摘要
Rechargeable magnesium batteries (RMBs) are regarded as one of the promising candidates of next generation of battery technologies, but seriously hampered by the sluggish kinetics of Mg 2+ -related cathode reactions. A pertinent solution is adding Li salt into the electrolyte to build a hybrid Mg/Li battery (MLB), which combines the high safety of Mg anode and the fast reaction kinetics of Li + with the cathode material . Herein, we propose a novel, simple, and cheap dual-salt electrolyte for MLBs, namely MgCl 2 –LiCl/THF, based on the exceptional synergetic effect between MgCl 2 and LiCl in THF . The 1.0 M electrolyte demonstrated desired ionic conductivity (1.3 mS cm –1 ), good compatibility with Mg anode, and adequate oxidation potential (2.2 V vs. Mg) for typical organic cathode materials including poly(anthraquinonyl sulfide) (PAQS), poly(1,4-anthraquinone) (P14AQ), and dilithium salt of poly(2,5-dihydroxy-p-benzoquinonyl sulfide) (Li 2 PDHBQS). Unlike PAQS and P14AQ adopting MgCl + as inserted cation, Li 2 PDHBQS selected Li + to participate in the reaction. Therefore it demonstrated superior electrochemical performance to most of previously reported inorganic and organic cathode materials for MLBs, including a high reversible capacity (282 mAh g −1 ), a high rate capability (72% @ 2000 mA g −1 ), and a high cycling stability (70% @ 500th cycle). The combination of MgCl 2 –LiCl/THF electrolyte and Li 2 PDHBQS cathode provides not only a successful example of high-performing and affordable MLBs, but also insights of ionic species in the electrolytes and their interactions with organic cathode materials, which are very significant for the further development of RMBs.
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