阳极
电解质
化学工程
电化学
化学
钠
储能
材料科学
有机化学
电极
量子力学
物理
工程类
物理化学
功率(物理)
作者
Wufeng Fan,Yingxv Gao,Qunbo Hui,Zechao Ma,He Gan,Xiaohong Xia,Hongbo Liu
标识
DOI:10.1016/j.cej.2023.142963
摘要
The development of sodium-ion batteries has been seriously discouraged by the major limitation in the rate capability and the cycle life of the anode materials. Sn4P3 is recognized as a potential anode for sodium -ion batteries owing to its ultrahigh specific capacity and low cost, but the great volumetric change and low intrinsic electrical conductivity severely limit the cycling performance. Herein, we propose a closed-ended MXene and Sn4P3 hybrid consisting of active Sn4P3 porous hollow nanospheres (Sn4P3 HS) armored by a conductive MXene shell. Notably, the outer MXene shell protects Sn4P3 from direct exposure to the electrolyte and only allows the inward expansion of Sn4P3 into the hollow space, resulting in the formation of a thin solid-electrolyte interphase layer of high stability. As predicted, the hybrids can deliver an extraordinarily high capacity of 302.1 mAh g−1 even at an ultrahigh rate of 10 A g−1 and cycle at 1 A g−1 for 1500 cycles with a capacity retention of 94.9%. Moreover, the Sn4P3 HS@MXene//Na3V2(PO4)3/C full cell exhibits an outstanding energy density of 287.8 Wh kg−1 and good cyclic ability (390.5 mAh g−1 at 1A g−1 after 500 cycles), exhibiting a great potential in practical application.
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