4.8 Article

Beyond conventional sodium-ion storage mechanisms: a combinational intercalation/conversion reaction mechanism in Ni-ion modified hydrated vanadate for high-rate sodium-ion storage

Journal

ENERGY STORAGE MATERIALS
Volume 47, Issue -, Pages 579-590

Publisher

ELSEVIER
DOI: 10.1016/j.ensm.2022.02.042

Keywords

Sodium-ion batteries; Anode materials; Intercalation/conversion reaction ; Rate capability; Charge storage capacity

Funding

  1. National Natural Science Foundation of China [NSFC 22108053, 91834301]
  2. Anhui Provincial Science and Technology Department Foundation [201903a05020021]
  3. Fundamental Research Funds for the Central Universities of China [JZ2021HGTA0175]

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The exploration of advanced anode materials is crucial for improving the performance of sodium-ion batteries. In this study, a new unconventional Na-ion storage mechanism was discovered in a modified hydrated vanadate material. This mechanism not only provides high capacity, but also demonstrates excellent cycling and rate performances. The findings have implications for enhancing the overall performance of sodium-ion batteries.
Exploration of advanced anode materials remains a great challenge in further promoting the performance of sodium-ion batteries. From the perspective of Na+ storage mechanisms, conversion/alloying-type anode materials typically offer high Na+ storage capacities, whereas the volume expansion during operation gives rise to unsatisfactory cycling stability. Intercalation-type anode materials with appropriate crystallographic structures have been identified to deliver decent cycling and rate performances. However, the deformations that the structures can withstand, as well as the limited numbers of available vacant sites in the crystal structures, significantly constrains the Na+ storage capacity. Herein, breaking from the conventional Na+ storage mechanisms, we reveal for the first time the combinational intercalation/conversion reaction mechanism upon Na+ storage in the Ni-ion modified hydrated vanadate (Ni0.24V2O5 & BULL;nH(2)O). Based on in-situ/ex-situ characterizations and theoretical analysis, the conversion reaction of the interlayer Ni3+ is found to be triggered after the Na+ intercalation process, which not only contributes to high specific capacities but also leads to fast and stable solid-state Na(+& nbsp;)diffusion. Paring Ni0.24V2O5 & BULL;nH(2)O with a Zn/Mg dual-doped P2-Na0.67MnO2 cathode material, a high-performance Na-ion battery prototype full cell is fabricated. The unconventional Na-ion storage mechanism that endows the anode material with both high capacity and outstanding cyclic and rate performances has implications for further boosting the comprehensive performance of sodium-ion batteries.

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