LiMn0.8Fe0.2PO4@C cathode prepared via a novel hydrated MnHPO4 intermediate for high performance lithium-ion batteries

被引:16
作者
Zeng, Taotao [1 ,2 ]
Liu, Dai-Huo [2 ,3 ]
Fan, Changling [1 ,4 ]
Fan, Runzheng [1 ]
Zhang, Fuquan [1 ,4 ]
Liu, Jinshui [1 ,4 ]
Yang, Tingzhou [2 ]
Chen, Zhongwei [2 ]
机构
[1] Hunan Univ, Coll Mat Sci & Engn, Changsha 410082, Peoples R China
[2] Univ Waterloo, Waterloo Inst Nanotechnol, Waterloo Inst Sustainable Energy, Dept Chem Engn, Waterloo, ON N2L 3G1, Canada
[3] Henan Normal Univ, Collaborat Innovat Ctr Henan Prov Green Mfg Fine C, Sch Chem & Chem Engn, Key Lab Green Chem Media & React, Xinxiang 453007, Peoples R China
[4] Hunan Univ, Hunan Prov Key Lab Adv Carbon Mat & Appl Technol, Changsha 410082, Peoples R China
基金
加拿大自然科学与工程研究理事会; 中国博士后科学基金; 中国国家自然科学基金;
关键词
ELECTROCHEMICAL PERFORMANCE; LIMNPO4/C; PRECURSOR; COMPOSITES; NANOFIBERS; ROUTE;
D O I
10.1039/d2qi02306g
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
With the rapid development of global electro-mobility and the impact of the Russian-Ukrainian war, the increasing cobalt and nickel prices have resulted in supply chain issues for the lithium-ion battery industry. Several types of cathode materials based on low-cost metals, such as manganese and iron, have been widely studied for lithium-ion batteries. Herein, a well-crystallized LiMn0.8Fe0.2PO4@C cathode with a homogeneous structure is synthesized using hydrated MnHPO4 as the precursor. Due to the synergistic effect of oxalic acid on the chelation and reduction of transition metals, a highly stable intermediate hydrated MnHPO4 is constructed, which exhibits a similar structure to LiMnPO4, further promoting the structural transformation from MnHPO4 to LiMnPO4. The obtained LiMn0.8Fe0.2PO4@C exhibits a high electrical conductivity of 6.823 x 10(-2) S cm(-1) and excellent cycling stability with a capacity retention of 98.62% after 200 cycles. This work provides a scalable route for the design of low-cost and high-performance cathode materials for commercial lithium-ion batteries.
引用
收藏
页码:1164 / 1175
页数:12
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