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Ca$^{2+}$ pre-intercalated bilayered vanadium oxide for high-performance aqueous Mg-ion batteries
https://orcid.org/0000-0002-2507-5477
https://orcid.org/0000-0002-7828-183X
https://orcid.org/0000-0002-5134-7130
https://orcid.org/0000-0001-9295-2110
The “oxygen-rich” Ca$^{2+}$ pre-intercalated bilayered vanadium oxide (CaVOnH) was synthesized via hydrothermal method and determined as a monoclinic structure with reasonable lattice parameters. CaVOnH achieves a first discharge capacity of 273 mAh g$^{-1}$ with capacity retention of 91% at 50 mA g$^{-1}$ in 0.8 m Mg(TFSI)2–85%PEG-15%H$_2$O (polyethylene glycol, PEG), but limited rate capability due to the low ionic conductivity of electrolyte. Dimethyl sulfoxide (DMSO) is used as a co-solvent to tune the physical-chemical properties of aqueous Mg-ion electrolyte (AME), resulting in the reorganization of Mg$^{2+}$ solvation and hydrogen bond network. The AME containing DMSO shows improved ionic conductivity, low viscosity, and high Mg$^{2+}$ diffusion coefficient and allows CaVOnH and V$_2$O$_5$ to achieve a much-improved rate capability and capacity. Moreover, the reaction mechanism and reversibility of CaVOnH are elucidated by combining in operando and ex situ techniques. The results demonstrate that CaVOnH undergoes 2-phase reaction and solid solution, the variation of oxidation state and the local environment of vanadium, and reversible formation/decomposition of MgF$_2$ cathode electrolyte interface during Mg$^{2+}$ (de)intercalation, where MgF$_2$ originated from the decomposition of TFSI$^−$.
Ca$^{2+}$ pre-intercalated bilayered vanadium oxide for high-performance aqueous Mg-ion batteries
https://orcid.org/0000-0002-2507-5477
https://orcid.org/0000-0002-7828-183X
https://orcid.org/0000-0002-5134-7130
https://orcid.org/0000-0001-9295-2110
The “oxygen-rich” Ca$^{2+}$ pre-intercalated bilayered vanadium oxide (CaVOnH) was synthesized via hydrothermal method and determined as a monoclinic structure with reasonable lattice parameters. CaVOnH achieves a first discharge capacity of 273 mAh g$^{-1}$ with capacity retention of 91% at 50 mA g$^{-1}$ in 0.8 m Mg(TFSI)2–85%PEG-15%H$_2$O (polyethylene glycol, PEG), but limited rate capability due to the low ionic conductivity of electrolyte. Dimethyl sulfoxide (DMSO) is used as a co-solvent to tune the physical-chemical properties of aqueous Mg-ion electrolyte (AME), resulting in the reorganization of Mg$^{2+}$ solvation and hydrogen bond network. The AME containing DMSO shows improved ionic conductivity, low viscosity, and high Mg$^{2+}$ diffusion coefficient and allows CaVOnH and V$_2$O$_5$ to achieve a much-improved rate capability and capacity. Moreover, the reaction mechanism and reversibility of CaVOnH are elucidated by combining in operando and ex situ techniques. The results demonstrate that CaVOnH undergoes 2-phase reaction and solid solution, the variation of oxidation state and the local environment of vanadium, and reversible formation/decomposition of MgF$_2$ cathode electrolyte interface during Mg$^{2+}$ (de)intercalation, where MgF$_2$ originated from the decomposition of TFSI$^−$.
Ca$^{2+}$ pre-intercalated bilayered vanadium oxide for high-performance aqueous Mg-ion batteries
https://orcid.org/0000-0002-2507-5477
https://orcid.org/0000-0002-7828-183X
https://orcid.org/0000-0002-5134-7130
https://orcid.org/0000-0001-9295-2110
The “oxygen-rich” Ca$^{2+}$ pre-intercalated bilayered vanadium oxide (CaVOnH) was synthesized via hydrothermal method and determined as a monoclinic structure with reasonable lattice parameters. CaVOnH achieves a first discharge capacity of 273 mAh g$^{-1}$ with capacity retention of 91% at 50 mA g$^{-1}$ in 0.8 m Mg(TFSI)2–85%PEG-15%H$_2$O (polyethylene glycol, PEG), but limited rate capability due to the low ionic conductivity of electrolyte. Dimethyl sulfoxide (DMSO) is used as a co-solvent to tune the physical-chemical properties of aqueous Mg-ion electrolyte (AME), resulting in the reorganization of Mg$^{2+}$ solvation and hydrogen bond network. The AME containing DMSO shows improved ionic conductivity, low viscosity, and high Mg$^{2+}$ diffusion coefficient and allows CaVOnH and V$_2$O$_5$ to achieve a much-improved rate capability and capacity. Moreover, the reaction mechanism and reversibility of CaVOnH are elucidated by combining in operando and ex situ techniques. The results demonstrate that CaVOnH undergoes 2-phase reaction and solid solution, the variation of oxidation state and the local environment of vanadium, and reversible formation/decomposition of MgF$_2$ cathode electrolyte interface during Mg$^{2+}$ (de)intercalation, where MgF$_2$ originated from the decomposition of TFSI$^−$.
Ca$^{2+}$ pre-intercalated bilayered vanadium oxide for high-performance aqueous Mg-ion batteries
Fu, Qiang (author, ) / Wu, Xiaoyu (author) / Luo, Xianlin (author) / Ding, Ziming (author) / Indris, Sylvio (author) / Sarapulova, Angelina (author) / Meng, Zhen (author) / Desmau, Morgane (author) / Wang, Zhengqi (author) / Hua, Weibo (author)
2024-01-01
103212 pages
Energy storage materials 66, 103212 (2024). doi:10.1016/j.ensm.2024.103212
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Electronic Resource
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