Controllable synthesis of LiFePO4 in different polymorphs and study of the reaction mechanism

被引:27
作者
Guo, Hua [1 ,2 ]
Ping, He [1 ]
Hu, Jiangtao [1 ]
Song, Xiaohe [1 ]
Zheng, Jiaxin [1 ]
Pan, Feng [1 ]
机构
[1] Peking Univ, Shenzhen Grad Sch, Sch Adv Mat, Shenzhen 518055, Peoples R China
[2] Stockholm Univ, Dept Mat & Environm Chem, SE-10691 Stockholm, Sweden
基金
中国国家自然科学基金;
关键词
ASSISTED SOLVOTHERMAL SYNTHESIS; RECHARGEABLE LITHIUM BATTERIES; LI-ION BATTERIES; CATHODE MATERIALS; PHASE-TRANSITION; LOW-TEMPERATURE; LIMPO4; M; PRESSURE; NANOPARTICLES; NANOCRYSTALS;
D O I
10.1039/c7ta03369a
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
Lithium iron phosphate, a widely used cathode material in Lithium Ion Batteries (LIBs), crystallizes typically in an olivine-type phase, alpha-LiFePO4 (aLFP). However, the new phase beta-LiFePO4 (bLFP), which can be transformed from aLFP at high temperature with high pressure, can be produced through a simple liquid-phase reaction. The mechanism of controllable synthesis of the two polymorphs of lithium iron phosphate has not been studied thoroughly. In this paper, with thorough experiments, we demonstrate that controllable synthesis of LFP with different crystal polymorphs can be obtained by controlling certain conditions. The phosphoric acid ratio in the reactants and the reaction time play key roles in the controllable syntheses. Higher phosphoric acid ratios and shorter reaction times would result in a higher bLFP content, while a lower amount of phosphoric acid and a longer reaction time would be beneficial to aLFP formation. To illustrate the mechanism for this phenomenon, the detailed reaction process was researched via X-ray diffraction, from which a possible mechanism associated with the evolution of crystal structures was demonstrated. The solvent content is also important for the process: some water content would lead to nanoplate-shaped aLFP particles appearing. Their influence on the reaction could be attributed to the change of thermodynamics and kinetics, which leads to different crystal nucleation, growth and phase-change processes.
引用
收藏
页码:14294 / 14300
页数:7
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