In Situ Generation of Few-Layer Graphene Coatings on SnO2-SiC Core-Shell Nanoparticles for High-Performance Lithium-Ion Storage

被引:248
作者
Chen, Zhongxue [1 ]
Zhou, Min [1 ]
Cao, Yuliang [1 ,2 ]
Ai, Xinping [1 ]
Yang, Hanxi [1 ]
Liu, Jun [2 ]
机构
[1] Wuhan Univ, Coll Chem & Mol Sci, Hubei Key Lab Electrochem Power Sources, Wuhan 430072, Peoples R China
[2] Pacific NW Natl Lab, Richland, WA 99352 USA
基金
美国国家科学基金会;
关键词
tin oxide; few-layer graphene; conversion reactions; core-shell nanostructures; lithium-ion batteries; ELECTROCHEMICAL LITHIATION; ELECTRODE MATERIALS; AMORPHOUS OXIDE; ANODE MATERIAL; BATTERIES; CAPACITY; CARBON; TIN; COMPOSITE; NANOSTRUCTURES;
D O I
10.1002/aenm.201100464
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
A simple ball-milling method is used to synthesize a tin oxide-silicon carbide/few-layer graphene core-shell structure in which nanometer-sized SnO2 particles are uniformly dispersed on a supporting SiC core and encapsulated with few-layer graphene coatings by in situ mechanical peeling. The SnO2-SiC/G nanocomposite material delivers a high reversible capacity of 810 mA h g-1 and 83% capacity retention over 150 charge/discharge cycles between 1.5 and 0.01 V at a rate of 0.1 A g-1. A high reversible capacity of 425 mA h g-1 also can be obtained at a rate of 2 A g-1. When discharged (Li extraction) to a higher potential at 3.0 V (vs. Li/Li+), the SnO2-SiC/G nanocomposite material delivers a reversible capacity of 1451 mA h g-1 (based on the SnO2 mass), which corresponds to 97% of the expected theoretical capacity (1494 mA h g-1, 8.4 equivalent of lithium per SnO2), and exhibits good cyclability. This result suggests that the core-shell nanostructure can achieve a completely reversible transformation from Li4.4Sn to SnO2 during discharging (i.e., Li extraction by dealloying and a reversible conversion reaction, generating 8.4 electrons). This suggests that simple mechanical milling can be a powerful approach to improve the stability of high-performance electrode materials involving structural conversion and transformation.
引用
收藏
页码:95 / 102
页数:8
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