| Literature DB >> 25806965 |
Yuesheng Wang1, Jue Liu2, Byungju Lee3, Ruimin Qiao4, Zhenzhong Yang1, Shuyin Xu1, Xiqian Yu2, Lin Gu1, Yong-Sheng Hu1, Wanli Yang4, Kisuk Kang3, Hong Li1, Xiao-Qing Yang2, Liquan Chen1, Xuejie Huang1.
Abstract
The aqueous sodium-ion battery system is a safe and low-cost solution for large-scale energy storage, because of the abundance of sodium and inexpensive aqueous electrolytes. Although several positive electrode materials, for example, Na₀.₄₄MnO₂, were proposed, few negative electrode materials, for example, activated carbon and NaTi₂(PO₄)₃, are available. Here we show that Ti-substituted Na₀.₄₄MnO₂ (Na₀.₄₄[Mn₁-xTix]O₂) with tunnel structure can be used as a negative electrode material for aqueous sodium-ion batteries. This material exhibits superior cyclability even without the special treatment of oxygen removal from the aqueous solution. Atomic-scale characterizations based on spherical aberration-corrected electron microscopy and ab initio calculations are utilized to accurately identify the Ti substitution sites and sodium storage mechanism. Ti substitution tunes the charge ordering property and reaction pathway, significantly smoothing the discharge/charge profiles and lowering the storage voltage. Both the fundamental understanding and practical demonstrations suggest that Na₀.₄₄[Mn₁-xTix]O₂ is a promising negative electrode material for aqueous sodium-ion batteries.Entities:
Year: 2015 PMID: 25806965 DOI: 10.1038/ncomms7401
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919