材料科学
纳米棒
阳极
碳化
硫化
纳米颗粒
多孔性
化学工程
纳米结构
纳米技术
碳纤维
储能
电极
扫描电子显微镜
硫黄
复合材料
冶金
复合数
化学
工程类
功率(物理)
物理
物理化学
量子力学
作者
Limin Zhou,Kai Zhang,Jinzhi Sheng,Qinyou An,Zhanliang Tao,Yong‐Mook Kang,Jun Chen,Liqiang Mai
出处
期刊:Nano Energy
[Elsevier]
日期:2017-04-01
卷期号:35: 281-289
被引量:252
标识
DOI:10.1016/j.nanoen.2017.03.052
摘要
Abstract Considering inherent large structural deterioration of conversion-type anode materials during repeated sodiation/desodiation process, the ingenious integration of both nanostructure engineering and chemical hybridization is highly desirable and challenging. Here, ultrafine CoS nanoparticles embedded in porous carbon nanorods (denoted as 7-CoS/C) were facilely fabricated via simultaneous in-situ carbonization and sulfidation of Co-metal organic frameworks (Co-MOF) and have been applied as anode materials for sodium-ion batteries (SIBs). Benefiting from the advantageous embedding architecture between the nanoparticles and porous nanorods, the 7-CoS/C delivers long-term cycling stability (542 mAh g−1 after 2000 cycles with a capacity retention of 91.4% at 1 A g−1) and excellent rate performance (discharge capacities of 510 mAh g−1 at 5 A g−1 and 356 mAh g−1 even at 40 A g−1), which is proved to be characterized of partial pseudocapacitive behaviors during the sodiation/desodiation process. In addition, Na3V2(PO4)3/7-CoS/C full cell with excessive amount of Na3V2(PO4)3 has been assembled and exhibits a capacity of 352 mAh g−1 at 0.5 A g−1. This meaningful approach can be extended to build embedded porous structure of other hybrid composites for next-generation energy-storage technology.
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