An extended π-conjugated organosulfide-based cathode for highly reversible sodium metal batteries

被引:1
|
作者
Li, Xin [1 ]
Si, Yubing [1 ]
Tang, Shuai [1 ]
Fu, Yongzhu [1 ]
机构
[1] Zhengzhou Univ, Coll Chem, Zhengzhou 450001, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
ORGANIC ELECTRODE; CHALLENGES; ANODES; CHARGE;
D O I
10.1039/d3ta01055d
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Na-organic batteries are a promising candidate for grid-scale energy storage due to the abundance of Na and absence of transition metal elements. However, the shuttle effect of soluble redox-active organics induces low coulombic efficiency and fast capacity decay, especially collocated with the highly reactive Na metal anode. Herein, we uncover that 2,3,6,7,10,11-triphenylenehexathiol (THT) with the largest conjugated plane and 18 pi electrons has low binding energy with ether solvent. Therefore, THT has a low solubility of <0.02 g L-1 and thus the shuttle effect is evidently mitigated. Furthermore, the trace amounts of dissolved THT-based redox mediators can be well confined by the Nafion membrane due to the large molecular size and the Na-THT battery achieves a reversible capacity of ca. 190 mA h g(-1) with stable cycling over 700 times. Meanwhile, the energy density of the Na-THT battery with the thin-film Na metal anode remains at 113.8 W h kg(-1) at the 400(th) cycle. The work demonstrates the advantages and prospects of large conjugated organic cathodes in Na-organic batteries for large-scale energy storage.
引用
收藏
页码:8694 / 8699
页数:6
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