Dynamic transport of Zn2+ in ionic liquid intercalated V2O5 cathode for high-performance aqueous Zn-ion batteries

• We firstly reported the ionic liquids in the interlayers of V 2 O 5 cathode material for aqueous zinc ion batteries . • The ionic liquid between the V 2 O 5 layers optimized the interlayer charge distribution and widened the layer spacing. • We use in-situ spectroscopy to verify the dynamic response of ionic liquids during charging and discharging. • The intercalation of ionic liquids modifies the migration path of Zn 2+ , enlarging the channels and lowering the energy barrier. • 0.4[Bmim] + -V 2 O 5 || Zn of pouch full cells could stably cycled for 160 cycles at 50 mA g −1 , with an energy density of up to 310 W h kg −1 . Due to high safety and low-cost, aqueous Zn-ion batteries (ZIBs) are expected to be a promising next-generation energy storage technology. Exploiting high capacity and stable cathode materials are extremely important for the development of aqueous ZIBs. However, commercial V 2 O 5 despite its high theoretical specific capacity, suffers from structural instability during charging and discharging, and strong electrostatic forces seriously limit the diffusion of Zn 2+ . Herein, a novel dynamic transport mechanism of Zn 2+ is designed by intercalating organic cations (C 8 H 15 N 2 + ) from ionic liquids into the interlayers of V 2 O 5 . The electrostatic interaction between the C 8 H 15 N 2 + and the V-O layers enhance the structure stability of the layers and increase the interlayer spacing. Meanwhile, the C 8 H 15 N 2 + between the V-O layers reduce the diffusion energy barrier of Zn 2+ and enable the rapid dynamically transport of Zn 2+ . The diffusion coefficient is enhanced by an order of magnitude. The optimized V 2 O 5 cathode exhibits a high capacity of 268 mA h/g at 100 mA/g and excellent cycling stability (over 500 cycles at 200 mA/g with nearly 100 % coulombic efficiency). The home-made pouch cells deliver a high energy density of 310 W h kg −1 . This interesting idea opens up a new research direction for high-energy secondary batteries.

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Publication Details

Journal
Chemical Engineering Journal
Published
2024-12-25
DOI
https://doi.org/10.1016/j.cej.2024.158827
Citations
14
Primary Topic
Advanced battery technologies research
Type
article
Field-Weighted Citation Impact
2.92
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article

Dynamic transport of Zn2+ in ionic liquid intercalated V2O5 cathode for high-performance aqueous Zn-ion batteries

Xiaopeng Han, Wenbin Hu, Minjie Yao, Zanyu Chen et al.
14 citations
Chemical Engineering Journal
Advanced battery technologies research
2.92
article

Dynamic transport of Zn2+ in ionic liquid intercalated V2O5 cathode for high-performance aqueous Zn-ion batteries

Xiaopeng Han, Wenbin Hu, Minjie Yao, Zanyu Chen, Xingkai Wang, Wenzhe Su, Hui Sun, Yida Deng, Peng Cui, Hong Zhang
article en
14 citations

Abstract

• We firstly reported the ionic liquids in the interlayers of V 2 O 5 cathode material for aqueous zinc ion batteries . • The ionic liquid between the V 2 O 5 layers optimized the interlayer charge distribution and widened the layer spacing. • We use in-situ spectroscopy to verify the dynamic response of ionic liquids during charging and discharging. • The intercalation of ionic liquids modifies the migration path of Zn 2+ , enlarging the channels and lowering the energy barrier. • 0.4[Bmim] + -V 2 O 5 || Zn of pouch full cells could stably cycled for 160 cycles at 50 mA g −1 , with an energy density of up to 310 W h kg −1 . Due to high safety and low-cost, aqueous Zn-ion batteries (ZIBs) are expected to be a promising next-generation energy storage technology. Exploiting high capacity and stable cathode materials are extremely important for the development of aqueous ZIBs. However, commercial V 2 O 5 despite its high theoretical specific capacity, suffers from structural instability during charging and discharging, and strong electrostatic forces seriously limit the diffusion of Zn 2+ . Herein, a novel dynamic transport mechanism of Zn 2+ is designed by intercalating organic cations (C 8 H 15 N 2 + ) from ionic liquids into the interlayers of V 2 O 5 . The electrostatic interaction between the C 8 H 15 N 2 + and the V-O layers enhance the structure stability of the layers and increase the interlayer spacing. Meanwhile, the C 8 H 15 N 2 + between the V-O layers reduce the diffusion energy barrier of Zn 2+ and enable the rapid dynamically transport of Zn 2+ . The diffusion coefficient is enhanced by an order of magnitude. The optimized V 2 O 5 cathode exhibits a high capacity of 268 mA h/g at 100 mA/g and excellent cycling stability (over 500 cycles at 200 mA/g with nearly 100 % coulombic efficiency). The home-made pouch cells deliver a high energy density of 310 W h kg −1 . This interesting idea opens up a new research direction for high-energy secondary batteries.

Chemical Engineering JournalVol. 504
Tianjin University of Technology and Education (CN), Tianjin University (CN), Hainan University (CN), Ningxia University (CN), Fuzhou University (CN)
Affordable and clean energy
Openalex Percentile: Top 8%
Advanced battery technologies research
2.92
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