机构:
China Acad Engn Phys, New Mat R&D Ctr, Inst Chem Mat, Chengdu 621900, Sichuan, Peoples R ChinaChina Acad Engn Phys, New Mat R&D Ctr, Inst Chem Mat, Chengdu 621900, Sichuan, Peoples R China
Cheng, Jianli
[1
]
Wang, Bin
论文数: 0引用数: 0
h-index: 0
机构:
China Acad Engn Phys, New Mat R&D Ctr, Inst Chem Mat, Chengdu 621900, Sichuan, Peoples R China
Fudan Univ, New Energy & Mat Lab, Dept Chem, Shanghai 200433, Peoples R China
Fudan Univ, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R ChinaChina Acad Engn Phys, New Mat R&D Ctr, Inst Chem Mat, Chengdu 621900, Sichuan, Peoples R China
Wang, Bin
[1
,2
,3
]
Park, Cheol-Min
论文数: 0引用数: 0
h-index: 0
机构:
Kumoh Natl Inst Technol, Sch Adv Mat & Syst Engn, Gumi 730701, Gyeongbuk, South KoreaChina Acad Engn Phys, New Mat R&D Ctr, Inst Chem Mat, Chengdu 621900, Sichuan, Peoples R China
Park, Cheol-Min
[4
]
Wu, Yuping
论文数: 0引用数: 0
h-index: 0
机构:
Fudan Univ, New Energy & Mat Lab, Dept Chem, Shanghai 200433, Peoples R China
Fudan Univ, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R ChinaChina Acad Engn Phys, New Mat R&D Ctr, Inst Chem Mat, Chengdu 621900, Sichuan, Peoples R China
Wu, Yuping
[2
,3
]
Huang, Hui
论文数: 0引用数: 0
h-index: 0
机构:
China Acad Engn Phys, New Mat R&D Ctr, Inst Chem Mat, Chengdu 621900, Sichuan, Peoples R ChinaChina Acad Engn Phys, New Mat R&D Ctr, Inst Chem Mat, Chengdu 621900, Sichuan, Peoples R China
Huang, Hui
[1
]
Nie, Fude
论文数: 0引用数: 0
h-index: 0
机构:
China Acad Engn Phys, New Mat R&D Ctr, Inst Chem Mat, Chengdu 621900, Sichuan, Peoples R ChinaChina Acad Engn Phys, New Mat R&D Ctr, Inst Chem Mat, Chengdu 621900, Sichuan, Peoples R China
Nie, Fude
[1
]
机构:
[1] China Acad Engn Phys, New Mat R&D Ctr, Inst Chem Mat, Chengdu 621900, Sichuan, Peoples R China
[2] Fudan Univ, New Energy & Mat Lab, Dept Chem, Shanghai 200433, Peoples R China
[3] Fudan Univ, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R China
[4] Kumoh Natl Inst Technol, Sch Adv Mat & Syst Engn, Gumi 730701, Gyeongbuk, South Korea
By using carbon nanotubes (CNTs) as a shape template and glucose as a carbon precursor and structure-directing agent, CNT@Fe3O4@C porous core/sheath coaxial nanocables have been synthesized by a simple one-pot hydrothermal process. Neither a surfactant/ligand nor a CNT pretreatment is needed in the synthetic process. A possible growth mechanism governing the formation of this nanostructure is discussed. When used as an anode material of lithium-ion batteries, the CNT@Fe3O4@C nanocables show significantly enhanced cycling performance, high rate capability, and high Coulombic efficiency compared with pure Fe2O3 particles and Fe3O4/CNT composites. The CNT@Fe3O4@C nanocables deliver a reversible capacity of 1290mAhg(-1) after 80cycles at a current density of 200mAg(-1), and maintain a reversible capacity of 690mAhg(-1) after 200cycles at a current density of 2000mAg(-1). The improved lithium storage behavior can be attributed to the synergistic effect of the high electronic conductivity support and the inner CNT/outer carbon buffering matrix.