阳极
锂(药物)
碳纳米管
兴奋剂
材料科学
纳米管
氮气
纳米技术
电化学
储能
碳纤维
化学工程
电极
化学
光电子学
复合材料
复合数
物理
工程类
内分泌学
物理化学
功率(物理)
有机化学
医学
量子力学
作者
Tian Liang,Huanwen Wang,Rui Wang,Beibei He,Yansheng Gong,Chunjie Yan
标识
DOI:10.1016/j.electacta.2021.138686
摘要
• Natural hematite is employed as the raw material to synthesize FeSe 2 @N-CNT. • This synthesis method is readily available and highly scalable. • 2. The FeSe 2 @N-CNT anode shows ultrafast rate capability to 20 A g −1 . • 3. Long-term cycle stability (953 mAh g −1 after 1500 cycles at 10 A g −1 ) is achieved. Fast−charging and high−capacity have become indispensable requirements for next−generation energy storage systems. However, large−scale fabrication of high−capacity anode materials for fast Li + storage remains a huge challenge. Herein, natural hematite is employed as the starting material to achieve scalable synthesis of nitrogen−doped carbon nanotube−buffered FeSe 2 (FeSe 2 @N−CNT) through a facile catalyzing & selenizing process. The readily−available raw materials and simple processing procedures are suitable to industrial−level batch production. In this FeSe 2 @N−CNT composite, the FeSe 2 particles are efficiently encapsulated into the interwoven carbon nanotube network, which can enlarge the contact area with electrolyte, enhance the electrical conductivity, shorten the Li + /e – diffusion length and buffer the drastic volume variation of FeSe 2 during lithiation/delithiation. As an anode material of lithium ion batteries (LIBs), the FeSe 2 @N−CNT electrode delivers a significantly high specific capacity of 806 mAh g −1 at a high current density of 20 A g −1 (relative to 915 mAh g −1 at 0.1 A g −1 ). More importantly, long−term cycle stability (953 mAh g −1 after 1500 cycles at 10 A g −1 ) is achieved, which outperforms most FeSe 2 −based Li + storage anodes reported so far. The easy−to−implement mass production and the high Li + storage property enable FeSe 2 @N−CNT as a promising candidate as a commercial anode for LIBs.
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