Xin JinXianfen WangYalan LiuMinjun KimMin CaoHuanhuan XieShantang LiuXianbao WangWei HuangAshok Kumar NanjundanBrian YuliartoXingyun LiYusuke Yamauchi
Abstract Exploration of advanced carbon anode material is the key to circumventing the sluggish kinetics and poor rate capability for potassium ion storage. Herein, a synergistic synthetic strategy of engineering both surface and structure is adopted to design N, S co‐doped carbon nanotubes (NS‐CNTs). The as‐designed NS‐CNTs exhibit unique features of defective carbon surface, hollow tubular channel, and enlarged interlayer space. These features significantly contribute to a large potassium storage capacity of 307 mA h g −1 at 1 A g −1 and a remarkable rate performance with a capacity of 151 mA h g −1 even at 5 A g −1 . Furthermore, an excellent cyclability with 98% capacity retention after 500 cycles at 2 A g −1 is also achieved. Systematic analysis by in situ Raman spectroscopy and ex situ TEM demonstrates the structural stability and reversibility in the charge–discharge process. Although the kinetics studies reveal the capacitive‐dominated process for potassium storage, density functional theory calculations provide evidence that N, S co‐doping contributes to expanding the interlayer space to promote the K‐ion insertion, improving the electronic conductivity, and providing ample defective sites to favor the K‐ion adsorption.
Yongwen SunHao XiaoHaibo LiYezeng HeYa ZhangYi HuZhicheng JuQuanchao ZhuangYanhua Cui
Yun WangYalda Zamani KeteklahijaniRuishuai WangLiang LiuWenfeng JiangJia GuoDong YangUttandaraman SundararajMohammad ArjmandJian Liu
Sie-Young ChoiGuk‐Tae KimMoonsu KimGibaek Lee
Rui WuSiguo ChenJianghai DengXun HuangYujie SongRuiyi GanXiaoju WanZidong Wei
Zili XuMeiling FanJunjun WangFangfang ZhangWeiran LinHaining Zhang