Zinc‐Ion and Proton as Joint Charge Carriers of S‐MoO2 for High‐Capacity Aqueous Zinc‐Ion Batteries

Abstract Molybdenum‐based materials are regarded as promising candidates for aqueous zinc‐ion batteries (AZIBs) because of their multi‐valences and high specific capacity. However, the structural instability of MoS 2 and sluggish reaction kinetics of MoO 2 restrict their further development in AZIBs. Herein, the MoO 2 with in situ inherited sulfur atoms (S‐MoO 2 ) is successfully prepared by heat treatment of MoS 2 in static air. Benefiting from the synergistic effects of inherited S atoms and introduced O vacancies, the S‐MoO 2 exhibits higher specific/rate capacities (236 mAh g −1 at 0.1 A g −1 and 105 mAh g −1 at 5.0 A g −1 ) and better cycling stability (81% capacity retention after 2000 cycles at 2.0 A g −1 ) than the perfect MoO 2 . More significantly, the in situ electrochemical quartz crystal microbalance (EQCM) and ex situ spectroscopic techniques comprehensively elucidate that zinc‐ion and proton as joint charge carriers insert/extract into/from S‐MoO 2 through the (011) and (020) planes with high reversibility. This work provides a guideline for understanding the multi‐ion storage mechanism of cathode materials for high‐capacity AZIBs.