材料科学
相间
阴极
碳纤维
硫黄
化学工程
离子
氧化还原
硫化物
钠
电极
电导率
离子电导率
纳米技术
电解质
化学
有机化学
复合材料
物理化学
工程类
复合数
冶金
生物
遗传学
作者
Chuanfang Wu,Yaojie Lei,Laura Simonelli,Dino Tonti,Ashley P. Black,Xinxin Lü,Wei‐Hong Lai,Xiaolan Cai,Yunxiao Wang,Qinfen Gu,Shulei Chou,Hua‐Kun Liu,Guoxiu Wang,Shixue Dou
标识
DOI:10.1002/adma.202108363
摘要
Porous carbon has been widely used as an efficient host to encapsulate highly active molecular sulfur (S) in Li-S and Na-S batteries. However, for these sub-nanosized pores, it is a challenge to provide fully accessible sodium ions with unobstructed channels during cycling, particularly for high sulfur content. It is well recognized that solid interphase with full coverage over the designed architectures plays critical roles in promoting rapid charge transfer and stable conversion reactions in batteries, whereas constructing a high-ionic-conductivity solid interphase in the pores is very difficult. Herein, unique continuous carbonaceous pores are tailored, which can serve as multifunctional channels to encapsulate highly active S and provide fully accessible pathways for sodium ions. Solid sodium sulfide interphase layers are also realized in the channels, showing high Na-ion conductivity toward stabilizing the redox kinetics of the S cathode during charge/discharge processes. This systematically designed carbon-hosted sulfur cathode delivers superior cycling performance (420 mAh g-1 at 2 A g-1 after 2000 cycles), high capacity retention of ≈90% over 500 cycles at current density of 0.5 A g-1 , and outstanding rate capability (470 mAh g-1 at 5 A g-1 ) for room-temperature sodium-sulfur batteries.
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