Vanadium-based materials, which offer multiple oxidation states and rich redox reactions in zinc-ion batteries (ZIBs), have gained substantial attention. However, achieving green and efficient preparation of vanadium oxides-based materials featured with a controlled content of different heterovalent vanadium remains a significant challenge. Herein, a vanadium-supramolecular flower-shaped material (VSF) with heterovalent vanadium was prepared using NH 4 VO 3 as vanadium metal center and hexamethylenetetramine as organic ligand in aqueous solution. The optimal ratio of material (PVSF) after controlling VSF presintering is 2/ 1 (V 5+ /V 4+ ). Employing PVSF-2/1 as cathode in ZIBs can achieve a high specific capacity of 398.9 mAh g −1 at 0.2 A g −1 , which is increased by 0.2 and 3.5 times as compared with that of pure VO 2 and V 2 O 5 , respectively. After 2000 cycles, it still delivers a specific capacity of 225 mAh g −1 at 5.0 A g −1 . The Zn∥PVSF-2/1 pouch cells were assembled with a satisfactory specific capacity of 339 mAh g −1 at a current of 0.2 A g −1 . The excellent performance is ascribed to regulation and coordinated promotion of heterovalent states. The structural pathways corresponding to V 5+ act as Zn 2+ transport channels to increase Zn 2+ transport capability. The V 4+ cause high charge density distribution of the V-O lattice layer to provide abundant active sites for the adsorption/desorption process of Zn 2+ .