Synthesis of LiMn0.8Fe0.2PO4 Mesocrystals for High-Performance Li-Ion Cathode Materials

被引:22
作者
Wi, Sungun [1 ,2 ]
Kim, Jaewon [1 ,2 ]
Lee, Sangheon [1 ,2 ]
Kang, Joonhyeon [1 ,2 ]
Kim, Kyung Hwan [1 ,2 ]
Park, Kimin [1 ,2 ]
Kim, Kunsu [1 ,2 ]
Nam, Seunghoon [3 ]
Kim, Chunjoong [4 ]
Park, Byungwoo [1 ,2 ]
机构
[1] Seoul Natl Univ, Dept Mat Sci & Engn, WCU Hybrid Mat Program, Seoul 08826, South Korea
[2] Seoul Natl Univ, Res Inst Adv Mat, Seoul 08826, South Korea
[3] KIMM, Dept Nano Mech, Nano Mech Syst Res Div, Daejeon 34103, South Korea
[4] Chungnam Natl Univ, Dept Mat Sci & Engn, Daejeon 34134, South Korea
基金
新加坡国家研究基金会;
关键词
Mesocrystal; Lithium Manganese Iron Phosphate; Carbon Coating; ELECTROCHEMICAL PERFORMANCE; ELECTRODE MATERIAL; PARTICLE-SIZE; LIFEPO4; LIMNPO4; MICROSPHERES; COMPOSITES; SNO2; NANOCOMPOSITE; NANOPARTICLES;
D O I
10.1016/j.electacta.2016.09.005
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The micron-sized LiMn0.8Fe0.2PO4 (LMFP) mesocrystals with high volumetric density were successfully synthesized via a solvothermal method. The LMFP mesocrystals, composed of similar to 30-nm-sized nanocrystallites, exhibit a high tap density of similar to 1.2 g/cm(3). The synthesis of such nano-sized crystals was rendered by ascorbic acid which serves as surface-energy modifier. Interestingly, the ascorbic acid also directed the primary nanocrystals to anisotropic aggregations, and the growth mechanisms were rationally identified by TEM and x-ray diffraction. For reversible Li insertion/extraction, the interconnected particles within the mesocrystals were coated by conductive carbon, and the enhancement of the electrochemical properties (i.e. high specific capacity and good rate capability) was assessed by galvanostatic cycling. We believe that this work provides one of the routes to design electrochemically-favorable meso/nano-structures, which is of great potential for improving the battery performance by tuning the morphology of particles at the multi-length scale. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:203 / 210
页数:8
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