材料科学
钴
锂(药物)
离子
化学工程
纳米技术
无机化学
共价键
冶金
有机化学
化学
医学
工程类
内分泌学
作者
Changda Wang,Hui Xie,Shuangming Chen,Binghui Ge,Daobin Liu,Chuanqiang Wu,Wenjie Xu,Wangsheng Chu,Ganguli Babu,Pulickel M. Ajayan,Li Song
标识
DOI:10.1002/adma.201802525
摘要
Abstract With the unique‐layered structure, MXenes show potential as electrodes in energy‐storage devices including lithium‐ion (Li + ) capacitors and batteries. However, the low Li + ‐storage capacity hinders the application of MXenes in place of commercial carbon materials. Here, the vanadium carbide (V 2 C) MXene with engineered interlayer spacing for desirable storage capacity is demonstrated. The interlayer distance of pristine V 2 C MXene is controllably tuned to 0.735 nm resulting in improved Li‐ion capacity of 686.7 mA h g −1 at 0.1 A g −1 , the best MXene‐based Li + ‐storage capacity reported so far. Further, cobalt ions are stably intercalated into the interlayer of V 2 C MXene to form a new interlayer‐expanded structure via strong V–O–Co bonding. The intercalated V 2 C MXene electrodes not only exhibit superior capacity up to 1117.3 mA h g −1 at 0.1 A g −1 , but also deliver a significantly ultralong cycling stability over 15 000 cycles. These results clearly suggest that MXene materials with an engineered interlayer distance will be a rational route for realizing them as superstable and high‐performance Li + capacitor electrodes.
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