1T‐2H Mixed‐Phase MoS<sub>2</sub> Stabilized with a Hyperbranched Polyethylene Ionomer for Mg<sup>2+</sup>/Li<sup>+</sup> Co‐Intercalation Toward High‐Capacity Dual‐Salt Batteries
Jalal Rahmatinejad, Bahareh Raisi, Xudong Liu, Ximeng Zhang, Ahmad Sadeghi Chevinli, Liuqing Yang, Zhibin Ye
Abstract
Abstract Dual‐salt magnesium/lithium‐ion batteries (MLIBs) benefit from fast lithium ion diffusion on the cathode side while providing safety due to the dendrite‐free Mg 2+ stripping/plating mechanism on the anode side. Bulk MoS 2 (B‐MoS 2 ), as a cathode for magnesium‐ion batteries (MIBs), suffers from low conductivity and relatively van der Waals gaps and, consequently, resists against divalent Mg 2+ insertion due to the high Coulombic interactions. In MLIBs, it exhibits a Daniell‐cell type mechanism with the sole accommodation of Li + . In this paper, the synthesis of a 1T/2H mixed‐phase MoS 2 (MP‐MoS 2 ) modified with a hyperbranched polyethylene ionomer, I@MP‐MoS 2 , for high‐capacity MLIBs with a distinct Mg 2+ /Li + co‐intercalation mechanism is reported. Benefiting from the enhanced conductivity (due to 53% metallic 1T phase), expanded van der Waals gaps (79% expansion compared to B‐MoS 2 , 1.11 vs 0.62 nm), and enhanced interactions with THF‐based electrolytes following the modification, I@MP‐MoS 2 shows a dramatically increased Mg 2+ storage compared to its parent analogue (144 mAh g −1 vs ≈2 mAh g −1 at 20 mA g −1 ). In MLIBs, I@MP‐MoS 2 is demonstrated to exhibit remarkable specific capacities up to ≈270 mAh g −1 at 20 mA g −1 through a Mg 2+ /Li + co‐intercalation mechanism with 87% of capacity retention over 200 cycles at 100 mA g −1 .