Revealing an Interconnected Interfacial Layer in Solid-State Polymer Sodium Batteries

Journal Article (2019)
Author(s)

Chenglong Zhao (Chinese Academy of Sciences)

Lilu Liu (Chinese Academy of Sciences)

Yaxiang Lu (Chinese Academy of Sciences)

Marnix Wagemaker (TU Delft - RST/Storage of Electrochemical Energy)

Liquan Chen (Chinese Academy of Sciences)

Yong Sheng Hu (Chinese Academy of Sciences, Yangtze River Delta Physics Research Center, Liyang)

Research Group
RST/Storage of Electrochemical Energy
Copyright
© 2019 Chenglong Zhao, Lilu Liu, Yaxiang Lu, M. Wagemaker, Liquan Chen, Yong Sheng Hu
DOI related publication
https://doi.org/10.1002/anie.201909877
More Info
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Publication Year
2019
Language
English
Copyright
© 2019 Chenglong Zhao, Lilu Liu, Yaxiang Lu, M. Wagemaker, Liquan Chen, Yong Sheng Hu
Research Group
RST/Storage of Electrochemical Energy
Issue number
47
Volume number
58
Pages (from-to)
17026-17032
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Abstract

Replacing the commonly used nonaqueous liquid electrolytes in rechargeable sodium batteries with polymer solid electrolytes is expected to provide new opportunities to develop safer batteries with higher energy densities. However, this poses challenges related to the interface between the Na-metal anode and polymer electrolytes. Driven by systematically investigating the interface properties, an improved interface is established between a composite Na/C metal anode and electrolyte. The observed chemical bonding between carbon matrix of anode with solid polymer electrolyte, prevents delamination, and leads to more homogeneous plating and stripping, which reduces/suppresses dendrite formation. Full solid-state polymer Na-metal batteries, using a high mass loaded Na3V2(PO4)3 cathode, exhibit ultrahigh capacity retention of more than 92 % after 2 000 cycles and over 80 % after 5 000 cycles, as well as the outstanding rate capability.

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