In situ magnesiothermic reduction synthesis of a Ge@C composite for high-performance lithium-ion batterie anodes

被引:0
|
作者
Huu, Ha Tran [1 ]
Nguyen, Ngoc Phi [1 ]
Ngo, Vuong Hoang [1 ]
Luc, Huy Hoang [2 ]
Le, Minh Kha [3 ]
Nguyen, Minh Thu [3 ]
Le, My Loan Phung [3 ]
Kim, Hye Rim [4 ]
Kim, In Young [4 ]
Kim, Sung Jin [4 ]
Tran, Van Man [3 ]
Vo, Vien [1 ]
机构
[1] Quy Nhon Univ, Fac Nat Sci, 170 An Duong Vuong, Quy Nhon 55000, Binh Dinh, Vietnam
[2] Hanoi Natl Univ Educ, Fac Phys, 136 Xuan Thuy, Hanoi 11300, Vietnam
[3] Viet Nam Natl Univ Ho Chi Minh City, Univ Sci, Appl Phys Chem Lab, Ho Chi Minh City 70000, Vietnam
[4] Ewha Womans Univ, Dept Chem & Nanosci, Seoul 120750, South Korea
来源
关键词
Ge anode; in situ synthesis; lithium-ion batteries; magnesiothermic reduction; GERMANIUM NANOPARTICLES; ENERGY; SILICON; CARBON; STORAGE; NANOTUBES; HYBRIDS; SYSTEM; MATRIX; ROUTE;
D O I
10.3762/bjnano.14.62
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Metallothermic, especially magnesiothermic, solid-state reactions have been widely applied to synthesize various materials. However, further investigations regarding the use of this method for composite syntheses are needed because of the high reactivity of magnesium. Herein, we report an in situ magnesiothermic reduction to synthesize a composite of Ge@C as an anode material for lithium-ion batteries. The obtained electrode delivered a specific capacity of 454.2 mAh & BULL;g-1 after 200 cycles at a specific current of 1000 mA & BULL;g-1. The stable electrochemical performance and good rate performance of the electrode (432.3 mAh & BULL;g-1 at a specific current of 5000 mA & BULL;g-1) are attributed to the enhancement in distribution and chemical contact between Ge nanoparticles and the biomass-based carbon matrix. A comparison with other synthesis routes has been conducted to demonstrate the effectiveness of contact formation during in situ synthesis.
引用
收藏
页码:751 / 761
页数:11
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