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Binder-free tin (IV) oxide coated vertically aligned carbon nanotubes as anode for lithium-ion batteries
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Jungjohann, Katherine L.
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Sandia Natl Labs, Ctr Integrated Nanotechnol, Albuquerque, NM 87185 USA Florida Int Univ, Dept Phys, Miami, FL 33199 USA

Nwanno, Chinaza E.
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Florida Int Univ, Dept Phys, Miami, FL 33199 USA Florida Int Univ, Dept Phys, Miami, FL 33199 USA

Zhang, Jiandi
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Louisiana State Univ, Dept Phys & Astron, Baton Rouge, LA 70803 USA Florida Int Univ, Dept Phys, Miami, FL 33199 USA

Wang, Chunlei
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Florida Int Univ, Dept Mech & Mat Engn, Miami, FL 33174 USA Florida Int Univ, Dept Phys, Miami, FL 33199 USA

Gao, Hongwei
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Montana State Univ, Dept Elect & Comp Engn, Bozeman, MT 59717 USA Florida Int Univ, Dept Phys, Miami, FL 33199 USA

Li, Wenzhi
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Florida Int Univ, Dept Phys, Miami, FL 33199 USA Florida Int Univ, Dept Phys, Miami, FL 33199 USA
机构:
[1] Florida Int Univ, Dept Phys, Miami, FL 33199 USA
[2] Florida Int Univ, Dept Mech & Mat Engn, Miami, FL 33174 USA
[3] Montana State Univ, Dept Elect & Comp Engn, Bozeman, MT 59717 USA
[4] Louisiana State Univ, Dept Phys & Astron, Baton Rouge, LA 70803 USA
[5] Sandia Natl Labs, Ctr Integrated Nanotechnol, Albuquerque, NM 87185 USA
基金:
美国国家科学基金会;
关键词:
Lithium-ion batteries (LIBs);
Vertically aligned CNTs;
SnO;
2;
nanoparticles;
Binder-free anode;
Electrochemical impedance spectroscopy (EIS);
LI-ION;
SNO2;
NANOPARTICLES;
SONOCHEMICAL SYNTHESIS;
NATURAL GRAPHITE;
DIRECT GROWTH;
STORAGE;
COMPOSITES;
ELECTRODE;
SPECTROSCOPY;
STABILITY;
D O I:
10.1016/j.jpowsour.2024.235697
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Despite the tremendous potential of tin oxide (SnO2) as an anode material, irreversible capacity loss due to the sluggish kinetics and structural pulverization as a result of the substantial volume alteration during redox reactions limits its use in lithium-ion batteries. The typical layered design of an electrode consisting of binder and conductive additive can lower the practical capacity of high-capacity electrode materials. We synthesized a binder and conductive additive-free, self-standing core-shell vertically-aligned carbon nanotubes (VACNTs)-SnO2 anode (SnO2-VACNTs) on 3D nickel foam using plasma-enhanced chemical vapor deposition and wet chemical method. The SnO2-VACNTs exhibited excellent cyclability with a specific capacity of 1512 mAh g- 1 at 0.1 A g- 1 after 100 cycles and 800 mAh g- 1 at 1 A g- 1 after 200 cycles. The ultra-fine SnO2 particles (<5 nm) shortened the Li+ diffusion paths into the bulk electrode and alleviated the volume alteration by lowering the strains during the redox reactions. Also, proper inter-tube distance between individual SnO2-VACNTs buffered the volume instability and offered better electrolyte accessibility. Direct connection of VACNTs with the current collector ensured an uninterrupted electron conducting path between the current collector and active material, thus of- fering more efficient charge transportation kinetics at the electrode/electrolyte interfaces.
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h-index: 0
机构:
Max Planck Inst Colloids & Interfaces, D-14476 Golm, Germany Max Planck Inst Solid State Res, D-70569 Stuttgart, Germany