Affiliation:
1. School of Chemical Engineering and Technology State Key Laboratory of Chemical Engineering Tianjin University Tianjin 300072 China
2. Zhejiang Institute of Tianjin University Shaoxing Zhejiang 312300 China
3. Haihe Laboratory of Sustainable Chemical Transformations Tianjin 300192 China
Abstract
AbstractVanadium‐based aqueous zinc‐ion batteries (AZIBs) exhibit significant potential for large‐scale energy storage applications, attributed to their inherent safety characteristics. Addressing the slow transport kinetics of divalent Zn2+ within the cathode lattice, thereby enhancing the rate capability and stability, is essential for the Zn‐V battery system. In this study, a local electric field (LEF) strategy is introduced to accelerate the Zn2+ diffusion by creating abundant oxygen vacancies (Ov) in V2O5. Comprehensive characterization and density functional theory (DFT) calculations reveal the formation of the Ov induced atomic‐level donor‐acceptor couple configuration, verify and visualize the LEF. The fabricated LEF‐enhanced vanadium oxide (LEF‐VO) exhibits exceptional rate capability, achieving 338.3 mA h g−1 at a current density of 10 A g−1, and maintaining 66.4% of its capacity over a range from 0.2 to 20 A g−1. Furthermore, the influence of the LEF on expediting Zn2+ diffusion kinetics is elucidated, correlating to the electrical force. This novel LEF approach offers valuable insights for advancing high‐rate cathode materials.
Funder
National Key Research and Development Program of China
Innovative Research Group Project of the National Natural Science Foundation of China