Operation of MXene-Derived Zinc-Preintercalated Bilayered Vanadium Oxide Cathode in Aqueous Zn-Ion Batteries
Article 2025 en
Authors
TA
Timofey Averianov
KM
Kyle Matthews
XZ
Xinle Zhang
Abstract
2 min read
Layered hydrated vanadium oxides, particularly those with bilayered structures, show remarkable electrochemical performance as cathodes for aqueous Zn-ion batteries (AZIBs). However, their wide-scale adoption is hindered by limited understanding of their charge storage mechanisms in different Zn-containing electrolytes. Here, we demonstrate the first synthesis of a MXene-derived Zn-preintercalated bilayered vanadium oxide (MD-ZVO) with a nanoflower-like morphology comprised of two-dimensional (2D) nanosheets, achieved via a two-step dissolution-recrystallization process. The strategic Zn<sup>2+</sup> preintercalation establishes well-defined ion diffusion pathways, while the nanoflower-like assembly of 2D nanosheets enhances structural integrity, together contributing to improved electrochemical performance over other layered vanadium oxides. A systematic evaluation of four electrolytes (2 M ZnSO<sub>4</sub>, 2.6 M Zn-(OTf)<sub>2</sub>, 2 M ZnCl<sub>2</sub>, and 30 m ZnCl<sub>2</sub>) showed that MD-ZVO electrodes delivered high reversible capacities (450 and 315 mAh g<sup>-1</sup> at 0.1 A g<sup>-1</sup>), excellent rate capability (223 mAh g<sup>-1</sup> for both electrolytes at 1.0 A g<sup>-1</sup>), and good electrochemical stability (84% and 48% over 1000 cycles at 1.0 A g<sup>-1</sup>) in saturated 2.6 M Zn-(OTf)<sub>2</sub> and highly concentrated 30 m ZnCl<sub>2</sub>, respectively. The material's superior electrochemical stability in concentrated electrolytes is attributed to suppressed vanadium oxide dissolution during cycling. <i>In situ</i> and <i>ex situ</i> XRD analyses of MD-ZVO electrodes reveal larger contribution of Zn<sup>2+</sup>-associated species for charge storage in cells containing 2.6 M Zn-(OTf)<sub>2</sub> and proton dominant charge transfer in cells containing 30 m ZnCl<sub>2</sub>. Additionally, the combination of <i>in situ</i> and <i>ex situ</i> characterization demonstrates the reversible formation of Zn <sub><i>x</i></sub> OTf <sub><i>y</i></sub> (OH)<sub>2<i>x</i>-<i>y</i></sub> ·<i>n</i>H<sub>2</sub>O in cells using 2.6 M Zn-(OTf)<sub>2</sub> and Zn<sub>5</sub>(OH)<sub>8</sub>Cl<sub>2</sub>·H<sub>2</sub>O in cells using 30 m ZnCl<sub>2</sub> on the MD-ZVO electrode surface over extended cycling. This work highlights the superior performance of nanoflower MD-ZVO for cathodes in aqueous Zn-ion batteries, which benefits from the proper selection of highly concentrated electrolytes that enable better utilization of the cathode material.
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