Published August 2023 | Version v1
Journal article

Unveiling the anionic redox chemistry in phosphate cathodes for sodium-ion batteries

  • 1. Beijing Advanced Innovation Center for Materials Genome Engineering, Institute for Advanced Materials and Technology, State Key Laboratory for Advanced Metals and Materials, University of Science and Technology Beijing, Beijing, 100083 (China)
  • 2. Tianjin Key Laboratory for Photoelectric Materials and Devices, School of Materials Science and Engineering, Tianjin University of Technology, Tianjin, 300384 (China)
  • 3. Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), Nankai University, Tianjin, 300071 (China)

Description

Anionic redox chemistry has aroused increasing attention in sodium-ion batteries (SIBs) by virtue of the appealing additional capacity. However, up to now, anionic redox reaction has not been reported in the mainstream phosphate cathodes for SIBs. Herein, the ultrathin VOPO4 nanosheets are fabricated as promising cathodes for SIBs, where the oxygen redox reaction is first activated accompanied by reversible ClO4 (from the electrolyte) insertion/extraction. As a result, the VOPO4 cathode harvests a record-high capacity (168 mAh g1 at 0.1 C) among its counterparts ever reported. Moreover, the ClO4 insertion efficiently expands the interlayer spacing of VOPO4 and accelerates the ion diffusion, enabling an unprecedentedly high rate performance (69 mAh g1 at 30 C). Via systematic ex situ characterizations and theoretical computations, the anionic redox chemistry and charge storage mechanism upon cycling are thoroughly elucidated. This study opens up a new avenue toward high-energy phosphate cathodes for SIBs by triggering anionic redox reactions. (© 2023 Wiley-VCH GmbH)

Availability note (English)

Available from: http://dx.doi.org/10.1002/adfm.202302200

Additional details

Identifiers

Publishing Information

Journal Title
Advanced Functional Materials (Internet)
Journal Volume
33
Journal Issue
33
Journal Page Range
p. 1-9
ISSN
1616-3028
CODEN
AFMDC6

Optional Information

Notes
AID: 2302200