstrates superior performance in MLIBs compared to individual components (253 mAh g-1 at 50 mA g-1, and 36% of capacity retention at 1,000 mA g-1), showcasing short ion transport paths and fast ion storage kinetics. This work represents a significant advancement in cathode material design for cost-effective and safe MLIBs.

Pillar-Structured Ti3 C2 Tx MXene with Engineered Interlayer Spacing for High-Performance Magnesium Batteries.

Two-dimentional (2D) Ti3 C2 Tx MXene has attracted significant attention in non-lithium-ion batteries due to its excellent electrical conductivity, high volumetric capacity, and ability to accommodate intercalants. Rechargeable magnesium batteries with Mg metal anodes are noted for their high theoretical energy density, potential safety, earth abundance, dendrite-free Mg2+ plating/stripping mechanism on the anode side, and low cost. Nevertheless, owing to the large polarity of divalent Mg2+ ions, the insertion of Mg2+ into the MXene layers suffers from sluggish kinetics, limiting the performance for storage of Mg2+ ions. Herein, a simple self-assembly strategy is demonstrated to achieve high magnesium ion storage capability with pillar-structured Ti3 C2 Tx MXene by intercalating a hyperbranched polyethylene ionomer containing quaternary ammonium ions. The ionomer intercalation/modification leads to the expansion of interlayer spacing of the MXene and, meanwhile, improves its affinity to low-polarity THF-based electrolyte. The delaminated ionomer-modified MXene shows significantly improved electrochemical performance as a cathode material for Mg batteries. It shows a promising cycling stability with a capacity retention of 86% after 400 cycles at 200 mA g-1 , as well as outstanding high-rate performance with a capacity of 110 mAh g-1 retained at 1,000 mA g-1 relative to 213 mAh g-1 at 20 mA g-1 .