Hierarchical assembly and superior sodium storage properties of a sea-sponge structured C/SnS@C nanocomposite

被引:33
作者
Chen, Shipei [1 ]
Xing, Ke [1 ]
Wen, Jiahao [2 ]
Wen, Ming [1 ]
Wu, Qingsheng [1 ]
Cui, Yi [3 ]
机构
[1] Tongji Univ, Shanghai Key Lab Chem Assessment & Sustainabil, Sch Chem Sci & Engn, Shanghai 200092, Peoples R China
[2] Chongqing Univ, Sch Elect Engn, Chongqing 400044, Peoples R China
[3] Stanford Univ, Dept Mat Sci & Engn, Stanford, CA 94305 USA
基金
中国国家自然科学基金;
关键词
GRAPHENE OXIDE COMPOSITE; HIGH-PERFORMANCE ANODE; HIGH-CAPACITY; LITHIUM STORAGE; POROUS CARBON; ION BATTERIES; GRAPHITE OXIDE; HIGH-STABILITY; HOLLOW CARBON; NANOPARTICLES;
D O I
10.1039/c8ta00833g
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
The exploration of electrode materials with superior rate capability and cyclability has been a critical challenge for sodium-ion batteries (SIBs). Herein, a new sea-sponge structured C/SnS@C nanocomposite has been fabricated through the hierarchical assembly of SnS2 nanoflakes on sea-sponge-like macrochannel-interconnected carbon spheres (S-MCSs) and subsequent carbon coating together with the phase transformation of SnS. A notably enhanced performance is achieved which is attributed to the formation of the sea-sponge-like rigid structure and layered SnS nanoflakes, which facilitate Na+ diffusion at a large current density based on the conductive S-MCS skeleton and carbon coating, thus significantly improving the kinetic process of Na+ insertion/extraction. When applied as an anode material for SIBs, the designed C/SnS@C composite exhibits superior cycling stability. It can endure a current density of 10 A g(-1) to complete the charge process in 22 s and deliver a capacity of 370 mA h g(-1) at 1 A g(-1) after five initial activation processes, with over 84% capacity retention from the 200(th) to the 2000(th) cycle, which is equivalent to 0.009% decay per cycle.
引用
收藏
页码:7631 / 7638
页数:8
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