Abstract

Aqueous sodium-ion batteries are practically promising for large-scale energy storage, however energy density and lifespan are limited by water decomposition. Current methods to boost water stability include, expensive fluorine-containing salts to create a solid electrolyte interface and addition of potentially-flammable co-solvents to the electrolyte to reduce water activity. However, these methods significantly increase costs and safety risks. Shifting electrolytes from near neutrality to alkalinity can suppress hydrogen evolution while also initiating oxygen evolution and cathode dissolution. Here, we present an alkaline-type aqueous sodium-ion batteries with Mn-based Prussian blue analogue cathode that exhibits a lifespan of 13,000 cycles at 10 C and high energy density of 88.9 Wh kg−1 at 0.5 C. This is achieved by building a nickel/carbon layer to induce a H3O+-rich local environment near the cathode surface, thereby suppressing oxygen evolution. Concurrently Ni atoms are in-situ embedded into the cathode to boost the durability of batteries.

Aqueous sodium-ion batteries show promise for large-scale energy storage, yet face challenges due to water decomposition, limiting their energy density and lifespan. Here, the authors report a cathode surface coating strategy in an alkaline electrolyte to enhance the stability of both electrolyte and battery.

Details

Title
Alkaline-based aqueous sodium-ion batteries for large-scale energy storage
Author
Wu, Han 1 ; Hao, Junnan 1 ; Jiang, Yunling 1 ; Jiao, Yiran 1 ; Liu, Jiahao 1 ; Xu, Xin 1 ; Davey, Kenneth 1   VIAFID ORCID Logo  ; Wang, Chunsheng 2   VIAFID ORCID Logo  ; Qiao, Shi-Zhang 1   VIAFID ORCID Logo 

 The University of Adelaide, School of Chemical Engineering, Adelaide, Australia (GRID:grid.1010.0) (ISNI:0000 0004 1936 7304) 
 University of Maryland, Department of Chemical and Biomolecular Engineering, College Park, USA (GRID:grid.164295.d) (ISNI:0000 0001 0941 7177) 
Pages
575
Publication year
2024
Publication date
2024
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2915815642
Copyright
© The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.