LiFePO4/C nanocomposites for lithium-ion batteries

被引:214
作者
Eftekhari, Ali [1 ,2 ]
机构
[1] Univ Ulster, Engn Res Inst, Newtownabbey BT37 0QB, North Ireland
[2] Queens Univ Belfast, Sch Chem & Chem Engn, Stranmillis Rd, Belfast BT9 5AG, Antrim, North Ireland
关键词
Lithium iron phosphate; LiFePO4/C; Lithium-ion battery; Cathode material; Core-shell; Pseudocapacitance; CARBON-COATED LIFEPO4; IMPROVED ELECTROCHEMICAL PERFORMANCE; REDUCED GRAPHENE OXIDE; MULTISCALE ELECTRONIC TRANSPORT; NANO-SIZED LIFEPO4/C; CORE-SHELL STRUCTURE; CATHODE MATERIAL; SOLVOTHERMAL SYNTHESIS; HYDROTHERMAL SYNTHESIS; PARTICLE-SIZE;
D O I
10.1016/j.jpowsour.2017.01.080
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
LiFePO4, as the most famous member of the family of olivine-type lithium transition metal phosphates, is one of the promising candidates for the cathodes of lithium-ion batteries. However, its battery performance is limited by its low electrical conductivity and slow Li solid-state diffusion. Various methods have been attempted to improve the battery performance of lithium iron phosphate. Among them, compositing the LiFePO4 with carbon nanomaterials seems to be the most promising, as it is facile and efficient. Carbon nanomaterials usually serve as a conductive agent to improve the electrical conductivity while increasing the material porosity in which the solid-state diffusion distances are significantly shortened. Owing to the popularity of various carbonaceous nanomaterials, there is no straightforward line of research for comparing the LiFePO4/C nanocomposites. This review aims to provide a general perspective based on the research achievements reported in the literature. While surveying the research findings reported in the literature, controversial issues are also discussed. The possible contribution of pseudo capacitance as a result of functionalized carbon or LiFePO4 lattice defects is described, since from a practical perspective, a LiFePO4/C electrode can be considered as a supercapacitor at high C rates (with a specific capacitance as large as 200 F g(-1)). The Li diffusion in LiFePO4 has not been well understood yet; while the Li diffusion within the LiFePO4 lattice seems to be quite fast, the peculiar interfacial electrochemistry of LiFePO4 slows down the diffusion within the entire electrode by a few orders of magnitude. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:395 / 411
页数:17
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