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Rechargeable aqueous zinc ion batteries (AZIBs) have gained considerable attention owing to their low cost and high safety, but dendrite growth, low plating/stripping efficiency, surface passivation, and self-erosion of the Zn metal anode are hindering their application. Herein, a one-step in situ molecular engineering strategy for the simultaneous construction of hierarchical MoS 2 double-layer nanotubes (MoS 2 -DLTs) with expanded layer-spacing, oxygen doping, structural defects, and an abundant 1T-phase is proposed, which are designed as an intercalation-type anode for "rocking-chair" AZIBs, avoiding the Zn anode issues and therefore displaying a long cycling life. Benefiting from the structural optimization and molecular engineering, the Zn 2+ diffusion efficiency and interface reaction kinetics of MoS 2 -DLTs are enhanced. When coupled with a homemade ZnMn 2 O 4 cathode, the assembled MoS 2 -DLTs//ZnMn 2 O 4 full battery exhibited impressive cycling stability with a capacity retention of 86.6% over 10 000 cycles under 1 A g -1 anode , outperforming most of the reported "rocking-chair" AZIBs. The Zn 2+ /H + cointercalation mechanism of MoS 2 -DLTs is investigated by synchrotron in situ powder X-ray diffraction and multiple ex situ characterizations. This research demonstrates the feasibility of MoS 2 for Zn-storage anodes that can be used to construct reliable aqueous full batteries.