<p>Aqueous zinc-ion batteries (AZIBs) have emerged as one of the most promising options for contemporary energy storage systems owing to their inherent low cost, high safety, and environmental friendliness. However, developing high-performance AZIB cathode materials that meet the requirements for large-scale applications remains a considerable challenge. This study employed a straightforward hydrothermal method to efficiently synthesize Y<sup>3+</sup> preintercalated hydrated vanadium oxide cathode material (VOH-Y). By introducing rare-earth Y<sup>3+</sup> ions into layered V<sub>10</sub>O<sub>24</sub>·nH<sub>2</sub>O, the original interlayer spacing was modulated; concurrently, this promoted the formation of a uniform two-dimensional nanosheet structure in VOH-Y, effectively optimizing the Zn<sup>2+</sup> diffusion path and the distribution of insertion/extraction active sites, thereby enhancing diffusion kinetics. Therefore, the VOH-Y cathode delivered a specific capacity of 374.99 mAh g<sup>−1</sup> at 0.5 A g<sup>−1</sup> with 90.18% capacity retention after 200 cycles. This work highlights the importance of the Y<sup>3+</sup> preintercalation strategy and provides new insights for developing high-performance AZIB cathode materials.</p>

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Y3+-Induced 2D Nano Vanadium Oxide Materials for High-Performance Aqueous Zinc Ion Batteries

  • Luyao Sun,
  • Ziyin Lu,
  • Shenglin Zhong,
  • Fangan Liang,
  • Lijie Song,
  • Yunjie Wang,
  • Rong Zheng,
  • Xiuxin Zheng,
  • Zhengguang Zou

摘要

Aqueous zinc-ion batteries (AZIBs) have emerged as one of the most promising options for contemporary energy storage systems owing to their inherent low cost, high safety, and environmental friendliness. However, developing high-performance AZIB cathode materials that meet the requirements for large-scale applications remains a considerable challenge. This study employed a straightforward hydrothermal method to efficiently synthesize Y3+ preintercalated hydrated vanadium oxide cathode material (VOH-Y). By introducing rare-earth Y3+ ions into layered V10O24·nH2O, the original interlayer spacing was modulated; concurrently, this promoted the formation of a uniform two-dimensional nanosheet structure in VOH-Y, effectively optimizing the Zn2+ diffusion path and the distribution of insertion/extraction active sites, thereby enhancing diffusion kinetics. Therefore, the VOH-Y cathode delivered a specific capacity of 374.99 mAh g−1 at 0.5 A g−1 with 90.18% capacity retention after 200 cycles. This work highlights the importance of the Y3+ preintercalation strategy and provides new insights for developing high-performance AZIB cathode materials.